TreasureVibe
Member
- Joined
- Jul 3, 2016
- Messages
- 1,941
Biologist Gaston Naessens
President of CERBE inc.
I am the biologist researcher engineer who developed a unique optical instrument, the Somatoscope, capable of observing unstained living matter, allowing me to discover a new particle alive in fresh human blood, that I have called the somatid . Thanks to the discovery of the somatid, at the origin of degenerative diseases, and its importance in many biological functions such as cell division and the transmission of genetic characteristics, I was able to develop the somatidian theory and to bring new responses to diseases affecting the immune system. As the designer, manufacturer and President of CERBE Inc. and CERBE Distribution Inc., I embody the innovative and human vision of health that I propose in my harmonious biological approach which can be curative as well as preventive.
Fundamental research in optics and biology (virology and hematology) have fascinated me for over 60 years, and I actively continue my experiments and development of innovative and non-toxic health products aiming to rebalance the immune system, like 714X. This is my mission in life!
Read more at: Our team | Cerbe Distribution Inc
The Earthshaking Discoveries of Gaston Naessens:
(This book and its Appendixes comprise important reading material that will help you understand "The Life Processes Here on Planet Earth". — Tommy)
Chapter 1
Discovery of the World's Smallest Living Organism
"When the great innovation appears, it will almost certainly be in a muddled, incomplete, and confusing form ... for any speculation, which does not at first glance look crazy, there is no hope."
Freeman Dyson, Disturbing the Universe
Early in the morning of 27 June 1989, a tall, bald French-born biologist of aristocratic mien walked into the Palais de Justice in Sherbrooke, Quèbec, to attend a hearing that was to set a date for his trial. On the front steps of the building were massed over one hundred demonstrators, who gave him an ovation as he passed by.
The demonstrators were carrying a small forest of laths onto which were glued, stapled, or thumbtacked placards and banners. The most eye-catchingly prominent among these signs read: "Freedom of Speech, Freedom of Medical Choice, Freedom in Canada!" "Long Live Real Medicine, Down With Medical Power!" "Cancer and AIDS Research in Shackles While a True Discoverer is Jailed!" "Thank you, Gaston, for having saved my life!" And, simplest of all: "Justice for Naessens!"
Late one afternoon, almost a month earlier, as he arrived home at his house and basement laboratory just outside the tiny hamlet of Rock Forest, Quèbec, Gaston Naessens had been disturbed to see a swarm of newsmen in his front yard. They had been alerted beforehand – possibly illegally – by officers of the Suretè, Quèbec's provincial police force, who promptly arrived to fulfill their mission.
As television cameras whirred and cameras flashed, Naessens was hustled into a police car and driven to a Sherbrooke jail, where, pending a preliminary court hearing, he was held for twenty-four hours in a tiny cell under conditions he would later describe as the "filthiest imaginable." Provided only with a cot begrimed with human excrement, the always elegantly dressed scientist told how his clothes were so foul smelling after his release on ten thousand dollars' bail that, when he returned home, his wife, Françoise, burned them to ashes.
It was to that same house that I had first come in 1978, on the recommendation of Eva Reich, M.D., daughter of the controversial psychiatrist-turned-biophysicist Wilhelm Reich, M.D. A couple of years prior to my visit with Eva, I had researched the amazing case of Royal Raymond Rife, an autodidact and genius living in San Diego, California, who had developed a `Universal Microscope" in the 1920s with which he was able to see, at magnifications surpassing 30,000-fold, never-before-seen microorganisms in living blood and tissue.*
*"What Has Become of the Rife Microscope?," New Age Journal, (Boston, Massachusetts), 1976. This article has, ever since, been one of the Journal's most requested reprints. It is reproduced in this book as Appendix A. Developments in microscopic techniques have only recently begun to match those elaborated by Naessens more than forty years ago
Eva Reich, who had heard Naessens give a fascinating lecture in Toronto, told me I had another "Rife" to investigate. So I drove up through Vermont to a region just north of the Canadian-American border that is known, in French, as "L'Estrie," and, in English, as `The Eastern Townships." And, there, in the unlikeliest of outbacks, Gaston Naessens and his Quèbec-born wife, Françoise (a hospital laboratory technician and, for more than twenty-five years, her husband's only assistant), began opening my eyes to a world of research that bids fair to revolutionize the fields of microscopy, microbiology, immunology, clinical diagnosis, and medical treatment.
Let us have a brief look at Naessens's discoveries in these usually separated fields to see, step by step, the research trail over which, for the last forty years – half of them in France, the other half in Canada – he has traveled to interconnect them. In the 1950s, while still in the land of his birth, Naessens, who had never heard of Rife, invented a microscope, one of a kind, and the first one since the Californian's, capable of viewing living entities far smaller than can be seen in existing light microscopes.
In a letter of 6 September 1989, Rolf Wieland, senior microscopy expert for the world-known German optics firm Carl Zeiss, wrote from his company's Toronto office: "What I have seen is a remarkable advancement in light microscopy. ... It seems to be an avenue that should be pursued for the betterment of science." And in another letter, dated 12 October 1989, Dr. Thomas G. Tornabene, director of the School for Applied Biology at the Georgia Institute of Technology (Georgia Tech), who made a special trip to Naessens's laboratory, where he inspected the microscope, wrote:
Naessens's ability to directly view fresh biological samples was indeed impressive ... Most exciting were the differences one could immediately observe between blood samples drawn from infected and non-infected patients, particularly AIDS patients. Naessens's microscope and expertise should be immensely valuable to many researchers.
It would seem that this feat alone should be worthy of an international prize in science to a man who can easily be called a twentieth-century "Galileo of the microscope."
With his exceptional instrument, Naessens next went on to discover in the blood of animals and humans – as well as in the saps of plants – a hitherto unknown, ultramicroscopic, subcellular, living and reproducing microscopic form, which he christened a somatid (tiny body). This new particle, he found, could be cultured, that is, grown, outside the bodies of its hosts (in vitro, "under glass," as the technical term has it). And, strangely enough, this particle was seen by Naessens to develop in a pleomorphic (form-changing) cycle, the first three stages of which – somatid, spore, and double spore – are perfectly normal in healthy organisms, in fact crucial to their existence. See figure:
The Somatid Cycle.
Even stranger, over the years the somatids were revealed to be virtually indestructible! They have resisted exposure to carbonization temperatures of 200º C and more. They have survived exposure to 50,000 rems of nuclear radiation, far more than enough to kill any living thing. They have been totally unaffected by any acid. Taken from centrifuge residues, they have been found impossible to cut with a diamond knife; so unbelievably impervious to any such attempts is their hardness.
The eerie implication is that the new minuscule life forms revealed by Naessens's microscope are imperishable. At the death of their hosts, such as ourselves, they return to the earth, where they live on for thousands or millions, perhaps billions, of years!
This conclusion – mind-boggling on the face of it – is not one that sprang full-blown from Naessens's mind alone. A few years ago, I came across a fascinating doctoral dissertation, published as a book, authored by a pharmacist living in France named Marie Nonclercq.
Several years in the writing, Nonclercq's thesis delved into a long-lost chapter in the history of science that has all but been forgotten for more than a century. This chapter concerned a violent controversy between, on the one side, the illustrious Louis Pasteur, whose name, inscribed on the lintels of research institutes all over the world, is known to all schoolchildren, if only because of the pasteurized milk they drink.
On the other side was Pasteur's nineteenth-century contemporary and adversary, Antoine Bèchamp, who first worked in Strasbourg as a professor of physics and toxicology at the Higher School of Pharmacy, later as professor of medical chemistry at the University of Montpellier, and, later still, as professor of biochemistry and dean of the faculty of medicine at the University of Lille, all in France.
While laboring on problems of fermentation, the break-down of complex molecules into organic compounds via a "ferment" – one need only think of the curdling of milk by bacteria – Bèchamp, at his microscope, far more primitive than Naessens's own instrument, seemed to be able to descry a host of tiny bodies in his fermenting solutions. Even before Bèchamp's time, other researchers had observed, but passed off as unexplainable, what they called "scintillating corpuscles" or "molecular granulations." Bèchamp, who was able to ascribe strong enzymatic (catalytic change-causing) reactions to them, was led to coin a new word to describe them: microzymas (tiny ferments).
Among these ferments' many peculiar characteristics was one showing that, whereas they did not exist in chemically pure calcium carbonate made in a laboratory under artificial conditions, they were abundantly present in natural calcium carbonate, commonly known as chalk. For this reason, the latter could, for instance, easily "invert" cane sugar solutions, while the former could not.
With the collaboration of his son, Joseph, and Alfred Estor, a Montpellier physician and surgeon, Bèchamp went on to study microzymas located in the bodies of animals and came to the startling conclusion that the tiny forms were far more basic to life than cells, long considered to be the basic building blocks of all living matter. Bèchamp thought them to be fundamental elements responsible for the activity of cells, tissues, organs, and indeed whole living organisms, from bacteria to whales, and larks to human beings. He even found them present in life-engendering eggs, where they were responsible for the eggs' further development while themselves undergoing significant changes.
So, nearly a century before Gaston Naessens christened his somatid, his countryman, Bèchamp, had come across organisms that, as Naessens immediately recognized, seem to be "cousins," however many times removed, of his own "tiny bodies."
Most incredible to Bèchamp was the fact that, when an event serious enough to affect the whole of an organism occurred, the microzymas within it began working to disintegrate it totally, while at the same time continuing to survive. As proof of such survival, Bèchamp found these microzymas in soil, swamps, chimney soot, street dust, even in air and water. These basic and apparently eternal elements of which we and all our animal relatives are composed survive the remnants of living cells in our bodies that disappear at our death. So seemingly indestructible were the microzymas that Bèchamp could even find them in limestone dating to the Tertiary, the first part of the Cenozoic Era, a period going back sixty million years, during which mammals began to make their appearance on earth.
And it could be that they are older still, far older. Professor Edouard Boureau, a French paleontologist, writes in his book Terre: Mère de la Vie (Earth: Mother of Life), concerning problems of evolution, that he had studied thin sections of rock, over three billion years old, taken from the heart of the Sahara Desert. These sections contained tiny round coccoid forms, which Boureau placed at the base of the whole of the evolutionary chain, a chain that he considers might possibly have developed in one of three alternative ways. What these tiny coccoid forms could possibly be, Boureau does not actually know, but, from long study, he is sure about the fact they were around that long ago.
When I brought the book to Naessens's attention, he told me, ingenuously and forthrightly: "I'd sure like to have a few samples of moon rocks to section and examine at my microscope. Who knows, we might find somatid forms in them, the same traces of primitive life that exist on earth!"
Over years of careful microscopic observation and laboratory experimentation, Naessens went on to discover that if and when the immune system of an animal or human being becomes weakened or destabilized, the normal three-stage cycle of the somatid goes through thirteen more successive growth stages to make up a total of sixteen separate forms, each evolving into the next. (See diagram of the somatid cycle).
All of these forms have been revealed clearly and in detail by motion pictures, and by stop-frame still photography, at Naessens's microscope. Naessens attributes this weakening, as did Bèchamp, to trauma, brought on by a host of reasons, ranging from exposure to various forms of radiation or chemical pollution to accidents, shocks, depressed psychological states, and many more.
By studying the somatid cycle as revealed in the blood of human beings suffering from various degenerative diseases such as rheumatoid arthritis, multiple sclerosis, lupus, cancer, and, most recently, AIDS, Naessens has been able to associate the development of the forms in the sixteen-stage pathological cycle with all of these diseases. A videocassette showing these new microbiological phenomena is available. Among other things, it shows that when blood is washed to remove all somatids external to the bloods red ceils, then heated, somatids latently present in a liquid state within the red blood cells themselves take concrete form and go on to develop into the sixteen-stage cycle. "This," says Naessens, "is what happens when there is immune system disequilibrium." It is not yet known exactly how or why or from what the somatids take shape. Of the some 140 proteins in red blood cells, many may play a role in the process. The appearance of somatids inside red blood cells is thus an enigma as puzzling as the origin of life itself. I once asked Naessens, "If there were no somatids, would there be no life!" "That's what I believe," he replied.
Even more importantly, Naessens has been able to predict the eventual onset of such diseases long before any clinical signs of them have put in an appearance. In other words, he can "prediagnose" them. And he has come to demonstrate that such afflictions have a common functional principle, or basis, and therefore must not be considered as separate, unrelated phenomena as they have for so long been considered in orthodox medical circles.
Having established the somatid cycle in all its fullness, Naessens was able, in a parallel series of brilliant research steps, to develop a treatment for strengthening the immune system. The product he developed is derived from camphor, a natural substance produced by an East Asian tree of the same name. Unlike many medicinals, it is injected into the body, not intramuscularly or intravenously, but intralymphatically – into the lymph system, via a lymph node, or ganglion, in the groin.
In fact, one of the main reasons the medical fraternity holds the whole of Naessens's approach to be bogus is its assertion that intralymphatic injection is impossible! Yet the fact remains that such injection is not only possible, but simple, for most people to accomplish, once they are properly instructed in how to find the node. While most doctors are never taught this technique in medical school, it is so easy that laypeople have been taught to inject, and even to self-inject, the camphor-derived product within a few hours.
The camphor-derived product is named "714-X" – the 7 and the 14 refer to the seventh letter "G" and the fourteenth letter "N" of the alphabet, the first letters of the inventor's first and last names, and the X refers to the twenty-fourth letter of the alphabet, which denotes the year of Naessens's birth, 1924. When skillfully injected, 714-X has, in over seventy-five percent of cases, restabilized, strengthened, or otherwise enhanced the powers of the immune system, which then goes about its normal business of ridding the body of disease.
Let us for a moment return to the work and revelations of Antoine Bèchamp. As already noted, with the fairly primitive microscopic technology available in Bèchamp's day, it was almost incredible that he was seemingly able to make microbiological discoveries closely paralleling, if not completely matching, those of Naessens nearly a hundred years later. We have already alluded to the fact that the microzymas in traumatized animals did not remain passive, as before, but, on the contrary, became highly active and began to destroy the bodies of their hosts, converting themselves to bacteria and other microbes in order to carry out that function.
While the terminology is not exactly one that Gaston Naessens would use today, the principles of trauma and of destruction of the body are shared in common by the two researchers. Had Bèchamp had access to Naessens's microscope, he, too, might have established the somatid cycle in all the detail worked out by Naessens.
So what happened to Bèchamp and his twentieth-century discoveries made in the middle of the nineteenth century? The sad fact is that, because he was modest and retiring – just like Gaston Naessens- his work was overshadowed by that of his rival. All of Pasteur's biographies make clear that he was, above all, a master of the art of self-promotion. But, odd as it seems, the same biographies do not reveal any hint of his battle with Bèchamp, many of whose findings Pasteur, in fact, plagiarized.
