Showing posts with label Enderlein. Show all posts
Showing posts with label Enderlein. Show all posts
Thursday, March 19, 2009
What are Isopathics?
What are Isopathics? Isopathics: these are the original isopathic remedies developed by the German scientist Professor Dr. Günther Enderlein. Read more
Monday, January 19, 2009
Cyclogenie means the transformation and migration of all pathogen and not pathogen germs by all phases (valences)
Cyclogenie means the transformation and migration of all pathogen and not pathogen germs by all phases (valences) of the border of the visibility, and among them the virus range, over the higher valence phases of the text book-in accordance with-eaten Kokken and the staebchen up to the kulminanten phases of the mushrooms and their Myzelien. Read more
Monday, November 17, 2008
After Enderleins research results Fresen all illnesses can develop
After Enderleins research results Fresen all illnesses can develop from the Zyklode of the Mucor racemosus, whose degenerated proteins a direct influence on the blood exercise. These pathogenen forms arranged Enderlein for example impact accumulations, cardiac infarct, disturbances of the blood clotting, Vein disease, hearing fall, as well as rheumatism forms, Thrombocytopenia, cervical syndrome and Osteomyoscleroses determined too. Continue Reading >>
Monday, November 3, 2008
The micro organisms go through themselves a specific cycle into these "Cyclogenie
The micro organisms go through themselves a specific cycle into these "Cyclogenie" changing the Endobionts up to the high-pathological mushroom forms (Kulminante). For the change the environment of the fabric, which is defined by pH values and redox potentials, is decisive.
Furthermore Enderlein stated that by the administration of lower valence forms the higher valence forms develop into their original apathogen form back. Continue Reading >>
Furthermore Enderlein stated that by the administration of lower valence forms the higher valence forms develop into their original apathogen form back. Continue Reading >>
Wednesday, October 29, 2008
What did the research in the Pleomorphismus reach so far?
Dr. W. von Brehmer proved in the year 1932 on the basis the school medical proceeding (5 theories Robert cook) the fact that the bacterial stature form in the blood, mentioned by it Siphonospora is to be regarded polymorpha, as a cause of each cancer illness and received 1932 for its realizations the acknowledgment of realm public health authorities at that time.
Also Professor Dr. G. Enderlein recognized that other stature forms are causal in the blood for a multiplicity at illnesses. Among other things are this diseases such as angina pectoris, cardic infarct, hearing fall, Ulcus curis, in addition, the Tuberculoses and cancer. Continue Reading >>
Also Professor Dr. G. Enderlein recognized that other stature forms are causal in the blood for a multiplicity at illnesses. Among other things are this diseases such as angina pectoris, cardic infarct, hearing fall, Ulcus curis, in addition, the Tuberculoses and cancer. Continue Reading >>
Monday, September 29, 2008
Prof.Enderlein - Pleomorphism
The method involves generating images, outputting the images, comparing specific patterns of an image with known patterns, determining deviations and/or agreements and outputting the results regarding which type of fungus is involved. The generated dark field images are placed in a memory and image data and/or additional information are transmitted by a data transmission device. AN Independent claim is also included for the following: (a) an arrangement, especially for implementing the inventive method.
Tuesday, September 2, 2008
Germs and Viruses. Part 4
In 1898, Guenther Enderlein (1872-1968) graduated with honors in natural sciences, physics and zoology from Leipzig University, and in 1914 he became a bacteriologist and serologist at the German military hospital at Stettin. Enderlein had studied the findings of Antoine Bechamp and had further studied under Rudolph Leuckart, the zoologist who initiated the modern science of parasitology, and also under Otto Schmidt, the doctor who in 1901 reported the discovery of parasites in the blood of cancer patients. (Schmidt was not the first to discover cancer parasites. As early as 1890 Scottish pathologist William Russell reported on widely variegated microbes present in all cancer tissue, which microbes were referred to as "Russell bodies".)
