Darkfield Microscopy

FUNGUS
The species specific understanding of, and difference between bacterial phase and fungal phase developments in blood pictures.

©Copyright 1997 by Michael Coyle, Petaluma, California, USA
(Explore Issue: Volume 8, Number 3)

Diseases of the skin, digestive organs, urogenitary tract, mouth, etc. are caused by the multiplication and spread of fungal microorganisms known as mycelia. Mycoses (fungal infections) range in degree from unnoticed to fatal. They are directly related to asthma and allergic alveolitis reactions. They are dealt with by the immune system and competition from other microbes or earlier developmental phases of their own cyclogeny.

Fungal infections can be classified as;

Superficial -- those that effect hair, skin, nostrils, genitals, and oral mucosa

Subcutaneous -- those which occur beneath the skin

Deep -- those which effect the internal organs, lungs, liver, bones, lymph, brain, heart, and urinary tract

These infections often occur in those on long-term antibiotic therapies, corticosteroids, and immunosuppressant drugs. This type of opportunistic infection is common in those with the acquired immunodeficiency syndrome, commonly known as AIDS, and also CFIDS (chronic fatigue syndrome).

Primitive bacterial varlents (thecits)
Some of these fungal forms are received from the environment, are transmitted sexually, or are transmitted through mother's milk (Candida albicans). Candida remains in non-virulent phases of development until the terrain allows for its progression into more complex pathogenic forms. The efficacy of many of the SANUM fungal remedies is based on the sexual activity of the particular species of microorganisms (and/or the benign effect altogether, through competition, on the terrain) which is initiated through the process of reinstalling the microbial flora in the body in it's apathogenic earlier phases of development.

The flora that was installed then copulates with the pathogenic variety and shares the sexual information of the earlier phases, which, all things being equal (terrain modulation, removal of stressors, proper diet, lifestyle, etc.) causes the pathogenic form to convert or be reduced to the apathogenic variety. It is believed that the pathogens are also reduced in valence through the actual activity of the copulatory process.

The main causes of pathogenic albicans overgrowth are indiscriminate antibiotic application and dental inclusions from mercury tooth amalgams. Other factors include addictions to coffee, chocolate, drugs, unsafe sexual pratices, immuncompromisation, stress, chemicals, radiation, improper diet, etc.

The fungal overgrowth occurs because its natural competitors have been removed, in the case of antibiotic usage. In the case of dental amalgams or metals, it is due to decreased immunity from immunocompromisation. The candida also adsorbs the mercury in the gut, thereby serving the function of keeping it from moving deeper in the system, to some degree. A good inclusion in a program of remedies for alleviation of mercury toxicity in the nervous system and brain is broken cell wall chlorella, because not only is it similar to the fungus in that it adsorbs the mercury, but also carries it away. Continue reading >>

Polymorphic Symbionts as Potential Cofactors in Cancer Processes

by Karl Windstosser© Copyright 1997 Explore Publications, Inc. Republished with their permission.
1915
G. Fichera and Citelli (Milan) described "bacterial form elements" in human tumors; after 1925, this included various developmental phases of these in coccal and rod form. It is not clear whether Fichera produced a therapeutic agent from this -- which he designated as "Oncovaccina" -- or whether this name applied to an extract derived from sheep spleen, thymus, duodenum, lymph glands and bone marrow, which Fichera injected his patients with beginning about 1934.

That would make this researcher -- at about the same time as Niehans -- one of the founders of organocellular or cytoplasmatic therapy, which is based on the empirical fact that sheep are the only mammals that are never (or extremely rarely) infested with cancer and that malignant vaccination tumors are just as unlikely to be transferable to them. This is especially true of the younger animals and lambs. We now know that the spleen, thymus and lymph glands exercise central functions in defensive and regulatory processes.

Somewhat later, Clara Jolles-Fonti (1954) and Guarnieri silently took over Fichera's ideas and therapy and added their own work to it. The ingredients of the preparation were simplified, initially to a combination of liver, spleen and duodenal extracts, and, finally, just liver and spleen. In this form, Permicutan (now biosyn.) took over production from Guarnieri in 1950. One milliliter of the preparation "Factor AF 2 Guarnieri" contains the extract from 7 grams liver and 3 grams spleen. The preparation has earned a good reputation in the field of holistic tumor therapy, despite the omission of the thymus component.
1916
Günther Enderlein (1872-1968), biologist and zoologist, professor and curator at the Zoological Museum of the University of Berlin, first presented his revolutionary reconfiguration of bacteriology (developed during the war years -- he had been an army bacteriologist) to the Society of Friends of Natural-Science Research [Gesellschaft Naturforschende Freunde].