Even more significant is that while Bèchamp, as we have seen, championed the idea that the cause of disease lay within the body, Pasteur, by enouncing his famous "germ theory," held that the cause came from without. In those days, little was known about the functioning of the immune system, but what else can explain, for instance, why some people survived the Black Plague of the Middle Ages, while countless others died like flies? And one may add that Royal Raymond Rife's microscope, like that of Naessens, allowed him to state unequivocally that "germs arc not the cause but the result of disease!" Naessens independently adopted this view as a result of his biological detective work. The opposite view, which won the day in Pasteur's time, has dominated medical philosophy for over a century, and what amounted to the creation of a whole new worldview in the life sciences is still regarded as heretical!
Yet the plain fact is that, based on Naessens's medical philosophy as foreshadowed by Bèchamp and Rife, up to the present time, Naessens's treatment has arrested and reversed the progress of disease in over one thousand cases of cancer (many of them considered terminal), as well as in several dozen cases of AIDS, a disease for which the world medical community sadly states that it has as yet no solution what-so-ever. Suffering patients of each sex, and of ages ranging from the teens to beyond the seventies, have been returned to an optimal feeling of well-being and health.
A layperson having no idea of the scope of Naessens's discoveries, or their full meaning and basic implications, might best be introduced to them through Naessens's explanation to a visiting journalist. "You see," began Naessens, "I've been able to establish a life cycle of forms in the blood that add up to no less than a brand new understanding for the very basis of life. What we're talking about is an entirely new biology, one out of which has fortunately sprung practical applications of benefit to sick people, even before all of its many theoretical aspects have been sorted out." At this point, Naessens threw in a statement that would startle any biologist, particularly a geneticist: "The somatids, one can say, are precursors of DNA. Which means that they some-how supply a `missing link' to an understanding of that remarkable molecule that up to now has been considered as an all but irreducible building block in the life process."*
*Intriguing is a recent discovery by Norwegian microbiologists. On 10 August 1989, as Naessens was preparing for trial, the world's most prestigious scientific journal, Nature (United Kingdom), ran an article entitled "High Abundance of Viruses Found in Aquatic Environments." Authored by Ovind Bergh and colleagues at the University of Bergen, it revealed that, for the first time, in natural unpolluted waters, hitherto considered to have extremely low concentrations of viruses, there exist up to 2.5 trillion strange viral particles for each liter of liquid. Measuring less than 0.2 microns, their size equates to the largest of Naessens's somatids. Much too small for any larger marine organism to ingest, the tiny organisms are upsetting existing theories on how pelagic life systems operate.
In light of Gaston Naessens's theory that his somatids are DNA precursors, it is fascinating that the Norwegian researchers believe that the hordes upon hordes of viruses might account for DNA's being inexplicably dissolved in seawater. Another amazing implication of the high viral abundance is that routine viral infection of aquatic bacteria could be explained by a significant exchange of genetic material. As Evelyn B. Sherr, of the University of Georgia's Marine Institute on Sapelo Island, writes in a sidebar article in the same issue of Nature: "Natural genetic engineering experiments may have been occurring in bacterial populations, perhaps for eons." What connection the aqua-viruses may have with Naessens's somatids is a question that may become answerable when Naessens has the opportunity to observe them at his microscope and compare them with the ones he has already found in vegetal saps and mammalian blood.
If somatids were a "missing link" between the living and the nonliving, then what, I wondered aloud in one of my meetings with Françoise Naessens, would be the difference between them and viruses, a long debate about the animate or inanimate nature of which has been going on for years?
To read more, see: The SOMATID - a Pleomorphic, Ultra-microsopic Subcellular Living and Reproducing Entity
How It Works
The theory behind the work of Gaston Naessens is that cancer is caused by a friendly microorganism (present in all cells) that becomes unfriendly. 714X provides nitrogen to the cancer cells, thus causing this microorganism (somatids – “little bodies”) to cease excreting their toxic compounds and the immune system is mobilized. I presume that at that point the immune system kills the cancer cells. “Furthermore, the 714X therapy unclogs the lymph system, which is responsible for removing toxins from the body.”
Gaston Naessens 714X / 714-X
Before talking about 714X, here is an important quote from an article about 714-X or 714X:
People close to Gaston Naessens' work believe that 714-X is best used early. While they believe it may save one in twelve of the terminally ill patients who turn to it on their death beds, and maybe one in six of the advanced cancer patients who try it as a last hope, when it is given early in the disease process, they feel that it might help almost everyone. Further, anecdotally, even in advanced cancer, 714-X may greatly improve quality of life.
While people with advanced cancer, especially those who the orthodox community has given up on and sent home to die, might clamor for a treatment that has a “one in six” chance of survival, I might respond that there are many alternative treatments for cancer that have a much better survival rate for advanced cancer patients than “one in six.” 714X should probably only be used by people who are not yet “advanced.” (See Case Study #1 in my tutorial for more information on what treatments have excellent results for advanced patients.)
Regarding the theory behind this homeopathic medication, Naessens is one of several well-known alternative health researchers who believes a microorganism is involved with cancer. While some consider this microorganism to be a cause of cancer, others simply consider it to be a symptom of cancer. In any case, the attempt to deal with this microorganism leads to the death of the cancer cell.
714X has been heavily persecuted by the governments of both the U.S. and Canada. Gaston was arrested but eventually found innocent. The FDA has issued an “Import Alert” on this substance (as they have for many other top alternative treatment medicines), meaning Americans must go to Canada, and find a licensed doctor who administers 714X (two of my links below happen to be to clinics that I assume use 714X: Dr. Normal Allen, a chiropractor, and the Centre for Integrated Healing in B.C.).
Supercharging This Treatment
Since this treatment must be administered by a doctor in Canada or Mexico, I will leave it to them to supercharge this treatment.
Site – Comments
Source: Gaston Naessens' 714X / 714-X Cancer Treatment
714X
What is 714X ?
Developed by the researcher and biologist Gaston Naessens in the 1970s, 714X is categorized as an immuno-modulator health product aiming to both support a weak immune system or to slow down an over-active one. It intends to restore the body's immune defenses without side effects.
714X is manufactured in Canada by the laboratory CERBE Inc. and has been exported to over 80 countries since 1990.
714X is a colorless liquid. Its therapeutic mode of action requires that it is introduced via injection into the lymphatic circulation (first treatment). In some cases, 714X can be introduced via the respiratory track using a nebulizer (secondary treatment).
The story behind the birth of 714X
Gaston Naessens, a biologist born in France but a Canadian citizen since 1975, is the founding father of 714X. He has been working in hematology since 1945 when he finished his studies specialized in Physics, Chemistry and Biology (PCB). For over 66 years, this researcher, who discovered the SOMATID and its cycle in the 1950s, continues to study the role played by this particle in the maintenance of our natural defenses including the immune functions. The somatid, which according to him, is the smallest unit of life, was discovered in fresh blood after numerous and repeated systematic tests where he could establish its evolutionary forms in a 16 phase pleomorphic cycle.
Here is a diagram of the Somatidian cycle as observed under a microscope by Gaston Naessens:
The discovery of the somatid and knowing the existence of its life cycle would have been sufficient to satisfy the intellectual curiosity of a researcher working in fundamental research. However, for Gaston Naessens, there was a step further to take. Knowing that a microscopic observation of blood could reveal the state of one’s immune defenses was not sufficient. Knowing that the disease was inevitable and nothing was done to prevent it did not correspond to his code of ethics. This extra step was thus the search for natural ways that could restore the functions of our defense system without causing any harm to all the blood’s elements. This work, which began in the 1950s, continues today and is embodied in the design of many health products intended to act on the Somatidian cycle . It was in the 1970s, following several experiences with other health products he had made available to the European public in the 1950s and 1960s, that he created a new product: 714 X . (non-toxicity confirmed in 1978).
714X is a non-toxic natural health product capable of restoring the biological terrain when the immune defense function is too weak or too active.
Despite the obstacles and resistance to his new ideas, Gaston Naessens continues to move forward, and his perseverance has earned him at least the satisfaction of collaborating, as an independent researcher, towards the emergence of a new paradigm in health and to offer humanity effective and non toxic health products.
How does this product work ?
714X works in two ways:
Thus, the inflammatory process, common to many degenerative diseases, fades and comes back to its normal state. Cell, tissue and organ repairprogress at a rate specific to each individual.
How to administer 714X ?
Usage protocol
714X is a unique product due to its mode of intromission. In addition to this, 714X normalizes the biological terrain using the lymphatic circulation as a gateway into the body.
The particular choice for the mode of intromission of the product is based on the belief of its designer, who is convinced that the lymphatic system is the main highway system, one that facilitates the elimination of metabolic toxins circulating in the blood and that brings to the cells essential elements for their optimal functioning.
Choosing the lymphatic circulation as a mode of entry has practical unavoidable consequences as it becomes necessary to deal with anatomic realities. Nature has endowed the human body with a double lymphatic circulation. A large and a small circulation, each with their drainage area, that flow into the bloodstream.
Lymphatic circulations' drainage zones
To access the large lymphatic circulation which drains 75% of the body surface, the mode of intromission is the perinodularl injection (around the lymph nodes) in the right inguinal region (the groin).
Basic treatment with 714X requires a box containing two vials of 6.5 ml of product. This quantity allows 21 days of injections to constitute a cycle.
To access the small lymphatic circulation, the preferred method is the introduction of the product by inhalation with the use of an ultrasonic nebulizer that allows the absorption of the product via the small glands that line the respiratory tract (714X divided into particles smaller than 5 microns).
714X's secondary treatment (the nebuliser method) must be performed in addition to the perinodular injection. It requires 3 boxes of 7 ampoules of 2 ml for 21 days of treatment which constitute 1 cycle.
The perinodular injection
Self-injection, even when one has already decided to use 714X is an unfamiliar process. The word injection itself raises some apprehension.
At the beginning of the treatment, it is completely understandable to be hesitant and to worry about self-injecting in the right area.
The location of the injection site is the first and most critical step.
714X users’ feedback allow us to say that the injection technique, when properly mastered the first 5 days, can be considered an enjoyable daily activity which can be incorporated in your daily schedule as a relaxing time. This activity then becomes a simple daily gesture which can be paired with listening to pleasant music in a relaxing and comfortable setting.
Finding the injection site
For children weighing less than 30 kg (66 pounds), the injection site is located on this imaginary line, 1 to 2.5 cms (0.5 to 1 inch) above the femoral artery pulse.
By putting pressure on the femoral artery where the pulse is felt, the three deep lymph nodes are brought up to the surface. The product injected into the periphery of these deep lymph nodes will be absorbed by one of these nodes, hence the term: perinodular injection. The optimal injection zone has a surface area comparable to a small disc measuring 2 cm. Day after day, the needle does not have to be inserted in exactly the same spot, but in the same area, leaving some room for maneuver.
Two important points to remember concerning finding the injection site:
Please refer to the 5_steps_perinodular_injection.pdf for the five steps of the perinodular injection.
Compatibility of 714x with other treatments
714X is a health product which is introduced into the lymphatic circulation. This is one of the characteristics that makes 714X unique.
Consequently, this product never comes in contact with ingested food or any part of the digestive system. 714X has no direct interference with food, natural health products or prescribed medications.
714X is considered as a product of Universal Health totally compatible with pharmacological products as well as natural health products, because it is through the lymph that 714X flows into the bloodstream to act on white blood cells (leukocytes), and on the cellular environment. 714X acts on the biological terrain.
In part due to its specific action on white blood cells’ (leukocytes) cytokine receptors, 714X not only acts on immune defense but it also supports the expected positive effects of other healthcare products taken orally. 714X works with all other products introduced externally.
In the event that a patient must temporarily receive certain conventional treatments or a surgical intervention, 714X taken simultaneously can be beneficial as it acts as reinforcement to invalidate their unavoidable side effects by supporting the vital energy and the natural defenses.
714X is not only universally compatible with all products, but it offers as well the benefit of invalidating the adverse side effects of other products, while supporting the vital energy.
In oncology, and considering that cancer is a huge public health concern, 714X becomes a helpful support to go through the intense periods of targeted treatments (surgery, chemotherapy, radiation, etc..), as well as during recovery periods and therapeutic breaks.
Since it is non-toxic, 714X can be used preventively in healthy people. Immune resistance is further increased to accommodate the many challenges of personal and / or professional life.
With non conventional treatments
Because it supports the body's natural defenses, 714X can be taken simultaneously with most natural health products.
The only exception to this statement remains anti-angiogenic products of natural or synthetic source (eg, shark or bovine cartilage).
This is not to say that these products are not effective, but their mode of action is not complementary with 714X.
The reason for this incompatibility is as follows:
The effect of anti-angiogenic products of any kind (used for cancer treatment in the model which focuses on the elimination of the tumor) is to create oxygen deprivation by cutting the blood flow that feeds the tumor. The intended effect is to reduce the growth of the tumor by depriving it of nutrients.
714X needs to go through the blood circulation near the tumor so that the tumor necrosis factor secreted by the reactivated white blood cells can act on the tumor and reduce it.
The secretion of the tumor necrosis factor is the white blood cells defense mode of activity by which all of their secretions, released into the blood, react and shrink the tumor, regardless of its location in the body.
With certain conventional treatments
This section has dealt with how 714X is compatible with different health products that go through the digestive system.
In the case of therapeutic approaches in particular medical interventions (as for the case of cancer for example) 714X can be taken simultaneously with conventional care. As it acts on the natural defenses of immunity, 714X is complementary to conventional treatments and will not counteract them. On the contrary, 714X can reduce, and even eliminate much of the undesirable side effects usually associated with conventional treatments, thus permitting a better quality of life.
Moreover, as 714X acts on the lymphatic circulation, taking a cycle of 714X before surgery will minimize the risk of uncontrolled spread of anarchical cells elsewhere in the body as these can be drawn into the lymphatic system (not only in the case of cancer).
714X taken before surgery will provide better cell, tissue and organ repair after surgery (wound healing).
Statistics and data use
In everyday language, the notion of "statistics" in health often involves the estimated success rate of a specific product against a particular pathology.
For 714X, we are often asked the following question: "Do you have statistics on your cancer product? "This approach is very legitimate from the point of view of the consumers who are accustomed to medication that acts on the disease.
This expectation of the consumer, regarding the effectiveness of the product 714X against his own illness, is based on the conventional approach. This is the usual way of doing things in conventional medicine and it is always an external product that comes in to correct the symptoms of the disease.
In natural medicine, a product acts upon the biological terrain. This is a different view. In the biomedical model, the predictive ability of the effects of a chemical product is made possible because the product has been studied and measured in a laboratory (often on mice), based on the toxicity of the molecule. The final product is designed to achieve measurable benefits that will outweigh the inevitable incurred risks.
It is different for 714X as it is non-toxic. In the holistic model of health, also known as global health model, all the elements of the context of one’s life are very important. Since the natural products that are offered are non-toxic, they aim to improve natural health factors in order to support the biological terrain, rather than acting locally to neutralize symptoms of a local physiological disorder
This is why within this global health model to which 714X pertains to due to its non-toxic nature, it becomes impossible to make mathematical predictions on the absolute effectiveness of the product, because it is the uniqueness of each one of us that will determine the speed and extent of efficacy of the product in its context.