It was in 1916 while studying typhus that Dr Enderlein observed microscopic living entities in blood samples which he called protits, which could move, unite with other microorganisms and disappear. Later on, using dark field microscopy, he observed that these micro-organisms could change in form through a cycle of countless variations, and he also described how different types of protein-based micro-organisms flourished in blood cells and plasma of all animals, representing an essential part of the normal life process.
As part of the normal life process, these microorganisms live together within the body in a mutually beneficial relationship known as symbiosis. However, he noted that with any deterioration of the body's interior environment in which the pH of the blood becomes either acid or strongly alkaline* the normally harmless microbes would begin to change and in stages evolve into forms of a pathogenic nature, just as Bechamp had said. Enderlein recorded these observations in his book Bakterien Cyclogenic (The Life Cycle of Bacteria), published in 1925 (translated from the German by Dr Phillip Hadley), at which time he became a member of the Microbiological Society of Vienna of which he was later to become president. Continue Reading >>
It was in 1916 while studying typhus that Dr Enderlein observed microscopic living entities in blood samples which he called protits, which could move, unite with other microorganisms and disappear. Later on, using dark field microscopy, he observed that these micro-organisms could change in form through a cycle of countless variations, and he also described how different types of protein-based micro-organisms flourished in blood cells and plasma of all animals, representing an essential part of the normal life process.
As part of the normal life process, these microorganisms live together within the body in a mutually beneficial relationship known as symbiosis. However, he noted that with any deterioration of the body's interior environment in which the pH of the blood becomes either acid or strongly alkaline* the normally harmless microbes would begin to change and in stages evolve into forms of a pathogenic nature, just as Bechamp had said. Enderlein recorded these observations in his book Bakterien Cyclogenic (The Life Cycle of Bacteria), published in 1925 (translated from the German by Dr Phillip Hadley), at which time he became a member of the Microbiological Society of Vienna of which he was later to become president. Continue Reading >>
Wednesday, August 27, 2008
A modern scientific perspective on Prof. Dr. Enderlein's concept of microbial life cycles
A modern scientific perspective on Prof. Dr. Enderlein's concept of microbial life cycles
Townsend Letter for Doctors and Patients, May, 2003
In 1925, German zoologist Prof. Dr. Gunther Enderlein published his concepts of microbial life cycles based on blood analysis observations in the book The Life Cycle of Bacteria (Bakterien Cykiogenie). (1) He theorized that the origin of every microbe was a tiny protein of plant origin that Enderlein called protits or colloids. Furthermore, he thought that specific stimuli caused this protein to polymerize from ball-like structures - which he labelled symprotits and macrosymprotits - into spermites, which Enderlein believed was a virus or prestage of bacteria. From this spermite (viral phase), Enderlein reported that further development to a bacterium could take place, with final culmination into the fungi Aspergillus niger or Mucor racemosus.
This paper will report on the molecular identification of so-caled protits, symprotits and macrosymprotits, the initial stages of Enderlein's proposed life cycle of bacteria. Modern research conducted by Dr. Christopher Gerner, PhD in Biochemistry at the University of Vienna, Austria, has shown that these forms are primarily composed of the human body's own molecules, globin and albumin, and do not consist of plantbased proteins as thought by Enderlein. In addition, Enderlein did indeed observe some microscopic phenomena that seem to correlate to illness processes in human blood. However, his model of a life cycle of bacteria with a protein of plant origin (protit) as the starting point is no longer viable in light of the presented results. Today's scientific knowledge of living processes are very precise, but were unknown to Enderlein in 1925. Taking into account the limited knowledge and scientific techniques available to Enderlein decades ago, we can better understand how he came to his erroneous theories.
The Life of Prof. Dr. Enderlein
Professor Dr. Gunther Enderlein was born in 1872 in Leipzig, located in eastern Germany. He studied natural science, physics and zoology at the University of Liepzig and graduated summa cum laude. Following graduation, Enderlein served as an assistant at the Agricultural University in Berlin. He married in 1904 and two years later accepted a new position at the Zoological Museum in Stettin. In 1914, the First World War began and Enderlein served as a doctor in a German Military Hospital in Stettin. From 19 16-1922, he conducted research on his theory of bacterial life cycles, and published his findings in a book entitled Bakterien Cyklogenie (The Life Cycle of Bacteria) in 1925. During that period, he also was the director at the Zoological Institute and curator at the Berlin Zoological Museum.