Because of war-related problems, his book Bacterial Cyclogeny. Prolegomena to Investigations into the Structure, Sexual and Asexual Reproduction and Development of the Bacteria, finished in the same year, was not able to be printed and published until 1925. Ever since Cohn (1870) and Koch (1876), bacterial monomorphism had become dogma, even though this idea had at first only had provisional status, to provide a framework for additional research.

Even its promulgators continued to report casually on morphological variants of the microbes they observed -- and, in the foreword to his Bacterial Cyclogeny, Enderlein cites a series of predecessors and contemporaries who agreed with the generally postulated and concretely described process of the developmental cycle. In his tireless studies and interpretations, he found the explanation for many controversial microbial findings -- many first described by him, in part heterogeneous, in part identical -- as well as the key to many hitherto (and to some extent to this day) scientifically unexplained processes in pathogenesis and diseases transmission, healing and immunity.

According to Enderlein, all microbes go through a species-specific cycle, which bacteriological theory accepts as quite self-evident for malaria, but which to this day it resists acknowledging for bacteria and fungi, even though there is no exception in the whole wide world to the law of eternal change and the unity of the macrocosm with the microcosm."Cyclogeny" means the transformation and migration of all pathogenic and apathogenic germs through all phases (valences) from the limits of the visible and smaller -- the viral region -- on through the higher-valence phases of the textbook coccal and rod forms and up to the culminant phases of fungi and their mycelia.

In this, the bacterial nucleus plays an important role, which, though Enderlein was aware of it, was not correctly interpreted as to function. Its reduplication corresponds to the length of the bacterial body. According to Enderlein's "Anartatic Fundamental Law", valence increase depends on the prevailing pH of the blood or tissues. The bacteria multiply -- and this, too, was one of Enderlein's fundamental insights -- either asexually by fission or budding (Auxanogeny) or sexually after preliminary nuclear fusion (Probaenogeny).

The latter is always the prerequisite for phasal development upward or downward. The principle of polymorphism and sexual -- i.e. by means of nuclear fusion -- reproduction of bacteria was confirmed 40 years after Enderlein by the Nobel Prize laureates Lederberg, Taumg and Hayes (cited in Seeger, P. G.: Immune Processes and Cancer [Immungeschehen und Krebs] Semmelweis Verlag, Hoya).

Before Enderlein, Mori (1910) had already supported this idea.Out of the many concepts which Enderlein created for his theory, we can here only mention those which are of specific significance for oncological considerations. But this terminology was necessary and justified, since to go back to the usual terminology of orthodox bacteriology or to the nomenclature of the microbe researchers before Enderlein would only have given rise to more new misunderstandings or misinterpretations.Enderlein designated the smallest and lowest bacterial stage as Protit.

It consists of the bare nucleus (Mych) with no protoplasmic coat (Trophosom). One-dimensional reproduction leads to the formation of extremely fine threadlets, or Filits, two- and three-dimensional reproduction to Symprotits. In all, these 3 phases represent Chondritosis, within which a continuously alternating phase-change takes place. Chondrits are in the virus size range (15-300 nm) and are barely visible in the darkfield. Bacteriophages -- Enderlein's interpretation of which differs radically from the orthodox view -- also belong to this stage.

Bacterial flagella are likewise Filits.Higher developmental stages arise -- always dependent on environmental conditions -- through the formation of double- and multiple-nucleus cells with Trophosomes, in which each reduplication of the nuclei corresponds to the next higher stage, or Valence, of the Endobiont. The Enderleinian terms are, in sequence: Basit, Phytit, Rhabdit, Linit, Ascit, Synascit and -- the highest developmental form (Culminant) -- Amoebit.

This represents the fully-developed fungus with all its typical characteristics, flagellum, mycelium and spore formation.Besides the clarification of these morphological phenomena, Enderlein succeeded in identifying the most important vertebrate (but not invertebrate!) symbiont as Mucor racemosus Fresen 1870 in all of its stages from virus to fungus. In the Chondrit stage (see above), it lives as a physiological and innocuous -- probably in fact even useful -- symbiont in the blood and tissue of healthy people.

However, as soon as the biochemical equilibrium changes, the Chondrits ascend to the higher phases or valences and in the process take on pathogenic characteristics. This applies to all civilization-induced diseases, particularly cancer. One can thus designate it as "obligate Mucor parasitism".Retrograde development from higher to lower valences also takes place exclusively via the sexual route by means of nuclear fusion among Chondrits present in sufficient number. This process is blocked in sick persons.