In short, for 714X, as for any natural health products (eg vitamin C) or special treatments (eg massage), the ultimate impact will always depend on the biological terrain unique to each individual and life context in which each person evolves.
The perception of the impact of 714X, as a health treatment, is usually shown through individual observations felt and manifests through quality of life criteria such as one’s vitality, sleep, appetite, etc.
Although it acts in all cases on the lymph and the white blood cells (leukocytes), it is not possible to attribute a predictive character to 714X because it integrates itself to the biological terrain of each individual, with their own uniqueness. The physiologic effects are measureable little by little as the cleansing and body repair progress, according to each individual biological terrain.
Clinical experience from the last thirty years (22 years of use under the authority of a governmental regulatory agency) means that 714X is a product that has surpassed the « test of time ». We can say with complete confidence that its utilization brings after the first 21 days of use a better quality of life. This is expressed in many ways according to each individual and depending on the evolution of the disease, the care that was given and each person's experiences.
In general, the effects of 714X under the parameters of conventional blood tests are usually measurable after a minimum of 3 cycles of use.
Scientific data on 714X
714X is the invented name of Triméthylaminohydroxybicycloheptane chloride.
Chemical formula
Chemical composition
714X is an isotonic solution at physiological pH (7) containing nitrogen as the main active ingredient, camphor as a vehicle, or a nitrogenated derivative of camphor, at a level of 0.09 mg/ml (complying with the pharmaceutical industry’s norms of injectable solutions), mineral salts, and 18 different trace elements (metallic elements), measured in parts per million, and magnesium at a level of 6.5 ppm. these trace elements, even in trace amounts, do have a biological significance.
The level of sodium chloride (NaCl) is estimated at 8.2g/litre.
A plasma emission spectrometry study identifies the 18 following elements measured by the following parts per million):
Aluminum < 0.5 ppm Calcium 0.5 ppm Mercury < 1.0 ppm
Antimoine < 1.0 ppm Chrome < 0.1 ppm Molybdenum < 1.0 ppm
Arsenic < 1.0 ppm Cobalt < 1.0 ppm Nickel < 0.1 ppm
Baryum 0.7 ppm Cuivre 0.01 ppm Phosphore < 5.0 ppm
Bore < 0.05 ppm Fer < 0.1 ppm Plomb < 1.0 ppm
Cadmium < 0.05 ppm Magnésium 6.5 ppm Zinc 2.0 ppm
Conclusion
The absence of proteins and immunoglobulins shows that this is not an immune serum prepared after injection to animals. 714X is not a vaccine. There is no risk of allergies or anaphylactic shock.
The presence of sodium chloride at a level of 8.2 g / liter shows that this is an isotonic solution with a pH of 7 (physiological solution). This solution complies with norms for injectable solutions of the pharmaceutical industry.
A mass spectrometry coupled with a chromatography reveals the presence of camphor or trimethyl-1.7.7 bicyclo (2.2.1.) heptanone-2 whose concentration we measured as 0.09 mg / ml (90 ppm). A nitrogenated compound and hydrochloric acid were also identified.
The comparative study using camphoroxime shows that this molecule does not exist as such in the analyzed sample of 714X. The precise nature of the nitrogenated compound contained in 714X could not be clearly identified.
Eighteen metals (metallic elements) were measured. They were all found at trace levels (parts per million) and considered to be of no biological significance, except for magnesium which at 6.5 ppm was too low to be given a therapeutic property. (This is the opinion of the private laboratory. However, the manufacturer claims that these trace elements, even in trace amounts, do have a biological significance)
Summary of the chemical analysis
Ultimately, 714X is an isotonic solution at physiological pH (7) containing camphor or a nitrogenated derivative of camphor, at a level of 0.09 mg/ml, complying with the pharmaceutical industry’s norms of injectable solutions.
Therapeutic class
714X belongs to a health products category that acts upon natural defenses including the immune function.
Depending on the circumstances, 714X acts on a severely weakened immune system (by strengthening it) or on an overactive immune system (by slowing it down). For this reason, 714X is recognized as an immuno modulator.
Moreover, to date, 3 patents confirm that 714X is an immunomodulator.
Canadian Patent: 2010.CA02297998
European Patent: 2005.EP1251841-B1
American Patent: 2003-6-596-295
Research Report – Immunologic test applied to 714X
(vitro Effects of 714X on mononuclear cells of peripheral blood)
Sponsor:
Diane Van Alstyne, Ph.D.
Inventors Ink
#23-130 MacPherson Ave.
Toronto, Ontario, CANADA M5R 1W8
Period of Experimentation:
March 1999, Boston, Massachusetts, USA
Results and conclusions
Peripheral blood mononuclear cells and monocytes exposed to 714X in vitro show the following effects:
Based on the foregoing data, the sponsor suggests that 714X contains at least one component which acts as a substance that promotes the induction of cytokine in vitro and has the following characteristics:
TNF-α, IL-1β, IL-6 and IL-8). These data provide scientific evidence to 714X’s immunomodulatory role.
It is believed that the 714X enhances the immune response and plays a role in the removal of the tumor cell. The results appear to support this theory by suggesting that induction of proinflammatory cytokines represent at least one mechanism responsible for anti-tumor activity in vivo of 714X.
Assurance of Quality Control:
Data reviewed and report provided by researcher Diane Van Alstyne, Ph.D.
Report published 25 August 2000
To read more, see: 714X | Cerbe Distribution Inc
Manufacturing
https://www.cerbe.com/sites/default/files/videos/production_en.mp4 (video showing the manufacturing process of the 714X product.)
The complete manufacturing process is comprised of four steps:
At each of these steps, the strictest aseptic norms and standards are adhered to, ensuring the product is safe and secure. CERBE, the manufacturer, guarantees the sterility of its products as all of its manufactured products are sterilized after bottling using traditional autoclave sterilization procedures.
CERBE voluntarily adheres to good manufacturing practice (GMP)
Once these four steps are complete, CERBE Inc. can assure its clients and consumers of the delivery of a natural health product that is sterile, safe and ready to use in Canada in collaboration with the Special Access Program of Health Canada or for exportation abroad.
The manufacturing process
The bottling process
The sterilization process
Labelling
The manufacturing process
The mix of unique base products The products of CERBE Inc. are innovative products, unique and specifically developed to act on the immune system without negative side effects. The first step is therefore the mix of its base products following a new and unique process of arranging molecules. The innovative nature of Gaston Naessens’ manufacturing process is confirmed by the attainment of the following patents:
U.S. Patent 2003
European Patent 2005
Canadian patent 2010
The bottling process
This step is performed in a sterile lab, in an enclosed space especially built and designed for this stage of the manufacturing process, with ultra-specialized and modern equipment specifically designed for the manufacturing needs of CERBE Inc. The best practices of the laboratory are applied in order to maintain the highest quality standards in manufacturing in the natural health products industry.
The sterilization process
This step is crucial to ensure the safety of products, injectable or otherwise. All of the products manufactured by CERBE Inc. are mandatorily sterilized using traditional autoclave sterilization procedures. This means that all products are sterilized at 212 degrees centigrade under 18 lbs of pressure for a minimum period of 20 minutes. This self-imposed requirement of CERBE Inc. necessitates the use of specialized bottles able to support extreme high temperatures. None of CERBE Inc.’s products are bottled in plastic containers.
Labelling
Once the bottling and sterilization processes are completed, the labeling is done in a completely different laboratory specially designed for this step. Once again, a final quality assurance check is done, one bottle at a time, under ultra-violet lighting, before finally placing specific regulatory standard labels for each of the products. For each product, the identification number, expiration date, and the specification of bottles for exportation are clearly marked on each commercial label.
Source with video embedded: Manufacturing | Cerbe Distribution Inc
Gaston Naessens & The Somatid
September 9, 2016
Gaston Naessens was treated badly by the world for creating his ingenious invention he called a Somatoscope. Today, these devices are called phase contrasting microscopes that do live cell blood exams. The medical mafia has been doing its best to keep practitioners, who use these incredible devices, out of the free market; because of what they reveal that can get a patient well. However, as the battle rages on in the free market place, more and more the western medical system is failing to keep these devices from emerging. In truth, every western doctor on the planet should be using these incredible microscopes to help get their patients well. Look below and learn more!
Still alive at age 92, Gaston Naessens was born March 16, 1924, in Roubaix, in northern France, near the provincial capital of Lille, the youngest child of a banker who died when his son was only eleven years old. In very early childhood, Gaston was already showing precocity as an inventor. At the age of five, he built a little moving automobile-type vehicle out of a “Mechano” set and powered it with a spring from an old alarm clock.
Continuing to exhibit unusual manual dexterity, a few years later Gaston constructed his own home-built motorcycle, then went on to fashion a mini-airplane; large enough to carry him aloft. It never flew, for his mother worried he would come to grief, and secretly burned it on the eve of its destined takeoff.
After graduation from the College Universitaire de Marcen Baroeul, a leading prep school, Gaston began an intensive course in physics, chemistry and biology at University of Lille. When France was attacked and occupied by Nazi forces during Word War II, young Gaston, together with other fellow students was evacuated to southern France. In exile near Nice, he had the highly unusual opportunity to receive the equivalent of a full university education at the hands of professors also displaced from Lille.
By the war’s end, Naessens had been awarded a rare diploma from the Union Nationale Scientifique Francaise, the quasi-offical institution under whose roof the displaced students pursued their intensive curriculum. Unfortunately, in an oversight that has cost him dearly over the years, Naessens did not bother to seek an “equivalence” from the new republican government set up by General Charles de Gaulle. He thus, ever since, has been accused of never having received an academic diploma of any kind.
Inspired by his teachers, and of singular innovative bent, Gaston, eschewing further formal education– “bagage universitaire” (academic baggage) as he calls it — set forth on his own to develop his microscope and begig his research into the nature of disease. In this determination, he was blessed by having what in French is called jeunesse dorfee, or gilded childhood — “born with a silver spoon in his mouth,” as the English equivalent has it. His mother afforded him all that was needed to equip his own postwar laboratory at the parental home.
— Taken from the book titled “Suppressed Inventions” written by Johnathan Eisen (Page 157 of 560)
What now follows are two videos that reveal Gaston Naessens Somatoscope, how it works and how it was instrumental in revealing the 16 stage cycle of the somatid ability to pleomorphosize.
Source: Gaston Naessens & The Somatid - KFFMenterprises
Gaston Naessens and 714X
By Dr. Gaston Naessens and Jacinte Levesque Naessens
Image courtesy of Cerbe Distribution, Inc.
A diagram of the Somatidian cycle as observed under a microscope by Gaston Naessens.
Gaston Naessens, a French-born researcher based in Sherbrooke, Québec, who has been at work since the early 50s, is a true pioneer in the field of live blood observations.
Through the optical performance of his unique light microscope (the somatoscope), Gaston Naessens discovered the smallest unit of life: the somatid.
He was able to understand the life cycle of the somatids through their different evolutive forms. This led him to a further observation of an “inner biological protection gate” that reveals the state of the immune system.
This inner protective gate, also a witness of the natural defenses, can be altered by a combination of external and/or internal factor. If the “inner gate” is being over-challenged, it breaks down the homoeostasis of blood that can thereafter lead to various types of degenerative disorders (including cancer), initiating with inflammation, the common precursor of all degenerative diseases.
Naessens was able to monitor the state of the immune system from an innovative perspective: the visual observation of live blood through his specific assessment of the somatidian cycle.
Immunotherapy, the fourth arm of cancerology (after surgery, chemotherapy and radiology), was declared a major scientific breakthrough in 2014. Naessens’ vision of cancer linked to the immune system is thus proving to be a sound innovative way to address disease from an epigenetic perspective.
As early as 1961, Naessens proposed a therapeutic agent / therapy capable of addressing the immune system as it was in its evolution with cancer. This was then considered heretic. Today, it fits perfectly with the scientific revolution that encompasses wider factors rather than the strict genetic components of degenerative diseases.
Naessens’ knowledge and understanding of the somatidian cycle as a witness of the evolution of the disease, allowed him to create a restorative product for the immune system. 714X is a nontoxic health product capable of restoring the normality of the somatidian cycle, consequently restoring the inner balance.
714X has been granted four patents testifying of its uniqueness, confirmed by various juridictions. (Patents obtained: 2003 USA, 2005 EC, 2010 Canada, 2014 Japan.)
It is important to recall that 714X, a proprietary blend, is a true immune modulator that can be either used for curative purposes, alone or in combination with conventional modalities, or simply used alone as a preventative agent.
Naessens’ vision of health is highly compatible with the holistic approach where many factors impact the biological system including the emotional, the intellectual and the spiritual factors. It is thus essential to address each person as the unique expression of a biological signature.
A trustful partnership between consumers and their health care providers (conventional and/or alternative) is the new trend that Naessens supports entirely, bringing integrative medicine to the forefront of a new era.
Gaston Naessens, at 92 years old, is still young at heart and continues to work at his own pace, in peace, always eager to find nontoxic solutions to maintain optimal health.
For more information on Naessens work or on the 714X product visit the Cerbe Distribution, Inc. web site.
See also Change of Strategy in Cancer Care Management: Cancer Immunotherapy a Major Breakthrough Leading to a Paradigm Shift by Dr. Gaston Naessens and Jacinte Levesque Naessens, originally published in Wise Journal, Fall 2015.
Source: Gaston Naessens and 714X | Foundation for Alternative and Integrative Medicine
The Amazing Wonders of
Gaston Naessens
February - March 1994
The landscape of medical science is on the verge of being radically altered forever by the use of a powerful microscope (the Somatoscope) developed by Gaston Naessens of Quebec, Canada, This incredible device reaches magnification levels of 20,000 to 30,000 diameters—well above the 2,500 diameter limit of conventional microscopes. The sheer magnitude of the difference in performance gives the appearance of either a gross violation of the laws of physics, or fraud.
Its radical departure in performance from optical and scanning electron microscopes registers this as a truly great discovery. Unfortunately, in most fields of science, a great deal of effort is put forth into listing why something will not work instead of attempting to duplicate the results. This in turn creates a situation where what was science, turns into religion where the orthodox dogma is to be taken on faith, and that which defies dogma is to be persecuted as heresy.
Establishment of a dogma slows down the rate new discoveries can be made. In the medical fields, slow acceptance of new ideas can cause many needless deaths. This is the case with the supermicroscope and the discoveries of B&hamp, Rife and Naessens.
Read more at: The Amazing Wonders of Gaston Naessens by Steven R. Elswick
Dr. Gaston Naessens
Gaston Naessens, ND.
Gaston Naessens, ND is the president, founder, and CEO of Cerbe Distribution, Inc., a private laboratory in Québec, Canada specializing in fundamental research in biology, including hematology.
Cerbe is also the manufacturer of Triméthylaminohydroxybicycloheptane chloride (714X) for which four patents have been granted [2003 (USA), 2005 (Europe), 2010 (Canada) and 2014 (Japan)].
