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Enderlein
Revisiting Enderlein's Perspective in the 21st Century

© Copyright 2001 by Michael Coyle, USA
(Explore Issue: Volume 10, Number 3)

As an individual who provides training in the Enderlein perspective, including the Live or Native Blood Analysis for the health care community, I am in contact with many individuals who are representative of divergent scientific and philosophical backgrounds. The queries that I receive during training sessions are often quite provocative and I have learned to use the three magic words that all good researchers and lecturers must include in their vocabularies. These words are "I don't know," and must be applied judiciously under the appropriate circumstances. I would like to take this opportunity to consider just what we do and do not know regarding Dr. Günther Enderlein's work from today's scientific perspective, with the intention of possibly provoking some consideration on the part of individuals who are interested in the subject.

Here is what we know:

Enderlein was a class A genius. I can personally vouch for the fact that some of what he described morphologically was never viewed by him microscopically, but was an extrapolation that has proven it to be 100% correct due to the advent of such technologies as the scanning electron microscope and the imaging, which is producible thereby.

The conventional laboratory perspective and microscopic imaging equipment that is commonly utilized today does not reveal the majority of the morphological structures that Enderlein described, nor does the scientific community have a working description or perspective for evaluation of those structures when presented with them. It may presume to, but upon closer examination, technicians of that variety must acquiesce and concede to the fact that they are not familiar with the structures, which are viewed, nor their meaning and function.

Polymorphism is a fact, certainly in some species of microorganisms (especially fungal), and is clearly demonstrable microscopically with the proper equipment.

Very little has been done to track the species specificity of these polymorphic variants in and through their varying polymorphic phases of development. The understanding has not been scientifically translated into today's predominant scientific perspective and language, namely genetics. The practical implication of this is that until the DNA sequences have been determined for the complete Cyclogeny as described by Enderlein, the perspective will not enter the mainstream as a 'provable' science, partially due to the fact that it does not translate readily into current scientific terminology.

The Enderlein remedies have a long history of efficacy and provide clinical evidence of the relationship between the isopathic remedy utilized, and the desired observable effect. What this means is that although it hasn't been fully explained or understood exactly why a given remedy works, that it works nevertheless. This also implies that for the practitioner or clinician, there is not a great deal of impetus to create the necessary data to prove the efficacy scientifically. Because these remedies are a product of Nature, pharmaceutical companies, which deal in patentable fractions of Nature, will never likely develop an interest in putting the necessary funds in motion to do the proving.

The disappointing news is that we don't have a working language and perspective that will likely be shared by all in the near future. The good news is that we have a working system for correction of the terrain imbalance that has a long track record of efficacy. A bird in the hand, perhaps?

People sometimes expect me, because I use Enderlein's concepts and discoveries as a platform for my presentations, to be defensive regarding people questioning the paradigm. My actual position is: I would be just as happy to have proven as disproved Enderlein theory as it relates to morphological progressions and their species specificity. I have not seen that evidence in either direction--proof or disproof. What I have seen is the remarkable degree to which the working hypothesis of Enderlein stands for itself. What I have not seen much of is scientific proving to the contrary. A good example of this is that every time that I encounter a naysayer, I ask for a description then of 'just what it is that we are undeniably viewing' in the polymorphic progressions that occur in blood pictures. I have never to this day had anyone claim of "bunkum," a favorite word used to describe "quackery," and give me a reasonable explanation of just what we are looking at. In fact, the majority is even incorrect in the description of the traditionally noted blood elements when viewed in a Darkfield, because they have never seen them that way. This does not stop their jaws from dropping when it is their blood being viewed.

I therefore am equally frustrated due to the lack of affirmation as well as the inability to disprove Enderlein and have that be a step towards proving any other concept. Therefore, I believe that it can be said that the momentum of the times, characterized by the language of DNA, has overshadowed any real desire to even consider rather than dismiss something as compelling as blood examination in the Darkfield.

This tendency towards the function of doubt as a scientific method is always creating the threat of exclusivity of this method in the pursuit of ultimate scientific knowledge, as if such a thing existed. In fact, though, theory evolves constantly and an example of this is the recent disproving of particle theory. So what was proof yesterday turns out to be an outmoded concept today.

In reality though, the reason that Darkfield examination is compelling is that it is equally an art as well as a science. Does the painter know exactly what his creation will look like before he paints it? If he did, why wouldn't he not just make a static copy, a photograph? The painter is seeking the essence or living spirit of the subject, as also is the practitioner performing the living process and dynamic art of Native Blood Evaluation. As the painter may have studied the work of others--technique, blending of colors, preparation of a canvas, and so on, so must the Darkfield practitioner know his stuff, the correct amounts and condition of cells and other numerous factors and then must practice the art of putting all of that together with the profile of the subject. This art may provide the subject of the evaluation with a most important piece of the puzzle towards regaining equanimity, which is a real starting point to work from, and the coaching of an expert who has taken many down the road to recovery. This is much more tangible, compelling and inspiring than a number of sheets of mystified, abstracted numbers, values and terms.

I am constantly amazed that people who are sick will accept a diagnosis, a "naming" of a condition as sufficient! What about what caused and is causing the trouble, and what about a solution that takes everything into account about the condition and the person, rather than attempting to just eliminate the result of the condition?