To this end, Enderlein developed Chondritin, with which a chain-reaction-like retrograde development of the pathogenic valences is set into motion. Dealing with the resulting mass of Protits is furthered with the aid of a serum derived from rabbits injected with higher valences and Protits.The hematological changes associated with phasal and virulence increase manifest themselves -- aside from the rise in pH -- in increased (up to 100%) infestation both of erythrocytes and neutrophilic leukocytes as well as plasma with higher-valence Endobionts which present themselves to the eye morphologically as Symprotits, Symplasts, Basits, Ascits, etc.

The erythrocytes, normally the storage depot of dormant symbionts, often take on the so-called burr-cell form, which the orthodox medical laboratories don't know what to do with. These are the microelements, appearing everywhere and active in full virulence. Some of these developmental stages are illustrated in the excellent photomicrographic reproductions in the two discussed books by Bleker and Haring (p. 15ff).

The anemia which often accompanies preliminary and early stages of malignancies is likewise explainable along these lines. The alert observer will not miss the phantom corpuscles, which only appear in the darkfield and which signalize the progressive Endobiont virulence which drives the destructive process. Now, it must be kept in mind that certain stages of this blood infestation can also appear in cases of other chronic and consumptive diseases, i.e. not just cancer and pre-cancerous processes, for example PcP, Hepatitis, MS, radiation and chemotherapy damage, focal diseases (especially in the teeth) etc. With a balanced alkaline diet, cleansing, holistic change therapy and sensible use of Enderlein preparations, these conditions -- even in cases of incipient or early-stage malignancies -- can often be halted or rolled back.

In 1932, Enderlein discovered the second facultative pathogen (unlike the Mucor symbiosis, however, not physiologically endobiotic), the black-spored mold Aspergillus niger van Tieghen, which, in its entire polymorphism and phase-dependent pathology, is the tuberculosis germ. Fontes (1910) provided the proof of this by transmitting the disease by means of bacterium-free filtrates.

The Chondrit and Basit phases give rise to clinical pictures in man which were given all sorts of names by Enderlein's contemporaries -- such as scrofula, lymphatism, camouflaged tuberculosis (Patromikolas), masked tuberculosis (Willy Bircher), certain rheumatic forms (Poncet), tuberculotoxicosis and paratuberculosis.

These also include Much's granules and Spengler's fragments. Other researchers have dedicated themselves to the therapeutic exploitation of these phenomena; these include Pirquet, Ponndorf and the above-mentioned Spengler (see 1902).The Basit, Linit and Ascit stages of Aspergillus are the short and long rod forms of Sclerothrix tuberculosis Koch 1882, solid and not acid-resistant, whose culturing in all phases from s on up to the spore-forming Aspergillus is described accurately by Enderlein.

For therapizing tubercular and pretubercular diseases, Enderlein recommended various preparations, each available in various strengths, which can be administered subcutaneously, intramuscularly or orally, depending on the clinical picture:
1. Stabilized -- i.e. apathogenic -- Aspergillus or tuberculosis Chondritin with mode of action as described for the Endobiont's Chondritin.

2. The caretta Chondritin as cycle phase of the culturing of Sclerothrix antituberculosis Friedmann 1920, the agent of tuberculosis in the sea turtle Thalassochelis caretta. It is not pathogenic to man, but instead has a therapeutic effect like a homeopathic nosode in cases of human tuberculosis. Friedrich Franz Friedmann, who had to endure many attacks and much defamation in his life, deserves our thanks for his research and development of this therapeutic agent, which has fallen into obscurity only because of the chemotherapeutic treatment of tuberculosis.

3. The vaccines of Sclerothrix tuberculosis Koch, containing higher valences than the Chondritin.
4. The sea turtle tuberculosis vaccine, acid-resistant and non-acid-resistant.
5. The tuberculosis sera of rabbits that have been immunized against Sclerothrix tuberculosis Koch. Mode of action as per the Endobiont sera.
6. For all diseases which are, simultaneously or serially, of an Endobiontic or tuberculous nature, the Pliogen-Chondritin consisting of Mucor and Aspergillus Chondrites.
All of the isopathic preparations developed by Enderlein were produced under his personal supervision in his laboratory in Hamburg/Aumühle until shortly before his death. In 1975, the firm of SANUM-Kehlbeck (Hoya) acquired the production license and took over the business. The old, instructive preparation names were changed and many new agents (not from Enderlein) were added. Information and pertinent literature can be requested from the above-named company or from the associated publishing arm, Semmelweis Verlag.Besides these preliminary research results and their therapeutic consequences for the Mucor and Aspergillus cycles, Enderlein published, after 1937, his ideas concerning the cancer-specific or carcinogenic properties of the higher developmental stages of the Mucor Endobiont.

His argument is structured as follows:
1. Human blood is not sterile, as had been previously assumed, but rather harbors in all cases a minuscule parasite. It had not been discovered previously because it exists there primarily in an unusual and hitherto not described form, namely in the submicroscopic Protit stage. This most primitive developmental stage is of the same size order as viruses, which, according to Enderlein, are likewise to be ascribed to the species-specific cycle.