He is a biologist researcher engineer and developed a revolutionary microscope, called the somatoscope, capable of observing unstained living matter. The somatoscope enabled him to discover a new particle in human blood, he calls the somatid. From this, he developed the Somatidian theory and developed new responses to diseases affecting the immune system.
Source: Dr. Gaston Naessens | Foundation for Alternative and Integrative Medicine
Source websites:
Cerbe Distribution Inc | A Trustworthy Partner for Better Health
Gaston Naessens & 714X
Dr. Gaston Naessens | Foundation for Alternative and Integrative Medicine
Gaston Naessens and Somatid biology
Book on Gaston Naessens: The Persecution and Trial of Gaston Naessens by Christopher Bird
Gaston Naessens and Somatid biology
The landscape of medical science is on the verge of being radically altered forever by the use of a powerful microscope (the Somatoscope) developed by Gaston Naessens of Quebec, Canada. This incredible device reaches magnification levels of 20,000 to 30,000 diameters — well above the 2,500 diameter limit of conventional microscopes. The sheer magnitude of the difference in performance gives the appearance of either a gross violation of the laws of physics, or fraud.
Its radical departure in performance from optical and scanning electron microscopes registers this as a truly great discovery. Unfortunately, in most fields of science, a great deal of effort is put forth into listing why something will not work instead of attempting to duplicate the results. This in turn creates a situation where what was science turns into religion where the orthodox dogma is to be taken on faith, and that which defies dogma is to be persecute as heresy.
Establishment of a dogma slows down the rate at which new discoveries can be made. In the medical fields, slow acceptance of new ideas can cause many needless deaths. This is the case with the super-microscope and the discoveries of Bechamp, Rife, and Naessens.
HISTORICAL NOTES
In the 1930s, an obscure and dedicated scientist, Royal Raymond Rife, had successfully developed the Universal Microscope which was able to provide amplification levels of 60,000 times without killing the specimens! Rife was able to observe live viruses and their reaction to certain stimuli. His observation that bacteria could change into viruses and viruses could change form violated the strongest medical dogma — the germ theory of disease.
By 1934, after learning how to seek out and destroy the insidious cancer virus, Rife opened a clinic in which he cured 16 out of 16 patients within 3 months! Working side by side with some of the most respected researchers in America, Rife treated patients electronically to kill the virus and then allowed the body's immune system to restore the body to full health. Many prestigious ( and competent ) organizations and institutions oversaw and verified much of Rife's work during the 1930s.
Independent physicians using Rife's therapy were treating and curing as many as 40 patients per day. Other degenerative conditions and illnesses such as cataracts, herpes and tuberculosis were found to be reversible and curable with Rife's equipment. This work was described in various medical journals of the time as well as the Smithsonian Institution's annual report and Science Magazine. Unfortunately, Rife's success attracted the attention and wrath of the American Medical Association (AMA) and the powerful pharmaceutical companies - the organised opposition of the medical fields.
Although Rife's work was in direct conflict with the orthodox views of his time, he was supported by many top-rated doctors. Many of these doctors continued using these devices in secret in defiance of the AMA and the US government. The carefully documented records kept by these brave doctors and testimonials by their patients vindicate Rife's theories. Many of these case histories and anecdotes about Rife's treatment can be found in the book "The Cancer Cure That Worked" by Barry Lynes.
The fascinating work of Rife was suppressed and he — like Nikola Tesla before him — joined the ranks of the forgotten inventors of the early part of this century. It has only been in the past few years that the general public has begun to develop an awareness that there is something wrong in the technical world.
THE MODERN UNIVERSAL MICROSCOPE
What Rife accomplished optically in the 1930s with his Universal Microscope, Gaston Naessens accomplished with a combination of optics and electronics in the 1940s in his Somatoscope. Born on 16 March 1924 in Roubaix, France, Gaston displayed a predisposition to be an inventor when at the age of five he built a little moving auto-like toy from a Meccano set and powered it with an alarm clock spring. Later, he built a home-made motorcycle and a mini-airplane!
While attending the University of Lille, Gaston nearly had his education disrupted by the German invasion. Fortunately, Gaston and his fellow students escaped to Nice where they carried on their education in exile. He was awarded a diploma from the Union Nationale Scientifique Francaise — a quasi-official institution under whose auspices the education of the displaced students continued. He did not bother seeking an equivalency degree from the de Gaulle government when French rule was restored.
At the young age of twenty-one, frustrated by the limitations of conventional microscopes, Gaston set out to build a superior microscope. Technical assistance was provided by German craftsmen from Wetzlar, Germany, who checked out many of Gaston's ideas on optics. Privately, Gaston devised the electrical manipulation of the light source. Once the technical aspects were resolved, Gaston had the body of his microscope constructed by Barbier-Bernard et Turenne, technical specialists and defence contractors near Paris.
THEORY OF OPERATION
The Somatoscope mixes light from two orthogonal light sources — a mercury lamp and a halogen lamp. The light from both sources enters a glass tube at 90 degrees from each other. As the light waves beat against each other, a strong carrier wave of light emerges and travels down the light tube. ( It should be noted that two electromagnetic fields superimposed on each other at 90 degrees is a classic scalar formation! ) As the light travels down the tube, it passes through a monochromatic filter which forms it into a monochromatic ray. The ray is then passed through a large coil that surrounds the tube. The coil's magnetic field divides the ray into numerous parallel rays that are then passed through a Kerr cell which increases the frequency of the ray before being injected onto the specimen.
The light, which contains the carrier and a mixture of selected signals in the UV range, stimulates the biological material in the Somatoscope to the point that the specimens give off their own light. (Rife referred to this as luminescence.) This is the key to the ultra-high resolution that has been achieved by Gaston Naessens.
Conventional microscopes pass light through the specimen which theoretically limits the resolution of optical microscopes to the wavelength of light. The finest optical microscopes have achieved magnification levels of 2,500 diameters. At levels above this, the resolution is limited by the wavelength of light and further magnification merely creates a blur! Higher resolutions have been achieved by microscopes that do not use lenses, but instead use apertures which are smaller than the wavelength of light. One such microscope engineered at Cornell University has achieved a resolution of 400 angstroms — a far cry from the 150 angstroms achieved by Naessen's Somatoscope.
The Somatoscope does not attempt to illuminate the specimen by passing light through two small objects. Instead, the illumination source is actually stimulating the specimen to the point where it generates its own light. The light itself expands as it moves outward and because the specimen itself is generating the light, the physical restrictions encountered by regular optical microscopes no longer apply. By converting the specimen into a light source, Gaston Naessens has converted the magnification problem from one of resolution to that of light detection! At magnification levels above 5,000 diameters, light levels drop off to the point that film is necessary, but the resolution is there.
To further research along the lines he has pioneered, Gaston has developed junior models of his Somatoscope for field use. These field units allow researchers to obtain illumination and stimulation of the specimens of the larger unit. The field units are capable of magnifying 6,000 – 7,000 diameters, although routine work will usually be at 3,500 – 4,000 diameters. The lower light levels of the higher magnification requires that a lower level of magnification be accepted for field use in order to maintain portability in the smaller units. One such unit will be in use in Colorado Springs at Clifford and Associates.
The Somatoscope has enabled researchers to discover the importance of colour and its relationship to the material being observed. The wavelengths of light generated are related to the size of the object and the health of the cell. For instance, the red blood cells vary from yellow/green to orange (540 nm to 580 nm) and white blood cells are rich in blue/violet (490 nm to 510 nm). Exposure to toxic materials, even in minute amounts, causes significant shifts in colour. Even 'safe' amounts of toxic materials like mercury and the aluminium in toothpaste cause significant degradation to red blood cells as I was able to witness from specimens on a videotape produced from the Somatoscope.
THE SOMATID CYCLE
In a long lost chapter in the history of science, a violent controversy took place in France between the illustrious Louis Pasteur and Antoine Bechamp, a noted professor of physics, toxicology, medical chemistry, and biochemistry. Bechamp's work led him to discover "microzymas" (tiny ferments), which were characterised by a host of small bodies in his fermenting solutions.
After years of study, Bechamp came to the conclusion that these microzymas were more basic to life than cells. Even with his crude equipment, he was able to observe that the microzymas underwent dramatic transformations during their life cycle. This caused Bechamp to champion the idea that the cause for disease lay within the body. Pasteur's germ theory held that the cause came from without. Pasteur's outspokenness helped the germ theory win out and it has dominated medical thinking for the past century.
Now, a hundred years later, Gaston Naessens has discovered an ultra-microscopic, subcellular, living and reproducing microscopic form which he christened a "somatid" (tiny body). This new particle could be cultured outside the bodies of the host. Naessens also observed that the particle had a pleomorphic (form-changing) life cycle, which has sixteen stages. Only the first three stages of the somatid's life cycle are normal.
Naessens discovered that when the immune system is weakened or disrupted, the somatids go through the other thirteen stages. The weakening of the immune system could be brought about by a number of causes, such as exposure to chemical pollution, ionising radiation, electric fields, poor nutrition, accidents, shock, depression, and many more.
Incredibly, Naessens' research has resulted in the association of degenerative diseases (rheumatoid arthritis. multiple sclerosis, lupus, cancer and Aids) with the development of various forms in the sixteen-stage pathological cycle. The ability to associate the disease with specific stages has enabled Naessens to 'prediagnose' conditions in advance of when they would clinically appear.
This discovery puts Gaston Naessens at odds with the orthodox medical philosophy of today which has embraced Pasteur's germ theory wholeheartedly. Naessen's work is repeatable. The ability to culture somatids is a bell-wether to the rewriting of micro-biology!
Naessens has stated:
"I've been able to establish a life cycle of forms in the blood that add up to no less than a brand new understanding of the basis of life. What we're talking about is an entirely new biology, one out of which has fortunately sprung practical applications of benefit to sick people, even before all of its many theoretical aspects have been sorted out."
714X
The research of Gaston Naessens has culminated in the discovery of 714X — an enzyme which helps the immune system do its job. 714X is a derivative of camphor and is injected interlymphatically — a process that the medical fraternity holds to be impossible. Yet the fact remains that many people have learned how to administer the medication through the lymph nodes.
When properly administered, 714X stabilises and strengthens the immune system in most cases. This allows the immune system to go about its normal business in ridding the body of disease. In other words, cancer is treated like an infection, not a state of cells.
Like Bechamp and Rife before him, Gaston states unequivocally that "germs are not the cause, but the result, of disease."
714X will not help everyone — especially where there has already been extensive use of chemotherapy and radiation. Chemotherapy and radiotherapy wipe out the immune system and other bodily resources.
THE SECOND CHANCE
The cancer death toll between 1970 and 1986 ( in the U.S.? ) was approximately 6 million. Sadly, the conventional treatments of chemotherapy and radiation are nothing more than slow death sentences that enrich the cancer industry. Possible miracle cures are quickly quashed by the FDA (Food and Drug Administration) and the various medical societies around the world. It is a sad commentary that in a country that prides itself on freedom, terminally ill patients cannot make an informed decision to participate in experimental treatments that may save their lives.
714X is available in the United States. "Writers and Research" is one organisation working closely with the FDA and the IRN ( Institution Review Board ) to do work with 714X legally and ethically. 714X is an injected medication and must be prescribed by a doctor.
For a list of doctors prescribing 714X or an information packet, contact:
WRITERS AND RESEARCH
4810 St Paul Boulevard
Rochester, NY 14617 USA
Phone: 1–800–448–4332
Source: Gaston Naessens and Somatid biology
The Story of Gaston Naessens Featured in Canada’s Saturday Night Magazine
In it’s December issue, Canada’s popular magazine, Saturday Night, featured the trials and victories of eminent biologist Gaston Naessens. The well-written 12 page article chronicled the life of Naessens from the discovery of the somatid cycle (see Figure 1) to the development of the formula 714-X, to the trials and persecution he faced and continues to face. Below is a historical summation of the article:
Late 1940’s – From the work of individuals such as Béchamp and Emile Doyen, Naessens began work on what would become the somatoscope. What would later be termed dark-field microscopy (but not as sophisticated), Naessens’ instrument allowed him to examine live blood at extreme magnifications as well as with exceptionally high resolution. One improvement with this instrument is its ability to see particle via light refraction as opposed to traditional staining methods.
Mid 1950’s — Moved lab to Paris from Lyon, France. Opposition began to mount from the traditional medical authorities due to innovative theories and treatments, not to mention successes.
Early 1960’s — Naessens treated over 10,000 individuals afflicted with various illnesses, many life-threatening, with extraordinary results. On the other side, he was twice brought before the “bar” (medical authorities). He was fined heavily and forced to close his Paris lab. Much of his equipment was confiscated.
1962 — Naessens tried again to start his laboratory on the island of Corsica, but Corsica was still France. Patients continued to seek him out, as did the authorities.
1964 — Naessens pursued his work in Canada, leaving Corsica with only a few key components of his microscope.
Late 1960’s — He received a $25K grant from the National Research Council as a consultant on microscopy. However, this was quickly revoked due to his troubles with the French medical authorities of past years.
1971 — Gaston Naessens began again as a medical researcher. The head of the MacDonald Stewart Foundation (organization which funded orthodox cancer research for many years), David Stewart, agreed to finance Naessens’ research personally and establish a laboratory for him on the MacDonald Tobacco Company’s premises in Montreal. This infuriated the orthodox oncologist on the research wing, and Naessens was forced to move to a low-key spot in Rock Forest on the banks of the Magog River near Sherbrooke, Canada.
1972 — Initial meeting regarding additional funding for research relating to Naessen’s somatid theory and the formula 714-X went well. An assistant professor of pathology, Daniel Perey, volunteered to head the proposed investigation.
Perey visited Naessens laboratory and described it as nothing short of a revelation. However, his excitement was not shared by all. Co-investigators with Perey questioned the validity of the somatid cycle, as this contradicted the definition of disease taught in medical schools.
Late 1972 — Perey extolled Naessens’ contributions to the field stating, “The scope and insight which Mr. Naessens has brought to this area of research potentially stand to benefit mankind and may be a source of pride for Canada!”
1974 — The final report of the MacDonald Stewart Foundation rejected the somatid theory and Naessens’ notion of bolstering the immune system to fight cancer. It now became apparent that Perey, who was to be the chief investigator, had been assigned other duties that effectively used up the time to run the Naessens study. This duty was passed on to a husband-and-wife team of researchers who were not in the least interested in truly researching the brilliant theories of Naessens. Their focus was only on one large form of the somatid cycle that had been described as a bacterium by German researchers who had isolated it in the 1930’s. Overall, they dismissed the stages of the somatid cycle as “artifacts” produced by mistakes during the process required to observe them. Perey’s response in relation to the researchers was, “microbiological dogmas are so entrenched in this couple’s minds that they do not allow themselves the luxury of challenging them.”