In 1944, Dr. Enderlein founded the microbiological firm IBICA in Berlin. In 1949, he moved the company's headquarters and production facilities to Aumuehle, near Hamburg. In 1968, Enderlein died at the age of 96, and in 1975 the equipment of the IBICA Company was sold. (2)
Beckground to Enderlein's Observation in Blood Samples
In 1916, Dr. Enderlein began his investigations of blood under the microscope. He used techniques available at that time, namely phase contrast and darkfield microscopy. (3) These methods enabled him to observe both stained, dried blood and live blood preparations from healthy and sick animals and humans. (4,5) During his investigations, Enderlein observed many morphologies in the blood that he correlated to illnesses. (6) Enderlein reported seeing ball-like morphologies that he called protits, symprotits and macrosymprotits, depending on their size increase. (7) Moreover, he observed stringlike structures that he called filits, and string-like structures with a ball-like morphology on one end that he named spermites. (8,9)
Ball-like morphologies significantly larger in size than symprotits and macrosymprotits were called mychit or thecit, (10) while Enderlein named morphologies of many large, ball-like structures assembled in a row basit, phytit, rhabdit, linit and ascit, depending on the number arrayed. (11) Finally, the German researcher identified highly complex morphological structures as systases or petoharphen. (12)
Enderlein observed these morphologies in the blood of patients suffering from various illnesses, and was able to correlate different morphologies to the progress of illnesses. (13) As a result, he concluded that specific pathogenic structures developed in size and appearance depending on the progress of a particular illness (Endobiosis). (14) Enderlein was able to make these structures microscopically invisible by adding alkaline solution to the blood preparation, an effect he could not observe by adding an acidic solution. (15) This made him believe that he was observing a depolymerization reaction that resembles the reversing of the postulated upward development. (16) Because the structures he identified were affected by an alkaline solution and not by an acidic solution, Enderlein concluded that a constant intoxification and high acidic load in the blood leads to ongoing physiological disturbances that manifest in the structures observed in blood preparations.
The so-called mychit, thecit, basit, phytit, rhabdit, linit and ascit structures are morphologically similar to Syncrotis buccalis or Sclerothrix tuberculosis bacteria grown in culture when viewed with phase contrast microscopy. (17) Due to this similarity, Enderlein concluded that these structures observed in blood preparations were living bacteria. (18) Systase structures are morphologically comparable to fungi such as Mucor racemosus or Aspergillus niger grown in liquid culture. (19) Therefore, Enderlein further inferred that systase structures observed in the blood of seriously ill patients are actually the fungi Mucor racemosus and Aspergillus niger. (20) With this insight as background, it is possible to understand how Enderlein came to his conclusions.
Isopathic Remedies Developed By Enderlein
In his laboratory, Enderlein was able to reduce the morphological complexity of Mucor racemosus and Aspergillus niger preparations to ball-like structures with alkaline solution, much like he was able to do with systase morphologies in blood preparations. (21) He concluded that these fungi were the polymerization products of ball-like structures composed of a specific protein of plant origin, the so-called protit. (22)
To better understand Enderlein's ideas, it is important to define the term "isopathic." Samuel Hahnemann (1755-1843), the Father of Homeopathy, coined the terms homeopathy (Greek for homo ion similar, pathos = suffering or disease) and isopathy (Greek for iso = same, pathos = suffering or disease). Homeopathy attempts to restore disrupted functions and life processes of ill patients by prescribing a diluted substance that, when given in large doses, provokes symptoms in a healthy person similar to those exhibited by the ill patient. Homeopathic remedies are typically herbs or minerals. In contrast, isopathy involves treatment with the same substance that causes the illness, such as microbial pathogens or toxins, and additionally includes highly diluted microbes such as gonorrhea, scabies, syphilis or tuberculosis. Because Enderlein understood his remedies as lower, benign forms of the fungi Mucor racemosus and Aspergillus niger, he used the term isopathy to describe the preparations.