The apparent sterility of standard blood cultures is explained by the fact that these stages in their parasitical property can only be cultured with great difficulty on artificial culture media, and only develop very slowly and poorly. However, sterilely drawn and incubated blood, or simply in blood maintained at room temperature, develops lively growth after a few weeks.
2. The parasite's life in the erythrocytes can be detected in fresh blood through its germination into free Chondrits or Symprotits in blood serum.
3. The relationship of the infection of the erythrocytes to cancer turns out to depend on the following factors:
a. Number of infected erythrocytes and phantom corpuscles;
b. Number of parasites in each infected erythrocyte;
c. Dynamovalence or size of the erythrocyte inclusions.
4. The bacterial form in the blood demonstrates, by its lively mobility, its existence as a special life-form in native preparation.
5. Free and enclosed (in nucleus or cell plasma) Symprotits and Symprotit barbells can also be found in the tumor, usually in enormous numbers.
6. Bacterial rods are also found -- although seldom -- growing out of the tumor cells.
7. Higher bacterial structural forms such as Cystits, Thecits, etc. can also be culturally obtained in blood (or nutrient glucose broth, etc.) and are massively present in tumors, either free or in cell bodies.
8. In sectioned tumors, one finds the highest forms observed in the human body of the parasite's developmental series, namely as fungal mycelium (Developmental History of the Bacteria [Entwicklungsgeschichte der Bakterien], Vol. 1 Number 3).

Enderlein included an aphorism of Lao-Tse's in some of his studies, which applies precisely to the Bacterial Cyclogeny he created: "When things have unfolded to their fullest development, they always return to their roots."

Publications of Enderlein's Numerous Scientific Writings
All together, they number over 500, of which 377 cover entomological topics in the years 1891 to 1942 -- we can here mention only those which are concerned with Endobiosis research and bacterial polymorphism. A complete listing of these, as well as of the contributions of other authors on the same topic, was put out in the sixties by the AKMON Verlag, at that time situated in Aumühle near Hamburg. In addition, we would like to call attention to the reprints listed here of some of Enderlein's and other pertinent publications, published by the Semmelweis Verlag in Hoya.

· "Basic Elements of the Comparative Morphology and Biology of Bacteria." [Grundelemente der vergleichenden Morphologie und Biologie der Bakterien] Session Reports of the Society of Friends of Natural-Science Research [Sitzungsberichte der Gesellschaft der Naturforschenden Freunde], Berlin 1916 (provisional presentation of the concepts of "Bacterial Cyclogeny").
· "Bacterial Cyclogeny." Prolegomena to Investigations into the Structure, Sexual and Asexual Reproduction and Development of the Bacteria. [Bakterien-Cyclogenie. Prolegomena zu Untersuchungen über Bau, geschlechtliche und ungeschlechtliche Fortpflanzung und Entwicklung der Bakterien] Verlag Walter de Gruyter & Co., Berlin/Leipzig 1925. Reprinted by: Semmelweis Verlag, Hoya 1980.

Translated into French by Dr. G. Langevine, Paris.
· "Concerning the Pliocyclody of Bacteria. The Biological Significance of Bacterial Gonits, Gonidies and Cystits." Lectures, ref. in: Session Reports of the Society of Friends of Natural-Science Research [Sitzungsberichte der Gesellschaft der Naturforschenden Freunde], Berlin 1981.
· "Conclusions from the Definitive Unmasking of Monomorphism as a Specious Dogma." [Folgerungen aus der endgültigen Entlarvung des Monomorphismus als spekulatives Dogma] Archive for the Developmental History of Bacteria [Archiv für Entwicklungsgeschichte der Bakterien] Vol. 1 Nr. 1, p. 162ff. (1933).

· "The End of the Cell's Reign as the Ultimate Biological Unit." [Das Ende der Herrschaft der Zelle als letzte biologische Einheit] Archive for the Developmental History of Bacteria [Archiv für Entwicklungsgeschichte der Bakterien] Vol. 1 Nr. 2, p. 171ff. (1933).[Translated and published in Explore! for the Professional, Volume 6, #1 (1995)]

· "The Cycle of the Cancer Agent, Mucor neoformans." [Der Kreislauf der Krebs-Urhebers, Mucor neoformans] (Doyen 1902) Archive for the Developmental History of Bacteria [Archiv für Entwicklungsgeschichte der Bakterien] Vol. 1 Nr. 8, p. 183ff. (1937).

