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| Artifacts of protein polymerization. These are spontaneous morphological factors that develop as a by product of hemolysis. One potential expression of polymerized proteins in a live blood picture. |
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| Crystallization of numerous blood byproducts, including polymerized proteins. Live blood in darkfield at 500X. |
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| The 'lakes' or white areas in this dry blood study indicate degeneration. Their milky appearance is due to the presence of polymerized proteins. These proteins are made unusable through free radical activity in the body and are metabolic waste. |
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In viewing the progressions in the blood, he observed the degradation of more complex morphological structures into less complex structures as they contacted small virus sized particles which he termed spermits. (2). He therefore developed remedies which were composed of the viral sized components of Mucor racemosus and Aspergillus niger, as he presumed that this was identical to what he was observing in the blood. (3, 4, 5) In those days, it was commonly accepted in the scientific community that if something appeared the same, that it was the same. (6) Today these types of determinations are arrived at through DNA or RNA sequencing and/or the analysis of specific proteins.
In Dr. Gerner's experiments, Darkfield Bodies were isolated and cultured and were determined not to be living organisms due to the lack of a plasma membrane. The Darkfield Bodies (whichever were observed , which is not clearly defined in the Ullmann article) also were determined to be primarily composed of albumin and globin, with globin being the primary constituent. Additionally, the Darkfield Bodies did not stain positive for DNA.
If the constant rearrangement of the protein skeleton and plasma membrane of the cell is inhibited, oxidative damage to hemoglobin occurs from the physical stressing of the red corpuscles as they move through the small capillaries, which are smaller than the cells. This produces some of the same phenomenon as the intentional stressing of the specimen through the inclusion of alkaline solution (sodium), and/or physically stressing the cells by applying pressure to the cover slip in the instance of a wet smear (live blood specimen). If the cell has oxidative damage (free-radical effect), it cannot respond to the capillary induced stress quickly enough and the cells then begin to lyse. This lysing effect causes protein polymerization which produces the morphological appearances through clumping and also produces the 'lakes' phenomenon noted in the dry blood evaluation or Heitan-LeGarde screening process. (7) Changes in the cell shape signals elimination from the body by the spleen and liver. A result of this process is the release of unbound hemoglobin into the serum. Finally, as this process proceeds, increasingly greater amounts of protein particles clump and become what has been termed in the Enderlein perspective as symprotits and macrosymprotits, etc., indicators of Dysbiosis.
Summation and Opinion
Regardless of whether or not there is an abscence of DNA in the microorganisms which are viewed in the screening of living blood, it can be stated with conviction that the appearances of the by-products of cellular lysis due to oxidative stress hold many if not most of the same implications regarding physiologic disturbances, from the practitioner's clinical perspective. This factor is reinforced by the certainty that the isopathic preparations, which have been created by Dr. Enderlein and others, exhibit a high degree of efficacy when applied by a properly trained practitioner, as approximately 80 years of clinical application by a high number of advanced biological practitioners will attest. The question would be, how? How do the remedies work if they are not specific to a species which has involvement in the degenerative process? Why, for instance, does a combination Mucor Racemosus/Aspergillus niger product taken as a remedy, have an effect on some Candidiasis conditions, resulting in complete reversal of the morphological imbalances in a blood picture?
The answers are few and the alignment of the morphological information towards the present-day DNA based perspective only creates many new questions. I do not think that there is a single field in CAM (Complementary and Alternative Medicine) that is such an orphan as microbiology, in the first place. With all of the scientific application of this European Biological Medicine perspective for the last 80 years, the only information that is known to have scientific bearing on the DNA relationships to the Darkfield Bodies comes from one research finding? This in a field that is the richest possible ground for scientific advancement, the categorizing and cataloguing of the millions of microorganisms potentially present in a body at any given time, and how they function and thereby effect health. This is more interesting research than stem-cell research, for instance, because it potentially would show you what was causative in the light of microoganism effects on the physiology, whereas stem cell research shows a way to fix the problem (possibly), but still never looks at what is driving it, in life itself, which is the most important information for the practitioner and the subject of therapy. Over the years, I have become increasingly impressed by the evidence, clinical and scientific, that shows that virtually all disease processes have an underlying microorganism counterpart, cause, or component.