Enderlein's Concepts on the Origin of Illnesses
While analyzing blood, Enderlein observed that when so-called spermites interacted with so-called mychits, the morphological structures disappeared. (24) During this period of medical progress in the early 20th century, the viral (bacteriophage) induced lysis or destruction of bacteria recently had been described. (25,26} As a result, Enderlein hypothesized that spermites were viruses that infect mychits, which he believed were bacteria. (27,28) He further thought that spermites induced the degradation of bacterial cells (mychits) to smaller units, namely symprotits and macrosymprotits. Enderlein described this as a sexual process that leads to the transition from pathogenic bacterial forms to non-pathogenic protein forms (symprotit, macrosymprotit) and viral forms (spermites). (29,30)
From these observations, Enderlein developed the idea that small protein units (protits and symprotits) from the fungi Mucor racemosus and Aspergillus niger should be able to induce the downgrading or degradation of pathologic morphologies that he observed in the blood samples of sick people. (31-33) Consequently, Enderlein then produced isopathic remedies made from Mucor racemosus and Asp ergillus niger that he thought provided the apathogenic structures (protits, symprotits and spermites) that supposedly could reduce complex pathogenic structures in the blood of patients suffering from various kinds of illnesses. (34) Source:
Townsend Letter for Doctors and Patients, May, 2003
In 1925, German zoologist Prof. Dr. Gunther Enderlein published his concepts of microbial life cycles based on blood analysis observations in the book The Life Cycle of Bacteria (Bakterien Cykiogenie). (1) He theorized that the origin of every microbe was a tiny protein of plant origin that Enderlein called protits or colloids. Furthermore, he thought that specific stimuli caused this protein to polymerize from ball-like structures - which he labelled symprotits and macrosymprotits - into spermites, which Enderlein believed was a virus or prestage of bacteria. From this spermite (viral phase), Enderlein reported that further development to a bacterium could take place, with final culmination into the fungi Aspergillus niger or Mucor racemosus.
This paper will report on the molecular identification of so-caled protits, symprotits and macrosymprotits, the initial stages of Enderlein's proposed life cycle of bacteria. Modern research conducted by Dr. Christopher Gerner, PhD in Biochemistry at the University of Vienna, Austria, has shown that these forms are primarily composed of the human body's own molecules, globin and albumin, and do not consist of plantbased proteins as thought by Enderlein. In addition, Enderlein did indeed observe some microscopic phenomena that seem to correlate to illness processes in human blood. However, his model of a life cycle of bacteria with a protein of plant origin (protit) as the starting point is no longer viable in light of the presented results. Today's scientific knowledge of living processes are very precise, but were unknown to Enderlein in 1925. Taking into account the limited knowledge and scientific techniques available to Enderlein decades ago, we can better understand how he came to his erroneous theories.
The Life of Prof. Dr. Enderlein
Professor Dr. Gunther Enderlein was born in 1872 in Leipzig, located in eastern Germany. He studied natural science, physics and zoology at the University of Liepzig and graduated summa cum laude. Following graduation, Enderlein served as an assistant at the Agricultural University in Berlin. He married in 1904 and two years later accepted a new position at the Zoological Museum in Stettin. In 1914, the First World War began and Enderlein served as a doctor in a German Military Hospital in Stettin. From 19 16-1922, he conducted research on his theory of bacterial life cycles, and published his findings in a book entitled Bakterien Cyklogenie (The Life Cycle of Bacteria) in 1925. During that period, he also was the director at the Zoological Institute and curator at the Berlin Zoological Museum.