I would also like to mention before I go further that there is an e-group discussion forum available to practitioners of the art. I highly recommend it, as it is a conversation that is full of feedback from numerous practitioners and is probably one of the best educational formats that you could possibly find for the established practitioner. To become a part of this forum contact the owner of the group, Dr. Rob Abbott at robabbott@gwchem.com and tell him that you saw it here.

Another note of great interest is the development of a National Microscopy Association, which is headed up by Jed Adamson and has recently accomplished the status of a not-for-profit Foundation. This is a membership association for practitioners only with the express intention of organizing research results, establishing a self-governing membership and creating a clarified legal position for practitioners. I can endorse this organization personally, and am a member of it. This non-profit foundation will be instrumental in moving the Enderlein perspective and microscopic blood evaluation altogether into the 21st century, especially at the level of politics and legalities. It is the only non-commerce driven vehicle of its type, which is concentrated in the legal and political arenas and is not an extension of NuLife Sciences or any other commercial organization. Joining this organization will help to assure your right to perform research in the area of live blood analysis and to demonstrate to CLIA and other similar Federal and State organizations our serious intention to be self-governing. For more information on this, contact Jed Adamson at redridege@hotmail.com.

I was recently interviewed by a functionary from the Dept. of Health and Hygiene, which has been commissioned by CLIA to make a recommendation regarding CLIA statutes as they relate to CAM (Complimentary and Alternative Medicine). There is some interest in revising CLIA guidelines to be more reflective of the new understanding of CAM. There was also an expressed interest in not inhibiting research in his area. A report will be available soon on the actual recommendation that was made to CLIA.

(For larger photos click here)

Dry Blood Live Blood
These crystallizations are very low magnification in brightfield (left) and very high magnification in the whiter areas which are puddles of polymerized (unusable) proteins. The crystals in the picture on the right are from the same profile, both of which are a cancer profile. Note the high degree of acidosis. These are both extremely characteristic images of acidosis resulting from Endobiosis.
Crystallizations in live blood. The clearly evident crystals are uric, lactic and citric acids, and possibly others.
Aspergillus niger fern-like crystal. Numerous lymphocytes surround toxic crystals.
 
Blue and blue-green crystals that are colored from prescription drug residues.
Bacterial development in live blood pictures:
Bacterial parasites Bacterial parasites Ascits parasitizing erys Bacterial parasites
Sphaerotilus natans-the sheath will open and release the many small bacterial links Sphaerotilus natans, sheathed bacteria found in sewage and fecal matter
Photos courtesy of Cathy Stotesbury, Arizona Integrative Physicians:
The depicted filamentous free chondrit is approximately 4.5 times the length of the accompanying Red Blood Cells. Copulation is occuring at the top of the image. The moving footage indicates the copulatory effect clearly. After copulation of the nuclei, the chondrit begins to compress and shorten, rapidly leaping into a higher valence. The entire process depicted in the six photos occurs in approximately 2 to 3 seconds.

Now we see that the organism is becoming a tube form with clearly visible nuclei at the top.

The microorganism is now an ascit with a clearly visible nucleus. The effort continues as the ascit becomes denser and more highly developed The total progression is now complete. The ascit is now very dense with clerly discernible nuclei.

 

One more note: NuLife Sciences, Inc., an educationally oriented organization, for which I serve as the Educational Director, is now a research associate of Microsome International, a not-for-profit foundation which operates under Federal and State auspices which allow it to legally perform and disseminate research findings and accept funding for those purposes. Microsome has received research donations at the level of $35,000 to date, but this amount is just a small portion of the funds necessary to accomplish the necessary scientific proving to establish the links between the new genetic understandings and the Enderlein polymorphism, which is the intent of Microsome International. Microsome will be applying for grants and seeking individual and corporate donations to carry out the research into how polymorphism can be understood in the light of the genetic perspective which is predominant today, in order to have this message reach many. All donations are tax-deductible and gratefully welcomed and inquiries can be made by contacting Microsome International directly at 707-781-9558. Financial support from patients who have received help and want to further the availability of the modalities of European Biological Medicine and Enderlein based therapies is an appropriate form of contribution to the research, as well as corporate sponsorship from product development and distribution organizations.

The previous images serve a practical understanding of some of the technical points which are related to both live and dry blood analysis with the hope of furthering and/or reinforcing the understanding of practitioners of the art. These images and descriptions are examples of the content of what is discussed at NuLife Sciences monthly training.

You may contact NuLife Sciences at www.nulifesciences.com or by e-mailing info@nulifesciences.com or phoning 707-781-9557.

Michael Coyle is a Nutritionally Oriented Natural Therapist and Microbiological Researcher who has worked extensively with herbal, homeopathic, isopathic, nutritional, nootropic and energetic therapies. Since 1994, Michael has devoted his time to training medical doctors and complementary health professionals at the NuLife Sciences training facility in Petaluma, CA, in the art and science of native blood evaluation and the associated applications of wholistic therapies. He also has developed two literary source texts; the 430 page Applied Microscopy For Nutritional Evaluation and Correction, an explanation of what Michael has coined "The New Biology," and the accompanying volume The Four Underlying Causes of Illness and What To Do About Them, a treatise on the causative factors underlying illness. Michael is the designer of a breakthrough high resolution, high magnification microscopy system which is ideal for native blood imaging. He is the technical representative and spokesperson for NuLife Sciences, Inc., a corporation created to provide educational services. For additional information on the services offered by NuLife Sciences, Inc. please call 707-781-9557 or access www.nulifesciences.com

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