· "On the Hypotheses Concerning the Parasitical Nature of Oncogenesis on the one Hand and the Knowledge Developed over the Preceding Century and a Half concerning the Parasitical Nature of Cancer on the Other Hand." [Zu den Hypothesen über die parasitŠre Krebsentstehung einerseits und den seit eineinhalb Jahrhunderten entwickelten Erkenntnissen der parasitŠren Krebsnatur andererseits] Folk Medicine 3 [Volksheilkunde] (1949).

· "On the Source of all Chronic Diseases." [Vom Urheber aller chronischen Erkrankungen] Folk Medicine 8 [Volksheilkunde] (1955).

· "On the Nature of Chronic Diseases, Specifically of Cancer and Glandular Cancer." [†ber das Wesen der chronischen Erkrankungen, speziell von Krebs und Drüsenkrebs] Private Clinic and Sanatorium 4 [Privatklinik und Sanatorium] (1955).

Periodicals Edited and Published by Enderlein
· Archive for the Developmental History of Bacteria [Archiv für Entwicklungsgeschichte der Bakterien] Vol. 1 Numbers 1-4; Vol. 2 Nr. 1. Verlag Erna Enderlein, Berlin 1931-1940, AKMON Verlag 1941-1972.

· Immunbiologica. Writings on Immunobiological Methods of Fighting Disease. [Immunbiologica. Schriftenreihe über immunbiologische KrankheitsbekŠmpfung] Vols. 1-4: Siebeneicher Verlag, Berlin/Frankfurt 1946-1950; Vols. 5-6: IBICA Verlag, Aumühle near Hamburg 1954.
· AKMON -- Elements of Complete Health and Akmosophy [AKMON -- Bausteine zur Vollgesundheit und Akmosophie.] Vol. 1/1955; Vol. 2/1957 (both IBICA Verlag, Aumühle near Hamburg); Vol. 3/1959 (AKMON Verlag, Aumühle near Hamburg). This has been reprinted by Semmelweis Verlag, Hoya 1980. It contains 23 articles by Enderlein, 12 by other authors.
· Folia Isopathica. Vol. 1/1961 (improved new edition 1970), AKMON Verlag, Aumühle near Hamburg.
· Relevant titles in the complete bibliography: [12, 17, 32-34, 46, 77, 90, 103, 106, 107, 118, 133, 139, 149, 150, 196, 197-199, 201].

The Nature of the Biological Uniformity of the Bipolar Structure of all Chronic Diseases