Late 1974 — Dr. Raymond Keith Brown, a consultant for New York’s Memorial Sloan-Kettering Cancer Center visited Rock Forest. Brown’s memo to the center read,”What I have seen is a microscope that reveals with spectacular clarity the motion and multiplicity of pleomorphic organisms in the blood which are intimately associated with disease states. The implications…are staggering….It is imperative that what its inventor, a dedicated biological scientist, is doing, and can do, be totally reviewed. I am convinced that he is an authentic genius and that his achievements cut across and illumine some of the most pertinent areas of medical science. If the review of his work is confirmed, this man should be brought to New York and given unlimited support and facilities to continue his research.”
Dr. Brown, along with an oncologist and microscopist eventually drafted a second memorandum that reiterated the first. Unfortunately, Naessens’ name appeared on the American Cancer Society’s “blacklist” and the excitement subsided.
August, 1980 — Naessens supplied 714-X to Dr. Gaetan Jasmin, a professor of pathology and medicine at the University of Montreal who was willing to embark on the standard animal-control test; that is, injecting the 714-X into cancerous and noncancerous rats. Dr. Jasmin concluded the substance had no effect and the results were reported in the MacDonald Stewart foundation literature in 1982. But, Jasmin refused to follow Naessens specific protocol for the use of the substance. He had injected the medicinal into the tumors themselves rather than into the lymphatic system, a procedure he decided was impossible. Whereas standard cancer treatments follow that procedure, Naessens’ truly holistic approach was designed to treat the symptom via the cause — the diametrical opposite of orthodox oncological approaches.
Throughout the 1970’s & 1980’s, doctors and patients alike continued to flock to Rock Forest. The doctors learned about the new biology, while the suffering patients were taught to inject themselves with 714-X or referred to doctors who were willing to treat them. Tremendous results continued as well.
December, 1984 — The police and officers of the Quebec Medical Corporation raided Naessens’ house and laboratory, seizing vials of 714-X and some 150 medical files. Charges would be brought some 5 years later.
1989 — Naessens was brought to trial. Despite the odds, he was acquitted. Witness after witness took the stand to describe the horrors of their battles with cancer and the hopelessness with Western treatments, and the cures they’d finally achieved using Naessens’ treatment. Imposing figures such as the politician Gerald Godin and the French ambassador to the Seychelles spoke passionately on Naessens’ behalf. Even the Quebecois folk hero, Gilles Vigneault showed his support. To the press, Vigneault described what was happening to Naessens as a “witch hunt” and went on to sing the praises of alternative medicine. He concluded: “One must seek, on humanity’s behalf, medical progress unblocked by pharmaceutical lobbyism that, together with that on arms mongers, is one of the world’s most powerful.” The headlines of the Journal de Montreal read “Naessens Acquitted.” A sidebar noted “It’s 25 years now that this farce has continued!”
Late 1990 — After receiving the positive results of nontoxicity tests, Health and Welfare Canada agreed that 714-X could be supplied by Naessens to doctors whose patients were suffering from terminal cancer.
1992 — A growing interest in Naessens’ approach to cancer, AIDS and other such diseases continues to grow. As of October of this year, 210 MD’s across the country (Canada) were administering it to patients. Naessens was also invited to the controversial conference on alternative treatments for AIDS held in Amsterdam in May. This conference was attended by such notables as Luc Montagier, the French scientist who is credited with the discovery of the so called “AIDS virus.” In Europe, the Philippines, New Zealand, Australia and the U.S., physicians are using 714-X with the conclusion that barring total destruction of the immune system, this may be the most promising treatment for AIDS and cancer ever seen. In the U.S. an independent study on 714-X using human patients has been under way since last May.
Commentary
It is very disheartening to see such abuses heaped upon such a brilliant, humane individual. One is reminded of the famous Hindu quote, “In shallow men, the fish of little thoughts cause much commotion. But in the oceanic minds, the whales of inspiration make hardly a ruffle.” However unfortunate, history is filled with such examples of “shallowness.” As Christopher Bird pointed out, the individuals who paved the way for Mr. Naessens — Antoine Béchamp, Geunther Enderlein, Royal Raymond Rife, Wilhelm Reich to name a few — met with similar abuses by the established medical authorities. Nonetheless, much interest continues to be generated by the man who someday will be recognized as another Albert Einstein.
Mr. Naessens’ work is at the forefront of a “new” push in health care; that is, prevention and bolstering the immune system via natural means. For example, AIDS, a disease characterized by subcellular organisms in pursuit of growth due to the presence of a deficient host {personal conclusion}, has been shown to be responsive in some instances to such immune enhancement approaches, particularly when compared to orthodox treatments.( 1) One hopes that future research and grants will begin to focus on this neglected aspect of health care. Also, one hopes that individuals such as Gaston Naessens will have the freedom and opportunity to continue their brilliant work in the field.
Note: Much of the material in this letter can be found in Christopher Bird’s book, The Persecution and Trial of Gaston Naessens. It is an excellent account of the work done by Mr. Naessens. I would also like to thank Mr. Bird for his input into this present article.
(1.) Culbert, Michael. AIDS: Terror, Truth and Triumph. R.W. Bradford Foundation: Chula Vista, CA, 1989.
Townsend Letter for Doctors & Patients.
_____________________________________
CANCER, 714-X AND GASTON NAESSENS
If you looked into a regular microscope at a drop of blood, the way it is done in most laboratories, you would see a still-life picture of bright-red cells, reddish-pink and purple cells. The sample of blood has been treated with dye to illustrate the different cells and nothing moves in this picture.
However, if you looked into a high-powered new microscope called a Somatoscope, invented by an exceptional French-Canadian, Gaston Naessens, you would see a totally different picture. Things move on a black background, seeming to bounce and bump around, and you would wonder if you could see twinkling before your eyes. The `twinklings’ that you see are not your imagination; they are called `Somatids’, and they can illustrate your life force and your state of health. Many conventional medical authorities don’t know what to make of it; some deny it; some admire it; some look the other way.
An investigative reporter with a deep-voiced Georgian drawl, author Chris Bird, told the audience at Health Action ’91 of his investigations into the life and work of the French-Canadian inventor Gaston Naessens. With his natural investigative spirit, he discovered a fascinating story of the suppression of a genius, and the gift that this genius has offered to an unwilling medical community, a new cancer treatment called 714-X.
This new microscope is being used as part of a program for cancer patients available to Canadians. After deciding that 714-X is a treatment that the patient would like to pursue, then it is necessary to convince the medical doctor this is the treatment of choice. Having established that, then the physician is to notify the Emergency Drug Program in Ottawa at (613) 993-3105. A history of the patient is required, and the serum and instructions on administering it will be sent directly from the Naessens clinic to the doctor. Details on how to obtain the Somatoscope, or requests for information, can be addressed to: The Naessens Clinic C.O.S.E. 5270 Fontaine Rock Forest, Quebec J1N 3B6 or telephone (819) 564-7883 or FAX (819) 564-2195. Or, send $15 to HANS [to help cover costs] and we will send you an information package on this topic.
Health Action Network Society.
By Christopher Bird
_____________________________________
A New Answer to Cancer: Microbiologist Gaston Naessens’ immune system therapy 714X has been achieving dramatic results — and irking the “cancer industry.”
Thirty-nine-year-old Jacques Viens had gone home to die. Seven-eighths of his stomach had been removed, and the cancer had already spread to the lymph. Since there seemed to be no hope of recovery, his doctor offered him a new, experimental treatment called 714X. He tried it. Four months later he was healthy enough to go hunting, and not long after that he resumed his job.
Fifty-one-year-old Marcel Caron suffered from intestinal cancer, but he refused to have his intestine removed. His wife’s breast cancer had been successfully treated with the same experimental medicine Viens had used; Caron wanted to try it too. Sixty-five days after he started treatment, no cancer was to be found in Caron’s body. Eight years later, he was still healthy.
These are just two among hundreds of case histories of patients who recovered using a little-known approach to cancer and other degenerative diseases that proponents claim could revolutionize medical practice. The first person to use it — more than 20 years ago — is still alive.
What would happen if an effective treatment for cancer were finally found — a nontoxic, natural, and inexpensive treatment that could be self-administered at home with a success rate of 75 percent? It sounds like a dream come true, a miracle. We would all breathe a little easier, that’s for certain; many lives would be saved.
And a multibillion-dollar enterprise — the pharmaceutical-medical-insurance complex, the most profitable industry in America today — would be forever transformed. Dozens of giant pharmaceutical and medical supply companies would be forced out of business. The “cancer industry” would be no more.
Little wonder, then, that we have heard so little about a 69-year-old French microbiologist who says he’s discovered such a treatment. His name is Gaston Naessens, and he calls his immune-system therapy 714X.
When Naessens’ unorthodox treatment methods began yielding dramatic successes in his native France, French medical authorities closed his lab, confiscated his equipment, and heavily fined him for practicing medicine without a license. Naessens went to Canada, where, with the help of the prestigious MacDonald Foundation (which for years has funded cancer research), he set up a small laboratory outside Montreal. There he and his wife, Francoise, continued their careful research until 1989, when Naessens was again brought to trial by the medical authorities, accused of contributing to the death of a woman who did not recover after using his treatment.
After a long trial, in which numerous testimonies were offered by patients and physicians using his approach, he was finally acquitted. (The full story of the trial is told in Christopher Bird’s book The Persecution and Trial of Gaston Naessens.) Now, a handful of doctors are struggling to make Naessens’ controversial treatments readily available in the United States.
Born in northern France in 1924, the young Naessens was a precocious inventor who built a small, functioning automobile-type vehicle when he was only five, followed by a homemade motorcycle. By the age of 12 he had constructed a plane that could fly. (His mother burned it to prevent him from flying it, however.)
When his university studies of physics, chemistry, and biology were interrupted by World War II, Naessens earned an unofficial diploma from the Union Scientifique Francaise in Lilies, where most of his university professors had fled to escape the Nazi invasion. (He never bothered to pursue its formal equivalent after De Gaulle restructured France, a decision that would later lead to accusations that he lacked a college degree.)
With his mother’s support, Naessens continued his studies on his own. While pursuing the study of hematology, he observed “something moving in the blood,” but the particle was too small to be identified by the optical methods he had at his disposal. Fascinated, Naessens enlisted the help of optical specialists in Germany in developing a stronger microscope.
Called the somatoscope, the microscope itself was a significant scientific achievement. Using a unique combination of incandescent and ultraviolet rays, it allowed him to look at living blood (without first fixing and staining it, which is the usual method) at a magnification of 30,000 times with a resolution of 150 angstroms — a capacity that has not been exceeded to date.
Using this unique method of microscopy, Naessens was able to study what he had glimpsed previously but could not identify: motile microorganisms in the discovered that somatids are resistant to acids and bases as well as heat and that they cannot be cut with a diamond. For example, they withstood 2 megarads of radiation capable of killing any living thing, as well as carbonization temperatures of over -200 C. He concluded that they are indestructible.
Recently, Dr. James F. Ransdell, a pathologist on the faculty of the University of California at Davis, showed me the somatids in my own blood on a TV screen, using Naessen’s “condenser,” an attachment he developed that converts a regular microscope into one resembling his invention. Lots of bright little bodies were busily circulating around the red blood cells, platelets, and lymphocytes in my blood, their motion not unlike that of swarming bees.
Cell division cannot take place without these busy, glowing bodies, Naessens postulates, because in the course of its cycle the somatid releases the growth hormone trephone, which enables cells to divide and multiply. Naessens goes even further — he believes the electrically charged, luminous somatid is the original spark of life, the pinpoint where energy condenses into matter. According to Naessens, the somatid represents the manifestation of cosmic energy in a tiny, moving dot of physicality.
quently attributed to environmental toxicity, by rejuvenating the body’s defenses. Holistic treatments, like the traditional methods from which they evolved, consist of appropriate diet, exercise, and supportive plant medicines to replenish our depleted reserves and restore strength.
Naessens’ theories align with the tenets of holistic practice. But unlike most holistic healers, Naessens is able to provide scientific documentation and evidence of what traditional and naturopathic approaches have suggested all along — that disease represents imbalance in the ecology of the whole organism.
In healthy individuals, says Naessens, the somatid moves through a three-stage cycle that produces the right amount of the growth hormone trephone to keep cells reproducing at the appropriate rate. (This growth hormone was first identified by Nobel laureate Alexis Carrel, who did not, however, link it to a subcellular entity in the blood.)
When the body is stressed or weak, however, the somatid shifts into a longer macrocycle that features 13 additional stages, including forms that resemble bacteria, viruses, and yeast cells. Other scientists have seen some of these forms in the blood of cancer patients and have posited a bacterial and, later, a viral cause of cancer. However, according to these theories (which have not been confirmed by scientific evidence), the disease carrier has always been thought to enter the body from somewhere outside, as germs do. In Naessens’ view, these microbial forms are simply phases of the somatid in its extended cycle. In this amplified cycle, the somatid produces excessive quantities of growth hormone, creating the abnormally rapid cell growth we call cancer.
Naessens is not the first scientist to describe polymorphic entities in the blood. In the early 1800s, Antoine Bechamp, like Guenther Enderlein and many other pioneers, using far more primitive microscopes than Naessens’, perceived microzymas, or “little bodies,” which were thought to be fundamental elements of cells and whole living organisms. When the organism is disturbed by a serious event, Bechamp theorized, the symbiotic relationship between the microzymas and the body becomes imbalanced, leading to disease. In this view, illness originates within the body.
The scientific establishment rejected Bechamp’s work in favor of that of Pasteur, who was convinced that disease is caused by bacteria entering the body from without. Pasteur’s work, which had wide application to a host of infectious diseases, led to the important discovery of immunization. Bechamp’s theory was rejected, and germ theory became a sacred tenet in medicine, despite the fact that a number of diseases do not appear to conform to that pattern. On his deathbed, Pasteur was said to disavow his own theories and exclaim, “[He] is right. The microbe is nothing! The terrain is all.”
In Naessens’ theory, the microcycle of the somatid is held at three stages by blood inhibitors, which consist of certain digestive enzymes, hormones, and minerals. Poor diet and stress apparently reduce the number of blood inhibitors, allowing the somatid to commence its extended 13-phase macrocycle. The presence of these extra somatid forms signifies the beginning of degenerative disease before it has manifested itself in the body. Hence the somatid theory has a valuable diagnostic application, which, in combination with other factors, makes it possible to diagnose and even treat the disease before it takes hold.
The difference between healthy cells and cancer cells is their rate of growth. The somatid macrocycle generates a tremendous increase in the number of somatids, releasing more and more growth hormone into the body and stimulating the rapid multiplication of cells we call cancer. The increasing mass of disorganized cells secrete what Naessens has called the “co-cancerogenic factor,” a substance that allows the cancer to withdraw essential nitrogen derivatives from the patient’s cells and also begins to paralyze the immune system, radically undermining the patient’s ability to combat the disease.