In 1944, Dr. Enderlein founded the microbiological firm IBICA in Berlin. In 1949, he moved the company's headquarters and production facilities to Aumuehle, near Hamburg. In 1968, Enderlein died at the age of 96, and in 1975 the equipment of the IBICA Company was sold. (2)
Beckground to Enderlein's Observation in Blood Samples
In 1916, Dr. Enderlein began his investigations of blood under the microscope. He used techniques available at that time, namely phase contrast and darkfield microscopy. (3) These methods enabled him to observe both stained, dried blood and live blood preparations from healthy and sick animals and humans. (4,5) During his investigations, Enderlein observed many morphologies in the blood that he correlated to illnesses. (6) Enderlein reported seeing ball-like morphologies that he called protits, symprotits and macrosymprotits, depending on their size increase. (7) Moreover, he observed stringlike structures that he called filits, and string-like structures with a ball-like morphology on one end that he named spermites. (8,9)
Ball-like morphologies significantly larger in size than symprotits and macrosymprotits were called mychit or thecit, (10) while Enderlein named morphologies of many large, ball-like structures assembled in a row basit, phytit, rhabdit, linit and ascit, depending on the number arrayed. (11) Finally, the German researcher identified highly complex morphological structures as systases or petoharphen. (12)
Enderlein observed these morphologies in the blood of patients suffering from various illnesses, and was able to correlate different morphologies to the progress of illnesses. (13) As a result, he concluded that specific pathogenic structures developed in size and appearance depending on the progress of a particular illness (Endobiosis). (14) Enderlein was able to make these structures microscopically invisible by adding alkaline solution to the blood preparation, an effect he could not observe by adding an acidic solution. (15) This made him believe that he was observing a depolymerization reaction that resembles the reversing of the postulated upward development. (16) Because the structures he identified were affected by an alkaline solution and not by an acidic solution, Enderlein concluded that a constant intoxification and high acidic load in the blood leads to ongoing physiological disturbances that manifest in the structures observed in blood preparations.
The so-called mychit, thecit, basit, phytit, rhabdit, linit and ascit structures are morphologically similar to Syncrotis buccalis or Sclerothrix tuberculosis bacteria grown in culture when viewed with phase contrast microscopy. (17) Due to this similarity, Enderlein concluded that these structures observed in blood preparations were living bacteria. (18) Systase structures are morphologically comparable to fungi such as Mucor racemosus or Aspergillus niger grown in liquid culture. (19) Therefore, Enderlein further inferred that systase structures observed in the blood of seriously ill patients are actually the fungi Mucor racemosus and Aspergillus niger. (20) With this insight as background, it is possible to understand how Enderlein came to his conclusions.
Isopathic Remedies Developed By Enderlein
In his laboratory, Enderlein was able to reduce the morphological complexity of Mucor racemosus and Aspergillus niger preparations to ball-like structures with alkaline solution, much like he was able to do with systase morphologies in blood preparations. (21) He concluded that these fungi were the polymerization products of ball-like structures composed of a specific protein of plant origin, the so-called protit. (22)
To better understand Enderlein's ideas, it is important to define the term "isopathic." Samuel Hahnemann (1755-1843), the Father of Homeopathy, coined the terms homeopathy (Greek for homo ion similar, pathos = suffering or disease) and isopathy (Greek for iso = same, pathos = suffering or disease). Homeopathy attempts to restore disrupted functions and life processes of ill patients by prescribing a diluted substance that, when given in large doses, provokes symptoms in a healthy person similar to those exhibited by the ill patient. Homeopathic remedies are typically herbs or minerals. In contrast, isopathy involves treatment with the same substance that causes the illness, such as microbial pathogens or toxins, and additionally includes highly diluted microbes such as gonorrhea, scabies, syphilis or tuberculosis. Because Enderlein understood his remedies as lower, benign forms of the fungi Mucor racemosus and Aspergillus niger, he used the term isopathy to describe the preparations.