By Professor Günther Enderlein, Aumühle/Hamburg Member of the Society for Freedom in Science at Oxford
"Who thinks he found it all aloneis dumber than the lowly stone."- J.W. von GoetheWhen, twenty millennia ago, the ancient Indians carried out the healing of all the chronic diseases - including cancer and tuberculosis - with the urine of the holy, beneficial cattle, this was not a forced illusion dictated by "slogans"; rather, it was (already) a tremendous insight, related in its basic features to natural instinct, whose origin arose from a purposeful activity of the most profound regions of the human brain, which - in the course of even more uncounted millennia before these primeval times - had ascended to this culmination of such logically substantiated actions; this stands head and shoulders above the "slogan dictatorship" of all subsequent (and presumably terminal) Epigones who, since Hippocrates (i.e. in the last 25 centuries, within the time-span of geological periods), have managed to reduce a full panoply of human-culture achievements right down to nothing. For these measures of those primeval cultures accord perfectly with the requirement of an individual researcher with cosmic mental ability right up at the edge of the sudden drop in defensive and mental ability against the bipolar primeval foe from the time of the very origin of all vertebrates, who said: "In order to really be able to heal the sick, one must restore what has been lost." In order words, a replacement of the missing part(s)! This man is the pharmacist Oesterlen, in his Handbuch der Arzneimittellehre [Pharmaceutical Handbook] 7th Ed. 1861, p. 3. And what substances are these, that had already been replaced at that time? Well, domesticated cattle, severely burdened with the Endobiont, the most fearsome part of the bipolar parasite structure - if nothing else, simply leukopathy, whose biologically/parasitologically oriented position in humans between cancer, Hodgkin's disease and Felty's syndrome has been established on the basis of my more thorough blood analysis - use up, as "vegetarian raw-food eaters", unheard-of defensive forces in order to keep at bay the threat to their existence from these primordial parasites. And the decomposition products - that freely leave the host body via the skin, bronchia, intestines and kidneys, since they are no longer interesting parasitically - are, in cattle too, apathogenic primitive phases of the Endobiont (Mucor racemosus Fresen), accordingly the lowest-valence Chondrit stages, as well as the following ultimate primitive forms of life, namely the colloids. These metabolites in turn represent precisely those forms that the endobiontically ailing vertebrate had lost in its illness as a result of being fattened up by being overfed with plant or - infinitely worse, animal - protein. It is exactly these factors that, in the endless eras of defensive struggling against this most fearsome permanent parasite of all vertebrates and man, symbolize the successes of the symbiotic achievement of this defensive struggle, since purely apathogenic functions were forced upon them by just this defensive struggle; for this reason, I gave them the name Regulators. From these four excretion possibilities, the Indians chose the urine of the holy, beneficial cattle. This urine therapy made its way to Europe during Medieval times, and has maintained itself down to the present - despite being relegated to the factors of the so-called "fecal pharmacists" - in part also as autologous urine therapy. Despite the fact that this seems completely justified by the stock of living colloids and very primitive Chondrit stages - and could perhaps even be rounded out by hitherto unknown factors - the therapy, using individually-shipped quantities of living colloids and very primitive Chondrits (in purest form) is, without a doubt, at the least considerably more hygienic. It is definitely understandable if the root cause of the chronic disease complex of the primordial parasite is shifted from a bipolar orientation of Endobiont (Mucor racemosus Fresen) and tuberculosis initiator in the primordial cultures' natural knowledge, over to dietary intake. If the objection is raised from the medical camp that the isopathy of the ancient Babylonians is out of the question for microbe-based diseases, since they had no microscopes, then the reply for the Endobiont itself can be that these important developmental phases of the Endobiont indeed are not visible in the microscope to this day. Vitamins deficiency is also not a causal, but rather at most a conditional factor. And then, when later Bircher-Brenner claims a special sensitivity to dietary toxins of the capillary region in the human body as a cause of chronic diseases, this is also merely a consequence of conditional factors that do not connect up with the root causes - since the root causes are and remain the two bipolarly-oriented and structured primordial parasites. After all, the so-called paracoli bacteria in the intestines are by no means degenerate coli bacteria, but rather bacilli from the Endobiont's metabolites, that form quite normally, even without treatment with living Chondritins, capable of probaenogenetic upward development in the intestinal tract, especially in cancer cases etc., from colloids and the most primitive Chondrit stages on up to the Phytit stage. As bacilli, these Endobiont Phytits are strikingly similar to the coli bacterium. Likewise, dystrophy is just a very small part of the conditional causes, since the primary conditional causes are essentially based in overfeeding with vegetable and animal proteins. Less in the over 1000 cancerogenic factors. Likewise, constitution plays a merely subordinate role, since the greater part of it is lost in the consequences (sequelae) of parasite overfeeding. This is very much the case for the tuberculosis portion of the bipolar structure of the primordial parasite, where also dystrophy is by no means a nonspecific basis and tuberculosis yields no sequelae - as Robert Koch and Edmund Ingber (Buenos Aires) maintain - but rather consequences of the primordial parasite's long-term parasitism, and in fact of the overfeeding of both primordial parasites. (Cf. E. Ingber: "Tuberkulose und Lebensordnung" [Tuberculosis and Lifestyle] in: Diaita, 1st year Vol. 1 1955, pp. 11Ð15.) All of these are the grotesque consequences of "monomorphism/monomorphology" slogans which are the basis for the inaccessibility of the essential nature of the chronic disease complex.
Here is a compilation of some of these "slogan factors":
1. The paracoli bacterium is not a degenerate coli bacterium, but rather the Phytit stage of the Endobiont.
2. The root cause of the infectiousness of filtrates of tubercular material is the tubercle bacillus' Chondrit stage; this was determined back in 1910 by Fontes of Brazil (Cf. Mem. Institut. Oswaldo Cruz, 1, 2, 1910, p. 186).
3. Furthermore, H. Dostal demonstrated the easy transportability of the tubercle bacillus in its coccal form (Basit stage) in liquid-nutrient cultures (cf. Wien. Medizin. Wochenschr. [Viennese Medical Weekly], 60th Year 1910, pp. 2098Ð2100, and 63rd Year 1913).
4. Fibrin is by no means a "protein coagulation" precipitate, but rather the Chondrit dendroid of the Endobiont.
5. Thrombocytes are not blood organelles (platelets); they are Thecits of the Endobiont.
6. Megakaryocytes (Metchnikov) are not normal cell components; rather, due to massive infestation with primitive-phase Endobionts, these cells have lost the ability to fission cell or nucleus. These cells have been forgotten in the studied concentration on the focal problem of cleansing in the marrow of all bones.
7. Polynuclear cell is related to the preceding, except that the nucleus is still capable fission, while the cell itself has lost the capability.
8. The megaloblasts of pernicious anemia are not nucleated erythrocytes, but rather erythrocytes having internal colonies of abnormally distended Endobiont Chondrits (pseudo-nucleus!).