The cancer does not take long to metastasize (spread to new locations) throughout the body. Since the usual orthodox methods of treating cancer involve cutting out, burning, or poisoning the cancerous tumors, cancer’s potential to metastasize has kept everyone stumped. A systemic treatment for the disease would enable the body to again perform its normal function of removing cancer cells, which in healthy bodies takes place almost daily.
According to proponents of the approach, Naessens’ 714X (the name is alpha numerological reference to the letters in his own name) is such a treatment. It is distributed rapidly throughout the body by the unique method of intra-lymphatic injection. Doctors have said such injection is physiologically impossible, due to the structure of the lymphatic system — yet thousands of people have now used the treatment with encouraging results.
714X is an aqueous solution (trimethyl bicyclo mino heptane-CL) consisting of camphor, mineral salts, and nitrogen salts, which is injected once a day for a 21-day cycle. The treatment is then repeated until the progress of the disease is reversed and finally stopped.
The salts help to cleanse and clear the lymph of toxins accumulated during the disease, thereby reviving the body’s defenses, which go back to work to fight the cancer. The nitrogen actually feeds the cancer cells so they do not drain the body’s nitrogen. The camphor carries the nitrogen to the cells and impedes the formation of the “co-cancerogenic factor,” again stimulating the body’s own ability to fight the disease.
(Camphor is widely used by village people throughout India to treat a wide variety of illnesses, from bronchitis to diarrhea. According to Jahnavi Morton, an ayurvedic practitioner who studied under Vasant Lad in New Mexico, camphor is used for “opening the flow of prana, bringing clarity to the mind.”)
A healthy diet that follows the familiar guidelines of holistic nutrition (no sugar, low fat, no dairy, no pork or beef, and so on) accompanies the treatment.
Unlike allopathic medicine’s “magic bullet” approach to illness, the treatment does not do anything directly to the malfunctioning somatid, nor does it attack the symptoms of the disease. All it does is stimulate the body’s ability to regain its balance and defeat the cancer on its own. A healthier organism produces more blood inhibitors, slowing down the somatid cycle. As a result, the amount of growth hormone (responsible for cell division) produced by the somatids begins to decline, so cancer cells do not multiply as quickly. Meanwhile, the body’s ability to destroy the existing cancer cells increases. The cancer does not spread. The tumor begins to regress. The body regains its natural balance. The progress of the disease is reversed until it disappears.
Among the growing number of physicians who are recognizing the efficacy of 714X is Dr. Dietmar Schildwaechter, a former faculty member of the University of Pennsylvania School of Medicine who now directs a cancer rehabilitation center in his native Germany. He came across Naessens’ treatment in 1990 through one of his own patients, who showed marked improvement when, unbeknownst to him, she began taking it. When he found out what she was taking, he began looking into the unconventional treatment himself. He “realized that Naessens had discovered and identified what others had only partially seen.”
“Gaston Naessens’ discoveries,” Schildwaechter writes, “represent a brand new dimension in medicine. His recognition of the somatids as the basic form of life and his furnishing a microscopic means to monitor their cycle are nothing short of revolutionary. His method, offering an instant and highly refined way of assessing every human being’s state of health and their responses to therapy, is second to none.” Schildwaechter is now the chief investigator of the Institutional Review Board (IRB) that is documenting the successes of 714X with the goal of obtaining FDA approval for its use in the United States as an experimental treatment.
Naessens’ treatment continues to be available by doctor’s prescription, so long as the patient is willing to sign an informed consent for the administration of an unapproved drug. In order to be thoroughly familiar with the treatment, all patients (and doctors) should be required to read Do No Harm, a protocol booklet published by Writers and Research, Inc.
Although Naessens boasts a 75 percent rate of success for his unique treatment, how are we to know that this is not just another crackpot cure? Most alternative treatments lack the validation on which Americans have come to rely, the stamp of approval by the American Medical Association, the National Cancer Institute, and the FDA. The august bodies of medical research have demonstrated a reluctance to investigate therapies that have not emerged from their own labs.
Of the 63 treatments on the “list of unproved methods” published by the American Cancer Society, over 40 percent have never even been investigated by the medical establishment, writes Ralph Moss, author of The Cancer Industry. “Merely including a scientist’s name on the list of unproven methods has the effect of damning that researcher’s work and putting a tag of quackery on his efforts.” Gaston Naessens is number 63 on that list. American medical authorities, it seems, have joined the French and Canadian in blacklisting his research.
People like Bird and Schildwaecheter argue that there is sufficient evidence that this treatment should be thoroughly evaluated, not dismissed out of hand — specially considering the tremendous toll taken on the body by conventional approaches like chemotherapy, surgery, and radiation. Great scientific advances have often come from off the beaten track, they argue, the work of brave innovators who have neither the time nor the patience to keep their credentials up to date with established boards. The somatid theory may be one of them.
But the most powerful argument for making Naessen’s treatment available is the example of people like Anne Vignal, wife of the former French Counsel General in Quebec, who went to medical doctors to find out why she had not conceived. They told her her infertility was due to a lethal form of leukemia and that she had only three to five years to live.
Vignal had the good fortune to learn of Gaston Naessens and his ground-breaking work. Five years after being treated with 714X, she is very much alive and cancer-free — and the mother of a healthy son.
Yoga Journal L.L.C.
By Stephanie Hiller
Source: Dr Gaston Naessens - Cancer Cures Plus
Book with a chapter dedicated to Gaston Naessens on page 115:
Education of Cancer Healing Vol. VII - Heretics
Gaston Naessens and 714-X
I have grave doubts about Naessens work.
A crusty old man, undoubtedly a genius, but the somatid hypothesis is rather wild.
It was very hard trying to work with Naessens - in fact impossible.
I sold my microscope in 1999 and have not done any work in this field since then.
Back then we tried to set up a research project - some of the top medical and scientific minds were involved, but Naessens effectively scuttled the project.
So, take a look at my bottom line
Towards a bottom line
and meanwhile...
The following is what I thought in my first enthusiasm...
Gaston Naessens is responsible for several remarkable developments which may revolutionise our understanding of life and bring a major advance in cancer therapy. His work started with the invention of an amazing microscope, the "somatoscope". This led him to the discovery of the Somatid Cycle, and in turn to the development of his serum, 714-X.
The Somatoscope
Naessens' revolutionary microscope, the somatoscope, weaves two light sources (one visible, one ultraviolet) together to produce a third, functionally higher, frequency with which it is possible to obtain a resolution and magnification thirty times greater then with conventional light microscopy . (In conventional light microscopy resolution, and therefore magnification, is limited by the wavelength of visible light - approximately 4000 Angstroms.) Although with the electron microscope there is almost no limit to the magnification, the electrons must be beamed through a vacuum, so it can not be used to look at living material. Naessens' remarkable somatoscope, however, can view live material with a resolution of 150 Angstroms, a magnification of 30,000 diameters. That magnification reveals a whole new world in a tiny drop of blood. The world that Gaston Naessens sees in that drop with his somatoscope is quite different from what we were taught at school! He sees that our blood is alive with a teaming micro-ecology. This is how Gaston Naessens discovered the somatid.
Somatids
In all living plants and animals Naessens observed tiny creatures. He called them somatids - "little bodies". He says that in the healthy organism the somatids have a simple three stage life cycle (a simple viroid form, spores, and double spores). This he named the microcycle. The somatids are symbiotic - they've always been with us, and we need them. However, when the body is under stress the somatids elaborate into a more complicated macrocycle, a sixteen stage cycle. The macrocycle is parasitic and is associated with the development of immune compromised diseases - such as cancer. Naessens' theory is that there are inhibitors in the blood that keep the somatids in the healthy symbiotic microcycle. Under stress these inhibitors may be lost and our friends, the somatids, turn into opportunistic parasites. So, in the 16 stage macrocycle bacteria-like and fungus-like forms grow from the somatids. This elaboration of forms is termed pleomorphism. The somatid pattern can function as an indicator of serious disease. The somatid pattern associated with cancer, for instance, is usually observed in the blood up to two years before the manifestation of the disease. This allows us to get a really early warning when we are headed for trouble or it can be helpful in keeping track of the progress of a preexisting disease. By monitoring the somatid phenomenon we can observe a patient's response to both orthodox and alternative treatments, and to life style changes.
Pleomorphism and Darkfield Microscopy
Although developed in isolation, Gaston Naessens' theories are part of a larger body of work that we may call "the darkfield work". His somatoscope is a very special variation of the darkfield microscope. All those who have worked extensively with darkfield microscopy, with live blood, have come up with similar stories of pleomorphism. In conventional "brightfield" microscopy we send light directly through the specimen, and so we can't see the specimen (thin slices of tissue, including blood, are transparent) unless we stain it canadian propecia. And to stain it we have to kill it. So again, as with the electron microscope, orthodox science, with all its sophistication, looks at dead material. With darkfield microscopy light is shone onto the specimen from the side. We look at reflected light against a dark background. This gives us a highly contrasted image. We don't need to stain the specimen, and therefore we can examine at living material. The darkfield microscope allows us to observe the somatid's pleomorphic cycles.
One of the first scientists who talked about pleomorphism in human blood was Béchamel, a contemporary and rival of Pasteur. He called the little bodies he observed "microzymes". Enderlein in the first half of this century called them "protits". In the 1930s Rife built a darkfield microscope comparable to Gaston Naessens'. He too saw pleomorphism.
Pleomorphism is a natural adaptive response of microorganisms. When the environment allows they are virus-like, bacteria-like, or fungus-like: they metamorphose to suit their conditions. When we are healthy they help us. According to Naessens they produce a growth hormone that is essential for cell division in all plants and animals. Biologist call this sort of mutually depended relationship "symbiosis". However, when we are unhealthy our friends, the somatids, turn on us and become parasitic. But this parasitism is a process that can be recognised by darkfield microscopy and it can often be reversed. Most important, we must find out what stressors caused the problem, and correct the situation.
714-X
Gaston Naessens' next invention was the development of a treatment that he calls 714-X. 714-X is a nitrogenized camphor derivative (trimethylbicyclo-nitraminoheptane). As I understand it the rationale behind this treatment is as follows: Gaston Naessens learned that tumours are nitrogen traps. They steal nitrogen from the body and this inhibits the immune system. By supplying nitrogen to the tumour and the body, the immune system is disinhibited, and the body begins to heal itself. (Camphor has a natural affinity for tumours and, as it is not toxic at pharmacological doses, it proved to be the perfect vehicle to carry the nitrogen to the tumour and the body.) The serum is injected "paranodularly" - that means next to the lymph nodes - so it is absorbed into the lymphatic system where it can act most directly. People close to Gaston Naessens' work believe that 714-X is best used early. While they believe it may save one in twelve of the terminally ill patients who turn to it on their death beds, and maybe one in six of the advanced cancer patients who try it as a last hope, when it is given early in the disease process, they feel that it might help almost everyone. Further, anecdotally, even in advanced cancer, 714-X may greatly improve quality of life.
The normalization of immune function is not only of benefit with cancer; 714-X is also thought to help to stabilize, though not to cure, AIDS, and to be of benefit with other disorders in which the immune system is compromised. To date no adverse reactions or side effects have been observed beyond some irritation at the site of injection.
In 1990 714-X was made available through Health and Welfare Canada's Emergency Drug Release Program and it can now be ordered by any MD. More than 800 patients have received 714-X, and it has recently been transferred from experimental to investigational status.
Gaston Naessens' remarkable work promises a whole new understanding of biology. It leads to a new perspective and, hopefully, a great advance in cancer treatment.
To make his work more widely accessible Gaston Naessens has designed a modified version of the darkfield condenser that allows the observation of the somatid cycle that he discover with his somatoscope. Under the banner of "The Canadian Institute of Alternative Medicine" I purchased Naessens darkfield system and offer the "somatid observation" in Toronto. Phone 416 928 9272 or email normanallan
Darkfield microscopy brings us a window into the body and a road to a new understanding.
Norman Allan, Ph.D., is a research scientist and practitioner of alternative therapies based in Toronto. For more information phone 416 928 9272.
Towards a bottom line
2007: when I was first using the microscope in 1994, I would often damage the sample to one extent or another. Then all sorts of monsters might appear in the sample. Were those Naessans' medusaheads?
Something 's going on. I must write of my encounters with pleomorphism.
While I was learning to use the darkfield techneque I helped initiate and was involved in a wonderful collberative effert with some of the brightest lights in the oncology and academic community and Naessens stepsons (who were wonderfully open, bright, and competant) to study 714X, say in lung cancer, but Naessans said "Non".
Meanwhile my friend Ralph had an enthusiastic encounter with 714 and Gaston that faded when data wasn't open. There are no clinical trials, there is no good data, and that seems to be because of Gaston...
so to me 714-X walked off into the distance,
but pleomorphism?
Bottom line?
714-X is not toxic. For many patients with enthusiasm for the product it has been a blessing, but there is no knowing how many. Naessens was not open and there is no good data on the effectiveness of 714-X.
Quite a number of people call me about 714-X, but there is nothing more than the above (except for some gossip) that I could tell them...
Appended information:-
The Somatoscope: "Two light sources, one incandescent with a wavelength of 3,300 angstroms, the other ultraviolet of 1,850 angstroms, start pulsating, producing a third wavelength. This wave goes through a monochromator which produces a ray. This ray is exposed to a magnetic field (the Zeemann effect) which splits it into parallel rays. One of these rays is treated by a Kerr cell which increases its frequency. This cell is then stimulated by a step generator-oscillator at frequencies which vary from 250 to 1,200 megahertz. The modulation of a visible light frequency ranging from 250 to 1,200 megahertz produces a basic frequency ranging from 250 to 1,200 megahertz, but also harmonics at a higher frequency (if we use light in the order of 2,000 �). ... the resolution of this instrument is in the order of 150 � and the power of its magnification varies from 2,000 to 30,000." (Gaston Naessens)
Pleomorphism: In a scientific article published in 1992 it was shown that yeast, starved of nitrogen, undergoes pleomorphic transformations. This work both parallels darkfield's pleomorphism and vindicates Naessens' rationale for 714-X. (Gimeno et al. Unipolar Cell Division in the Yeast S. cerevisiae Lead to Filamentous Growth: Regulation by Starvation and RAS. Cell 68:1077-1090. March 20,1992)
Cancer and Pleomorphism: "The number and forms of the bacteria seem to mirror the state of systemic sickness in cancer patients, and, by following the appearance of the blood by darkfield microscopy, the patient's therapeutic progress can be monitored." Macomber. Cancer and Cell Wall Deficient Bacteria. Medical Hypotheses 32, 1-9, 1990.
Read full article, with accompanying images and references at: http://www.normanallan.com/Med/714.html
THE SOMATID THEORY AND PLEOMORPHISM
by Dr. Lawrence Wilson
© May 2016, L. D. Wilson Consultants, Inc.
All information in this article is for educational purposes only. It is not for the diagnosis, treatment, prescription or cure of any disease or health condition.
This is one of the more unusual articles on this website. The science is not proven, but please have an open mind. I am hardly the first person to write about this topic.