Enderlein's Concepts on the Origin of Illnesses
While analyzing blood, Enderlein observed that when so-called spermites interacted with so-called mychits, the morphological structures disappeared. (24) During this period of medical progress in the early 20th century, the viral (bacteriophage) induced lysis or destruction of bacteria recently had been described. (25,26} As a result, Enderlein hypothesized that spermites were viruses that infect mychits, which he believed were bacteria. (27,28) He further thought that spermites induced the degradation of bacterial cells (mychits) to smaller units, namely symprotits and macrosymprotits. Enderlein described this as a sexual process that leads to the transition from pathogenic bacterial forms to non-pathogenic protein forms (symprotit, macrosymprotit) and viral forms (spermites). (29,30)
From these observations, Enderlein developed the idea that small protein units (protits and symprotits) from the fungi Mucor racemosus and Aspergillus niger should be able to induce the downgrading or degradation of pathologic morphologies that he observed in the blood samples of sick people. (31-33) Consequently, Enderlein then produced isopathic remedies made from Mucor racemosus and Asp ergillus niger that he thought provided the apathogenic structures (protits, symprotits and spermites) that supposedly could reduce complex pathogenic structures in the blood of patients suffering from various kinds of illnesses. (34) Source:
Thursday, August 14, 2008
Book's recommendation's on the topic Live Blood Cell Darkfield Microscopy
Here some book’s recommendations on the topic Live Blood Cell Analysis Dark field Microscopy:
· Introduction Into Darkfield Diagnostics by Prof. Dr. Gunther Enderlein
· A Comprehensive Guide to Sanum Therapy by Guenther Enderlein
· BIOLOGICAL MEDICINE: THE FUTURE OF NATURAL HEALING by Dr. Thomas Rau
· The Swiss Secret to Optimal Health: Dr. Rau's Diet for Whole Body Healing by Thomas Rau and Susan Wyler
· The Blood and Its Third Element by Antoine Bechamp
· Bechamp or Pasteur? by Ethel, D Hume
· An Introduction to Antoine Bechamp by Douglas Hume
· Blood and its Third Anatomical Element by A. Bechamp
· Bechamp or Pasteur: A Lost Chapter in the History of Biology by Douglas Hume
· The Mystery of Fermentation by Douglas Hume
· Praxis der SANUM-Therapie by Harald Krebs
· Praxisleitfaden SANUM-Therapie nach Prof. Enderlein by Günter WeigelPraxisleitfaden Dunkelfeld-Vitalblutuntersuchung by Günter Weigel more info about this topic Live Blood Cell Analysis Dark field Microscopy at Live Blood Course: Dark field Course Blog and Live Blood Blog.
· Introduction Into Darkfield Diagnostics by Prof. Dr. Gunther Enderlein
· A Comprehensive Guide to Sanum Therapy by Guenther Enderlein
· BIOLOGICAL MEDICINE: THE FUTURE OF NATURAL HEALING by Dr. Thomas Rau
· The Swiss Secret to Optimal Health: Dr. Rau's Diet for Whole Body Healing by Thomas Rau and Susan Wyler
· The Blood and Its Third Element by Antoine Bechamp
· Bechamp or Pasteur? by Ethel, D Hume
· An Introduction to Antoine Bechamp by Douglas Hume
· Blood and its Third Anatomical Element by A. Bechamp
· Bechamp or Pasteur: A Lost Chapter in the History of Biology by Douglas Hume
· The Mystery of Fermentation by Douglas Hume
· Praxis der SANUM-Therapie by Harald Krebs
· Praxisleitfaden SANUM-Therapie nach Prof. Enderlein by Günter WeigelPraxisleitfaden Dunkelfeld-Vitalblutuntersuchung by Günter Weigel more info about this topic Live Blood Cell Analysis Dark field Microscopy at Live Blood Course: Dark field Course Blog and Live Blood Blog.
Tuesday, August 12, 2008
Websites of Interest
Explore Publications (and Explore Magazine)
www.electriciti.com/explore/
Devoted to putting in front of the discriminating public, quality reliable information from the cutting edge of Alternative and Holistic Medicine, Nutritional Therapies, Energy Medicine, Homeopathy and Physics. Explore Magazine is published for the Medical Profession, Scientists, and other serious researchers who are interested in these areas. This site gives a glimpse into the magazine's contents on an ongoing basis. Topics include:; Darkfield; Microscopy; Overunity; Pleomorphism; Catastrophism; Biology; Enderlein Biology; Harmonic Healing; Past Issues; Current Issue; Sample Articles; Health Flash; and more information on Subscriptions.