9. Normoblasts, erythrocytes originating in bone marrow, have no nucleus, only a pseudo-nucleus consisting of an Endobiont Chondrit colony.
10. Macrocytes are abnormally enlarged erythrocytes with no pseudo-nucleus, whose enlargement is likewise due to massive infestation by the Chondrit stage of the Endobiont.
11. Peripheral granules of the erythrocytes are not organelles (Schilling), but rather Symprotits of the Endobiont.
12. Peripheral rods of the erythrocytes are not organelles (Schilling), but rather bacterial rods of the bacterial phase of the Endobiont that have developed out of the aforementioned peripheral granules. Later on, they break free and crawl about on the erythrocytes and leukocytes like inchworms (hence the designation "wormlets" by Health Officer Dr. Otto Schmidt of Munich).
13. Also, the globucellular and spindle-cell sarcomas contain no host globular or spindle cells; instead, these represent cross-sectioned (globular) cells and diagonally longitudinally-sectioned (spindle) cells from the mycelia of the Endobiont.
14. Reticulocytes (Heilmeyer) are not erythrocytes with special organelles, but erythrocytes internally infested with Endobiont Chondrit trees.
15. Leukocyte pseudopodia formation (dendrites) (after Bond, London 1924: The Leukocyte in Health and Disease, H. K. Lewis & Co.) actually represents Chondrit dendroids of the Endobiont - also identified as "fibrin" by the standard doctrine!
16. The sterility of human blood (in centrifugate and in filtrate). This doctrinal illusion actually represents a massive infestation of all blood elements of all vertebrates (including man) - even the healthiest - with primitive phases of the Endobiont, which infestation develops probaenogenetically on up to the bacterial and even fungal phases as a disease progresses.
17. The sterility of blood serum = the doctrinal illusion as to the contents of the serum as well in the most varied primitive phases of the Endobiont.
18. Diapedesis = the doctrinal illusion concerning the seizure of all protein reserves in the human body by the Endobiont immediately after death, and their formation into "fibrin".
19. The Culminante of the fungal form (Mucor racemosus Fresen) of the Endobiont is easy to obtain by culturing from tumors, as Health Officer Dr. Otto Schmidt of Munich demonstrated as far back as 1903 (and subsequently), and which I have been able to confirm personally.
20. The calcareous coats of the tubercular foci in the lungs are not host defensive processes, but rather manifestations of calcinosis, of the misdirected efforts of the parasite to protect itself from the defensive reactions of human blood.
And added to all this is the awareness, up through Hippocrates, that all the primeval cultures were based from their beginnings on a "true synthesis" of the chronic disease complex - which, although it falsely evaluated the conditional significance of poor diet as causal, nevertheless instinctively traced the unity of the actual root causes to a synthesis pointing to a single disease, namely humoral pathology. But by contrast, after Hippocrates, the illusion of differentiation led to a "pseudo-analysis", i.e. a misinterpretation of a differentiation to a thousand diseases. However, Babylon, Syria and India were able for centuries largely to avoid this mistake, so that the dietary errors that were interpreted as root causal - which of course actually represent conditional causes - they retained as the basis of their viewpoint, as has been maintained in this sense in India to the present, in its purest form among the Hunza tribes in the Karakorum range of northern India. Also, to what extent - coming from an entirely different discipline - is the possibility of a "truly instinctive world-view" taken into account? This from a document from the field of theology: "Now, it is entirely possible that the science of those ancient times already knew some things that our rational science has arrived at by a totally different route. One needs to consider that those ancients obtained their knowledge of the world in a completely different manner; in observing nature, they made use not only of pure reason, but also (in a certain sense) 'contemplative observation'. They were thus in possession of a sensory apparatus and had at their disposal meditative options that were perhaps superior in certain respects to our hyper-rational intellect." (Prof. D. Gerhard von Rad: "Die biblische Schöpfungsgeschichte" [The Biblical Story of Creation]. In: Schöpfungsglaube und Evolutionstheorie [Creationism and Evolutionary Theory]. 1955, p. 36. Alfred Kröner Verlag, Stuttgart.) Now, the unadulterated, unspoiled and slogan-free primeval instincts - as presented to us in the surviving ancient documents - have turned out to be superior in certain such aspects. But that, right down to the present day, the error of a lack of cosmic orientation in biological and comparative-morphological considerations still exists, inasmuch as a descent to the inmost basis of life is neglected when dealing with issues which necessitate a holistic viewpoint, is demonstrated in turn by the research into the "secrets of the germ cell" at the Max Planck Institute in Voldagsen/Hanover. On the basis of the involvement of the cytoplasm of certain plants in the so-called heredity factors, demonstrated by von Wettstein in 1924, who - unlike the genes of the cell nucleus, i.e. the Genome - designated as Plasmone the heredity factors in the cytoplasm. This was followed up by P. Michaelis, to the extent of attempting to find plants in order to make polynuclear crosses with cytoplasm of the other form. And with willow herb from all over the world, after 24 generations (= 24 years) he succeeded, and demonstrated that only the cytoplasm from the maternal cell solely inherits the maternal characteristics. Still, the question as to where in the cytoplasm the germ plasm was to be found could not be observed by this method. But this difficulty is not surprising, since these complications were only observed in isolated hermit cells, and not in highly-potentiated nationalized cellular organizations. Now, this hermit is the Mychit, the primordial cell of the bacteria. This also answers the difficult question, as explained in the article "Das Ende der Herrschaft der Zelle als letzte biologische Einheit" [The End of the Cell's Reign as the Ultimate Biological Unit] (G. Enderlein, in: Archiv für Entwicklungsgeschichte der Bakterien [Archive for the Developmental History of Bacteria], Year I Vol. 2, 2 July 1933, pp. 171Ð179, 5 Illus.) This article confirms, specifically for Microsphaera vaccinae Cohn 1872 (the smallpox pathogen) - through the genesis of the Symprotit to Mychit (the primordial cell) - that the spherical bacterial cell consists of various primitive phases of the microorganism, and hence represents a socialization of these primitive phases. For the very simplest bacterial cell (Mychit), the micrococcal sphere, the nucleus is then the Mych (primordial nucleus) and the plasma the Protitit stage, i.e. the Symprotit (Chondrit stage) and, in the ultimate unit, also the colloid, i.e. the Protit stage. Moreover, the spongiform arrangement is also bound up with it and thus clarified. The so-called "assimilated protein" of the cytoplasm turns out to be an illusion. Thus, one needs to begin at this basal level of phylogeny in order to be able to answer questions of this kind. W. Goethe's cosmic orientation, introduced at the beginning this chapter, also gives us an excellent conclusion for universal questions and issues - particularly, too, for the contrast between holistic knowledge and its collapse for two thousand years to the downfall of humankind of the Epigones: "Microscopes and telescopes actually confuse pure human understanding."J.W. von Goethe, Sprüche in Prosa. Ethisches [Prose Sayings. Ethical]. I, 37