The somatid theory can definitely help explain newer medical findings that the human intestine is producing many vital chemicals such as hormones, vitamins, and immune system components.
Definitions. Somatids are a type of small, less differentiated body cells found everywhere in the human and animal bodies. Most live in the small intestines, and most are made by mitosis in the brain.
Mitosis means a cell splits into two small ones.
Similar to trophoblasts. In size and functioning, somatids are similar to Trophoblast Cells, discussed in a separate article on this website.
Totipotent. Trophoblasts are almost totipotent cells. The word totipotent (total potency) means they can turn into any other kind of cell. Somatids are similar to this and may be the same, in fact.
Generalists. Most cells, early in their lifespan, differentiate. To differentiate means the cell becomes a specialist. Some cells become stomach tissue, while others become skin or hair. Others become the eyes, the nose, or some other body tissue. The cell remains this way for the entire life of the cell. Somatids, in contrast, can change their form and their functions.
Pleomorphism. The quality of changing one’s form and function is called pleomorphism. The word just means having many forms. So one can say that somatids are pleomorphic. This just means that they can change their form and function.
DISCOVERY OF THE SOMATIDS
Somatids were first found in modern times about 110 years ago when several European scientists with special microscopes noticed them. One needs a special microscope because most microscopes, including the most modern electron microscopes, require killing cells first before you can look at them.
If one kills the somatid, one will not see the cell change its form or function. As a result, the idea of a cell that changes itself depending on its environment is not currently accepted in medical science.
The scientists who discovered somatids had special microscopes, known today as Rife microscopes. These are very rare instruments, and there are very few of them on earth. They turn the specimen into a light source, and as a result can get extremely high resolution on a live cell.
The somatid discoverers. The first scientist to see them was Antoine Bechamp, MD (1816-1908) in France. He called them mycozyma. Some people still use this term, but most prefer the word somatid. He saw that they changed their form depending on the terrain inside the body.
As a result, he believed they were the basic building blocks of all organisms, even plants and rocks. In this, I believe he was incorrect. Not all cells are somatids. However, he was correct in identifying the somatids as very unusual.
In the early twentieth century, several other scientists observed them. A Canadian doctor, Gaston Naessens, MD (1924- ) called them somatids. Guenther Enderlein (1872-1968), a German physician, called them protits. The name somatids is most accepted.
Another who observed them was Royal Rife, MD in the United States. All these scientists wrote about these cells, and designed remedies based upon them, as well. To read more about Dr. Rife, Dr. Naessans and pleomorphism, read The Cancer Pioneers on this website.
MODERN SCIENCE DOES NOT RECOGNIZE SOMATIDS
The concept that a cell can change its basic form has found only limited acceptance in the medical world. For example, it is known that many yeasts are dimorphic. This means they have two forms.
They have both a mold or hyphal form, and a yeast form. Among such yeasts are some penicillins and the common candida albicans. Somatids are somewhat like this – able to change their form depending on the conditions inside the body.
The medical establishment considers somatids part of esoteric or occult science, but it is no such thing. It is simply science that is more advanced, or harder to see.
SCIENTISTS DISCOVERING THAT THE GUT DOES MORE THAN DIGEST FOOD
One of the more modern discoveries of medical science that is mostly still unknown among doctors is that one’s intestine is not just a place to digest food. It contains immune cells, and many others. This may be because of the presence of the somatids.
In fact, a popular diet for autistic children is called the Gut And Psychology Diet or GAPS diet, for this reason. To read more about this, and why I don’t recommend it, please read The GAPS Diet on this site.
ARE THE PLEOMORPHIC FORMS PATHOLOGICAL?
Gaston Naessens and other researchers believed that the pleomorphic forms of somatids are abnormal and pathological. This appears to be true, although some scientists debate this point.
ARE SOMATIDS THE SAME AS PROBIOTICS?
No. The somatids are not the same as what are called probiotic organisms. The latter include various strains of bacteria such as lactobacillus acidophilus, for example. These are cells that cannot change their form or function. In contrast, somatids can change their function.
The somatids are also different from what are called ferments in the intestines. These are various bacteria and yeasts found in foods such as yogurt, sauerkraut, miso, cheese, kefir, and a few other foods. Differences between somatids and probiotics include:
1. Compared with the souls in bacteria and ferments, the souls in the somatids are much more advanced.
2. Somatids are not just found in the intestines, as are the probiotic organisms. Somatids are found everywhere in the body.
3. Somatids can move in and out of body organs easily because they are extremely tiny. Probiotic organisms are much too big to be able to do this.
These are just a few of the differences between somatids and other micro-organisms in our bodies.
IMPORTANCE OF FIXING THE TERRAIN OF THE BODY
The implications of the somatid theory are enormous, including the following:
1. If the terrain of the body is this important, then diet, lifestyle, rest, sleep, thoughts and emotions should be the focus of our health care system, not drugs, surgery, vaccines, fluoridation and other toxic methods.
2. If terrain is important, detoxification of the body is critical, as nutritional balancing asserts.
3. If terrain is critical, then keeping the body pure in all ways should be the goal. In addition to a pure diet, one’s lifestyle, morals, character development and careful education of the young are therefore of the greatest importance.
FINAL REPLACEMENT OF THE SOMATIDS
If a person follows a nutritional balancing program for at least 20 years, causing development, the somatids atrophy, and eventually disappear. This may occur when the down force through the body is strong enough. To read more about this, please read Downward Moving Energy And Healing on this site.
The replacement of the somatids is one of the goals of every nutritional balancing program. However, to the best of my knowledge, final somatid replacement is not discussed among doctors who endorse pleomorphism and the somatid theory. Most likely, this is because they do not know how to accomplish the replacement of the somatids.
Source: http://drlwilson.com/articles/SOMATIDS.htm
Manufacturer's webpage with multiple official company YouTube videos which are hidden on YouTube itself, about 714X, a screening test, somatid and its pleomorphism and the somatoscope:
Media | Cerbe Distribution Inc
Basically this is a cancer medication which has to be administered by a doctor in Canada or Mexico and has a big success rate to date according to sources. The 714X (the anti-cancer agent) product is still manufactured, with cGMP quality, sold and used by clinicians to this day in Canada and Mexico. The somatoscope is still in use by scientists, so far as sources state. The 714X product can be found on the manufacturer's website here:
Cerbe Distribution Inc | A Trustworthy Partner for Better Health
Mr Naessens has sadly passed away this year at the age of 94.
French news article about his passing: Le chercheur Gaston Naessens n’est plus
I hope this topic will be used to discuss the works of Mr. Naessens and his cancer treatment and that it will help people when it comes to cancer treatment options and discussion.
CC: @burtlancast (From who I came across Naessens and 714X, thank you for that, Burtlancast!)
President of CERBE inc.
I am the biologist researcher engineer who developed a unique optical instrument, the Somatoscope, capable of observing unstained living matter, allowing me to discover a new particle alive in fresh human blood, that I have called the somatid . Thanks to the discovery of the somatid, at the origin of degenerative diseases, and its importance in many biological functions such as cell division and the transmission of genetic characteristics, I was able to develop the somatidian theory and to bring new responses to diseases affecting the immune system. As the designer, manufacturer and President of CERBE Inc. and CERBE Distribution Inc., I embody the innovative and human vision of health that I propose in my harmonious biological approach which can be curative as well as preventive.
Fundamental research in optics and biology (virology and hematology) have fascinated me for over 60 years, and I actively continue my experiments and development of innovative and non-toxic health products aiming to rebalance the immune system, like 714X. This is my mission in life!
Read more at: Our team | Cerbe Distribution Inc
The Earthshaking Discoveries of Gaston Naessens:
- A microscope that permits practitioners to view living matter at degrees of resolution far greater than state–of–the–art microscopes currently available.
- The Somatid, an ultramicrosopic subcellular living and reproducing entity, which many scientists believe is the precursor of DNA and which may be the building block of all terrestrial life.
- The somatid cycle — visible in the blood of every human — which, when properly interpreted, can prediagnose degenerative diseases by up to eighteen months.
- 714X, a compound that has restored the perfect health of 750 out of 1,000 cancer victims and that has had equally dramatic effects with AIDS patients.
(This book and its Appendixes comprise important reading material that will help you understand "The Life Processes Here on Planet Earth". — Tommy)
Chapter 1
Discovery of the World's Smallest Living Organism
"When the great innovation appears, it will almost certainly be in a muddled, incomplete, and confusing form ... for any speculation, which does not at first glance look crazy, there is no hope."
Freeman Dyson, Disturbing the Universe
Early in the morning of 27 June 1989, a tall, bald French-born biologist of aristocratic mien walked into the Palais de Justice in Sherbrooke, Quèbec, to attend a hearing that was to set a date for his trial. On the front steps of the building were massed over one hundred demonstrators, who gave him an ovation as he passed by.
The demonstrators were carrying a small forest of laths onto which were glued, stapled, or thumbtacked placards and banners. The most eye-catchingly prominent among these signs read: "Freedom of Speech, Freedom of Medical Choice, Freedom in Canada!" "Long Live Real Medicine, Down With Medical Power!" "Cancer and AIDS Research in Shackles While a True Discoverer is Jailed!" "Thank you, Gaston, for having saved my life!" And, simplest of all: "Justice for Naessens!"
Late one afternoon, almost a month earlier, as he arrived home at his house and basement laboratory just outside the tiny hamlet of Rock Forest, Quèbec, Gaston Naessens had been disturbed to see a swarm of newsmen in his front yard. They had been alerted beforehand – possibly illegally – by officers of the Suretè, Quèbec's provincial police force, who promptly arrived to fulfill their mission.
As television cameras whirred and cameras flashed, Naessens was hustled into a police car and driven to a Sherbrooke jail, where, pending a preliminary court hearing, he was held for twenty-four hours in a tiny cell under conditions he would later describe as the "filthiest imaginable." Provided only with a cot begrimed with human excrement, the always elegantly dressed scientist told how his clothes were so foul smelling after his release on ten thousand dollars' bail that, when he returned home, his wife, Françoise, burned them to ashes.
It was to that same house that I had first come in 1978, on the recommendation of Eva Reich, M.D., daughter of the controversial psychiatrist-turned-biophysicist Wilhelm Reich, M.D. A couple of years prior to my visit with Eva, I had researched the amazing case of Royal Raymond Rife, an autodidact and genius living in San Diego, California, who had developed a `Universal Microscope" in the 1920s with which he was able to see, at magnifications surpassing 30,000-fold, never-before-seen microorganisms in living blood and tissue.*
*"What Has Become of the Rife Microscope?," New Age Journal, (Boston, Massachusetts), 1976. This article has, ever since, been one of the Journal's most requested reprints. It is reproduced in this book as Appendix A. Developments in microscopic techniques have only recently begun to match those elaborated by Naessens more than forty years ago
Eva Reich, who had heard Naessens give a fascinating lecture in Toronto, told me I had another "Rife" to investigate. So I drove up through Vermont to a region just north of the Canadian-American border that is known, in French, as "L'Estrie," and, in English, as `The Eastern Townships." And, there, in the unlikeliest of outbacks, Gaston Naessens and his Quèbec-born wife, Françoise (a hospital laboratory technician and, for more than twenty-five years, her husband's only assistant), began opening my eyes to a world of research that bids fair to revolutionize the fields of microscopy, microbiology, immunology, clinical diagnosis, and medical treatment.
Let us have a brief look at Naessens's discoveries in these usually separated fields to see, step by step, the research trail over which, for the last forty years – half of them in France, the other half in Canada – he has traveled to interconnect them. In the 1950s, while still in the land of his birth, Naessens, who had never heard of Rife, invented a microscope, one of a kind, and the first one since the Californian's, capable of viewing living entities far smaller than can be seen in existing light microscopes.
In a letter of 6 September 1989, Rolf Wieland, senior microscopy expert for the world-known German optics firm Carl Zeiss, wrote from his company's Toronto office: "What I have seen is a remarkable advancement in light microscopy. ... It seems to be an avenue that should be pursued for the betterment of science." And in another letter, dated 12 October 1989, Dr. Thomas G. Tornabene, director of the School for Applied Biology at the Georgia Institute of Technology (Georgia Tech), who made a special trip to Naessens's laboratory, where he inspected the microscope, wrote:
Naessens's ability to directly view fresh biological samples was indeed impressive ... Most exciting were the differences one could immediately observe between blood samples drawn from infected and non-infected patients, particularly AIDS patients. Naessens's microscope and expertise should be immensely valuable to many researchers.
It would seem that this feat alone should be worthy of an international prize in science to a man who can easily be called a twentieth-century "Galileo of the microscope."
With his exceptional instrument, Naessens next went on to discover in the blood of animals and humans – as well as in the saps of plants – a hitherto unknown, ultramicroscopic, subcellular, living and reproducing microscopic form, which he christened a somatid (tiny body). This new particle, he found, could be cultured, that is, grown, outside the bodies of its hosts (in vitro, "under glass," as the technical term has it). And, strangely enough, this particle was seen by Naessens to develop in a pleomorphic (form-changing) cycle, the first three stages of which – somatid, spore, and double spore – are perfectly normal in healthy organisms, in fact crucial to their existence. See figure:
The Somatid Cycle.
Even stranger, over the years the somatids were revealed to be virtually indestructible! They have resisted exposure to carbonization temperatures of 200º C and more. They have survived exposure to 50,000 rems of nuclear radiation, far more than enough to kill any living thing. They have been totally unaffected by any acid. Taken from centrifuge residues, they have been found impossible to cut with a diamond knife; so unbelievably impervious to any such attempts is their hardness.
The eerie implication is that the new minuscule life forms revealed by Naessens's microscope are imperishable. At the death of their hosts, such as ourselves, they return to the earth, where they live on for thousands or millions, perhaps billions, of years!
This conclusion – mind-boggling on the face of it – is not one that sprang full-blown from Naessens's mind alone. A few years ago, I came across a fascinating doctoral dissertation, published as a book, authored by a pharmacist living in France named Marie Nonclercq.
Several years in the writing, Nonclercq's thesis delved into a long-lost chapter in the history of science that has all but been forgotten for more than a century. This chapter concerned a violent controversy between, on the one side, the illustrious Louis Pasteur, whose name, inscribed on the lintels of research institutes all over the world, is known to all schoolchildren, if only because of the pasteurized milk they drink.
On the other side was Pasteur's nineteenth-century contemporary and adversary, Antoine Bèchamp, who first worked in Strasbourg as a professor of physics and toxicology at the Higher School of Pharmacy, later as professor of medical chemistry at the University of Montpellier, and, later still, as professor of biochemistry and dean of the faculty of medicine at the University of Lille, all in France.
While laboring on problems of fermentation, the break-down of complex molecules into organic compounds via a "ferment" – one need only think of the curdling of milk by bacteria – Bèchamp, at his microscope, far more primitive than Naessens's own instrument, seemed to be able to descry a host of tiny bodies in his fermenting solutions. Even before Bèchamp's time, other researchers had observed, but passed off as unexplainable, what they called "scintillating corpuscles" or "molecular granulations." Bèchamp, who was able to ascribe strong enzymatic (catalytic change-causing) reactions to them, was led to coin a new word to describe them: microzymas (tiny ferments).