FUNGUS: The species specific understanding of, and difference between bacterial phase and fungal phase developments in blood pictures.
www.explorepub.com/articles/darkfield.html
Copyright 1997 by Michael Coyle, Petaluma, California, USA. (Explore Issue: Volume 8, Number 3.)
Medical Breakthroughs/Children: Brain Injured Children - Mary of the Light
www.explorepub.com/articles/kane_10_5.html
Copyright 2001 by Patricia Kane, Ph.D., USA. (Explore Issue: Volume 10, Number 5.)
Institute for New Energy
www.padrak.com/ine/
The INE is an official US non-profit technical and membership organization whose monthly newsletter "The New Energy News" reports the latest and up-to-date findings in international New Energy research. The Institute's primary purpose is to promote research and educate society of the importance of alternative energy. The INE bridges the gap between the advanced and fringe scientific technologies being discovered today, and the old and existing scientific paradigms of yesterday. This site includes many outstanding "advanced energy related" papers, reports, summaries, announcements, and web site links that are not found elsewhere.
www.electriciti.com/explore/
Devoted to putting in front of the discriminating public, quality reliable information from the cutting edge of Alternative and Holistic Medicine, Nutritional Therapies, Energy Medicine, Homeopathy and Physics. Explore Magazine is published for the Medical Profession, Scientists, and other serious researchers who are interested in these areas. This site gives a glimpse into the magazine's contents on an ongoing basis. Topics include:; Darkfield; Microscopy; Overunity; Pleomorphism; Catastrophism; Biology; Enderlein Biology; Harmonic Healing; Past Issues; Current Issue; Sample Articles; Health Flash; and more information on Subscriptions.
FUNGUS: The species specific understanding of, and difference between bacterial phase and fungal phase developments in blood pictures.
www.explorepub.com/articles/darkfield.html
Copyright 1997 by Michael Coyle, Petaluma, California, USA. (Explore Issue: Volume 8, Number 3.)
Medical Breakthroughs/Children: Brain Injured Children - Mary of the Light
www.explorepub.com/articles/kane_10_5.html
Copyright 2001 by Patricia Kane, Ph.D., USA. (Explore Issue: Volume 10, Number 5.)
Institute for New Energy
www.padrak.com/ine/
The INE is an official US non-profit technical and membership organization whose monthly newsletter "The New Energy News" reports the latest and up-to-date findings in international New Energy research. The Institute's primary purpose is to promote research and educate society of the importance of alternative energy. The INE bridges the gap between the advanced and fringe scientific technologies being discovered today, and the old and existing scientific paradigms of yesterday. This site includes many outstanding "advanced energy related" papers, reports, summaries, announcements, and web site links that are not found elsewhere.
Sunday, August 3, 2008
Live Blood Analysis
The American medical establishment does not look at live blood. Their practice of staining blood with chemicals kills it. It also kills the ability to really “see” what is going on. But in looking at live blood, you can clearly “see” that there are bacteria, microorganisms and parasites that not only are in the blood, but that over time can grow and can change their shapes. Research has proven that they can become pathogenic (disease producing). This ability of microorganisms to change is the concept of pleomorphism discussed in The Germ Theory of Disease Causation. Understanding this concept is essential to the understanding of cancer and its cure, and the cure of many other diseases.Other researchers have continued along the path blazed by Enderlein and have come to similar findings. Gaston Naessens discovered the protit and watched its life cycle. He calls the protit a “somatid.” Naessens believes this protit/somatid predates DNA and carries on genetic activity. It is the first thing that condenses from light energy, and is the link between light and matter.
Virginia Livingston-Wheeler also researched the protit but called it “progenitor cryptocides.” Progenitor, meaning it existed through millennia, and cryptocides being a cellular killer - essentially the ancestral hidden killer, cancer. Like Naessens, Livingston did some excellent cancer research. Some of her best research was done along with two other women, Eleanor Alexander-Jackson and Irene Diller. They referred to this microbe as the cancer microbe. But in truth it is much more than that. Continue Reading >>
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