Primitive bacterial variants and cell wall deficient fungal species

Primitive bacterial variants and cell wall deficient fungal species
I begin this section with a quote from "Cell Wall Deficient Forms: Stealth Pathogens" by Lida Mattman.

"Wall-deficient bacteria are called fungoidal as they produce yeast-like (emphasis added) budding spheres or simulate molds with elongated branching threads. (See chondrothecit and free chondrit plates, respectively). How, then, does one solve the dilemma of recognizing a wall-deficient fungus ? One can start with the vital activity in a fungal filtrate of Candida Albicans where the tiny 0.15-µm particles cannot possibly possess the wide hard wall of the parent.

Colonies developing are usually comprised of twisted Gram-negative skeins so delicate that their course is interrupted by submicroscopic gaps. These fine threads of growth have never been described as part of the classic growth of fungi. (Emphasis added where bolded)."
The above description corroborates the findings of Dr. Günther Enderlein when he described such coccoidal manifestations as being either primitive bacterial variants or the most primitive mycelian strands.

Species of microorganisms which exhibit fungal variants in tissue (in vivo) are only microscopically visible in the blood as the most elementary and minute primitive spore forms, ranging in size up from approximately 0.15 microns. The notion that anyone is viewing fungus balls in phase contrast or darkfield is technically a complete misconception, as the forms which are being regarded as fungal developments are appearing in an alkaline milieu in the blood which will not support the fungal stages of development. This is not to say that the microorganisms may not be a species that can represent fungal developments elsewhere in the body.

But this species specificity is indeterminable by viewing the fresh live blood, as there is not a way to distinguish which species is being viewed without culturing it out through the use of a medium, or by aging or heating the sample, under some conditions. This process changes the phase of development into phases that do not appear, again, in the alkaline milieu of the blood. The forms that are being viewed (and mistaken for fungus stage) are actually colloid thecits, thrombocytes, chondrits, ascits, synascits, and mychits, all of which are part of the bacterial phase of development, which develops in an alkaline milieu.

Also, the cell wall deficient forms, chondrits which are symplastic, are mistaken for fungal appearances. These chondrits do represent a fermentative process, but not at the level of a fungal appearance. They are even an earlier stage appearance than the most primitive cell wall mediated bacterial variants. The species, again, are unspecified upon appearance, as they are the same common stages that appear in many species of microorganism developmental cycles.

©Copyright 1997 by Michael Coyle, Petaluma, California, USA(Explore Issue: Volume 8, Number 3)