Among these ferments' many peculiar characteristics was one showing that, whereas they did not exist in chemically pure calcium carbonate made in a laboratory under artificial conditions, they were abundantly present in natural calcium carbonate, commonly known as chalk. For this reason, the latter could, for instance, easily "invert" cane sugar solutions, while the former could not.
With the collaboration of his son, Joseph, and Alfred Estor, a Montpellier physician and surgeon, Bèchamp went on to study microzymas located in the bodies of animals and came to the startling conclusion that the tiny forms were far more basic to life than cells, long considered to be the basic building blocks of all living matter. Bèchamp thought them to be fundamental elements responsible for the activity of cells, tissues, organs, and indeed whole living organisms, from bacteria to whales, and larks to human beings. He even found them present in life-engendering eggs, where they were responsible for the eggs' further development while themselves undergoing significant changes.
So, nearly a century before Gaston Naessens christened his somatid, his countryman, Bèchamp, had come across organisms that, as Naessens immediately recognized, seem to be "cousins," however many times removed, of his own "tiny bodies."
Most incredible to Bèchamp was the fact that, when an event serious enough to affect the whole of an organism occurred, the microzymas within it began working to disintegrate it totally, while at the same time continuing to survive. As proof of such survival, Bèchamp found these microzymas in soil, swamps, chimney soot, street dust, even in air and water. These basic and apparently eternal elements of which we and all our animal relatives are composed survive the remnants of living cells in our bodies that disappear at our death. So seemingly indestructible were the microzymas that Bèchamp could even find them in limestone dating to the Tertiary, the first part of the Cenozoic Era, a period going back sixty million years, during which mammals began to make their appearance on earth.
And it could be that they are older still, far older. Professor Edouard Boureau, a French paleontologist, writes in his book Terre: Mère de la Vie (Earth: Mother of Life), concerning problems of evolution, that he had studied thin sections of rock, over three billion years old, taken from the heart of the Sahara Desert. These sections contained tiny round coccoid forms, which Boureau placed at the base of the whole of the evolutionary chain, a chain that he considers might possibly have developed in one of three alternative ways. What these tiny coccoid forms could possibly be, Boureau does not actually know, but, from long study, he is sure about the fact they were around that long ago.
When I brought the book to Naessens's attention, he told me, ingenuously and forthrightly: "I'd sure like to have a few samples of moon rocks to section and examine at my microscope. Who knows, we might find somatid forms in them, the same traces of primitive life that exist on earth!"
Over years of careful microscopic observation and laboratory experimentation, Naessens went on to discover that if and when the immune system of an animal or human being becomes weakened or destabilized, the normal three-stage cycle of the somatid goes through thirteen more successive growth stages to make up a total of sixteen separate forms, each evolving into the next. (See diagram of the somatid cycle).
All of these forms have been revealed clearly and in detail by motion pictures, and by stop-frame still photography, at Naessens's microscope. Naessens attributes this weakening, as did Bèchamp, to trauma, brought on by a host of reasons, ranging from exposure to various forms of radiation or chemical pollution to accidents, shocks, depressed psychological states, and many more.
By studying the somatid cycle as revealed in the blood of human beings suffering from various degenerative diseases such as rheumatoid arthritis, multiple sclerosis, lupus, cancer, and, most recently, AIDS, Naessens has been able to associate the development of the forms in the sixteen-stage pathological cycle with all of these diseases. A videocassette showing these new microbiological phenomena is available. Among other things, it shows that when blood is washed to remove all somatids external to the bloods red ceils, then heated, somatids latently present in a liquid state within the red blood cells themselves take concrete form and go on to develop into the sixteen-stage cycle. "This," says Naessens, "is what happens when there is immune system disequilibrium." It is not yet known exactly how or why or from what the somatids take shape. Of the some 140 proteins in red blood cells, many may play a role in the process. The appearance of somatids inside red blood cells is thus an enigma as puzzling as the origin of life itself. I once asked Naessens, "If there were no somatids, would there be no life!" "That's what I believe," he replied.
Even more importantly, Naessens has been able to predict the eventual onset of such diseases long before any clinical signs of them have put in an appearance. In other words, he can "prediagnose" them. And he has come to demonstrate that such afflictions have a common functional principle, or basis, and therefore must not be considered as separate, unrelated phenomena as they have for so long been considered in orthodox medical circles.
Having established the somatid cycle in all its fullness, Naessens was able, in a parallel series of brilliant research steps, to develop a treatment for strengthening the immune system. The product he developed is derived from camphor, a natural substance produced by an East Asian tree of the same name. Unlike many medicinals, it is injected into the body, not intramuscularly or intravenously, but intralymphatically – into the lymph system, via a lymph node, or ganglion, in the groin.
In fact, one of the main reasons the medical fraternity holds the whole of Naessens's approach to be bogus is its assertion that intralymphatic injection is impossible! Yet the fact remains that such injection is not only possible, but simple, for most people to accomplish, once they are properly instructed in how to find the node. While most doctors are never taught this technique in medical school, it is so easy that laypeople have been taught to inject, and even to self-inject, the camphor-derived product within a few hours.
The camphor-derived product is named "714-X" – the 7 and the 14 refer to the seventh letter "G" and the fourteenth letter "N" of the alphabet, the first letters of the inventor's first and last names, and the X refers to the twenty-fourth letter of the alphabet, which denotes the year of Naessens's birth, 1924. When skillfully injected, 714-X has, in over seventy-five percent of cases, restabilized, strengthened, or otherwise enhanced the powers of the immune system, which then goes about its normal business of ridding the body of disease.
Let us for a moment return to the work and revelations of Antoine Bèchamp. As already noted, with the fairly primitive microscopic technology available in Bèchamp's day, it was almost incredible that he was seemingly able to make microbiological discoveries closely paralleling, if not completely matching, those of Naessens nearly a hundred years later. We have already alluded to the fact that the microzymas in traumatized animals did not remain passive, as before, but, on the contrary, became highly active and began to destroy the bodies of their hosts, converting themselves to bacteria and other microbes in order to carry out that function.
While the terminology is not exactly one that Gaston Naessens would use today, the principles of trauma and of destruction of the body are shared in common by the two researchers. Had Bèchamp had access to Naessens's microscope, he, too, might have established the somatid cycle in all the detail worked out by Naessens.
So what happened to Bèchamp and his twentieth-century discoveries made in the middle of the nineteenth century? The sad fact is that, because he was modest and retiring – just like Gaston Naessens- his work was overshadowed by that of his rival. All of Pasteur's biographies make clear that he was, above all, a master of the art of self-promotion. But, odd as it seems, the same biographies do not reveal any hint of his battle with Bèchamp, many of whose findings Pasteur, in fact, plagiarized.
Even more significant is that while Bèchamp, as we have seen, championed the idea that the cause of disease lay within the body, Pasteur, by enouncing his famous "germ theory," held that the cause came from without. In those days, little was known about the functioning of the immune system, but what else can explain, for instance, why some people survived the Black Plague of the Middle Ages, while countless others died like flies? And one may add that Royal Raymond Rife's microscope, like that of Naessens, allowed him to state unequivocally that "germs arc not the cause but the result of disease!" Naessens independently adopted this view as a result of his biological detective work. The opposite view, which won the day in Pasteur's time, has dominated medical philosophy for over a century, and what amounted to the creation of a whole new worldview in the life sciences is still regarded as heretical!
Yet the plain fact is that, based on Naessens's medical philosophy as foreshadowed by Bèchamp and Rife, up to the present time, Naessens's treatment has arrested and reversed the progress of disease in over one thousand cases of cancer (many of them considered terminal), as well as in several dozen cases of AIDS, a disease for which the world medical community sadly states that it has as yet no solution what-so-ever. Suffering patients of each sex, and of ages ranging from the teens to beyond the seventies, have been returned to an optimal feeling of well-being and health.
A layperson having no idea of the scope of Naessens's discoveries, or their full meaning and basic implications, might best be introduced to them through Naessens's explanation to a visiting journalist. "You see," began Naessens, "I've been able to establish a life cycle of forms in the blood that add up to no less than a brand new understanding for the very basis of life. What we're talking about is an entirely new biology, one out of which has fortunately sprung practical applications of benefit to sick people, even before all of its many theoretical aspects have been sorted out." At this point, Naessens threw in a statement that would startle any biologist, particularly a geneticist: "The somatids, one can say, are precursors of DNA. Which means that they some-how supply a `missing link' to an understanding of that remarkable molecule that up to now has been considered as an all but irreducible building block in the life process."*
*Intriguing is a recent discovery by Norwegian microbiologists. On 10 August 1989, as Naessens was preparing for trial, the world's most prestigious scientific journal, Nature (United Kingdom), ran an article entitled "High Abundance of Viruses Found in Aquatic Environments." Authored by Ovind Bergh and colleagues at the University of Bergen, it revealed that, for the first time, in natural unpolluted waters, hitherto considered to have extremely low concentrations of viruses, there exist up to 2.5 trillion strange viral particles for each liter of liquid. Measuring less than 0.2 microns, their size equates to the largest of Naessens's somatids. Much too small for any larger marine organism to ingest, the tiny organisms are upsetting existing theories on how pelagic life systems operate.
In light of Gaston Naessens's theory that his somatids are DNA precursors, it is fascinating that the Norwegian researchers believe that the hordes upon hordes of viruses might account for DNA's being inexplicably dissolved in seawater. Another amazing implication of the high viral abundance is that routine viral infection of aquatic bacteria could be explained by a significant exchange of genetic material. As Evelyn B. Sherr, of the University of Georgia's Marine Institute on Sapelo Island, writes in a sidebar article in the same issue of Nature: "Natural genetic engineering experiments may have been occurring in bacterial populations, perhaps for eons." What connection the aqua-viruses may have with Naessens's somatids is a question that may become answerable when Naessens has the opportunity to observe them at his microscope and compare them with the ones he has already found in vegetal saps and mammalian blood.
If somatids were a "missing link" between the living and the nonliving, then what, I wondered aloud in one of my meetings with Françoise Naessens, would be the difference between them and viruses, a long debate about the animate or inanimate nature of which has been going on for years?
To read more, see: The SOMATID - a Pleomorphic, Ultra-microsopic Subcellular Living and Reproducing Entity
How It Works
The theory behind the work of Gaston Naessens is that cancer is caused by a friendly microorganism (present in all cells) that becomes unfriendly. 714X provides nitrogen to the cancer cells, thus causing this microorganism (somatids – “little bodies”) to cease excreting their toxic compounds and the immune system is mobilized. I presume that at that point the immune system kills the cancer cells. “Furthermore, the 714X therapy unclogs the lymph system, which is responsible for removing toxins from the body.”
Gaston Naessens 714X / 714-X
Before talking about 714X, here is an important quote from an article about 714-X or 714X:
People close to Gaston Naessens' work believe that 714-X is best used early. While they believe it may save one in twelve of the terminally ill patients who turn to it on their death beds, and maybe one in six of the advanced cancer patients who try it as a last hope, when it is given early in the disease process, they feel that it might help almost everyone. Further, anecdotally, even in advanced cancer, 714-X may greatly improve quality of life.
While people with advanced cancer, especially those who the orthodox community has given up on and sent home to die, might clamor for a treatment that has a “one in six” chance of survival, I might respond that there are many alternative treatments for cancer that have a much better survival rate for advanced cancer patients than “one in six.” 714X should probably only be used by people who are not yet “advanced.” (See Case Study #1 in my tutorial for more information on what treatments have excellent results for advanced patients.)
Regarding the theory behind this homeopathic medication, Naessens is one of several well-known alternative health researchers who believes a microorganism is involved with cancer. While some consider this microorganism to be a cause of cancer, others simply consider it to be a symptom of cancer. In any case, the attempt to deal with this microorganism leads to the death of the cancer cell.
714X has been heavily persecuted by the governments of both the U.S. and Canada. Gaston was arrested but eventually found innocent. The FDA has issued an “Import Alert” on this substance (as they have for many other top alternative treatment medicines), meaning Americans must go to Canada, and find a licensed doctor who administers 714X (two of my links below happen to be to clinics that I assume use 714X: Dr. Normal Allen, a chiropractor, and the Centre for Integrated Healing in B.C.).
Supercharging This Treatment
Since this treatment must be administered by a doctor in Canada or Mexico, I will leave it to them to supercharge this treatment.
Site – Comments
- Gaston Naessens – Naessens Home Page (Canada)
- Normal Allan – Good article on Gaston, his microscope, and 714X
- HealthPlusWeb – Some duplication with above article – see Procedure/Protocol
Source: Gaston Naessens' 714X / 714-X Cancer Treatment
714X
What is 714X ?
Developed by the researcher and biologist Gaston Naessens in the 1970s, 714X is categorized as an immuno-modulator health product aiming to both support a weak immune system or to slow down an over-active one. It intends to restore the body's immune defenses without side effects.
714X is manufactured in Canada by the laboratory CERBE Inc. and has been exported to over 80 countries since 1990.
714X is a colorless liquid. Its therapeutic mode of action requires that it is introduced via injection into the lymphatic circulation (first treatment). In some cases, 714X can be introduced via the respiratory track using a nebulizer (secondary treatment).
The story behind the birth of 714X
Gaston Naessens, a biologist born in France but a Canadian citizen since 1975, is the founding father of 714X. He has been working in hematology since 1945 when he finished his studies specialized in Physics, Chemistry and Biology (PCB). For over 66 years, this researcher, who discovered the SOMATID and its cycle in the 1950s, continues to study the role played by this particle in the maintenance of our natural defenses including the immune functions. The somatid, which according to him, is the smallest unit of life, was discovered in fresh blood after numerous and repeated systematic tests where he could establish its evolutionary forms in a 16 phase pleomorphic cycle.
Here is a diagram of the Somatidian cycle as observed under a microscope by Gaston Naessens:
The discovery of the somatid and knowing the existence of its life cycle would have been sufficient to satisfy the intellectual curiosity of a researcher working in fundamental research. However, for Gaston Naessens, there was a step further to take. Knowing that a microscopic observation of blood could reveal the state of one’s immune defenses was not sufficient. Knowing that the disease was inevitable and nothing was done to prevent it did not correspond to his code of ethics. This extra step was thus the search for natural ways that could restore the functions of our defense system without causing any harm to all the blood’s elements. This work, which began in the 1950s, continues today and is embodied in the design of many health products intended to act on the Somatidian cycle . It was in the 1970s, following several experiences with other health products he had made available to the European public in the 1950s and 1960s, that he created a new product: 714 X . (non-toxicity confirmed in 1978).
714X is a non-toxic natural health product capable of restoring the biological terrain when the immune defense function is too weak or too active.
Despite the obstacles and resistance to his new ideas, Gaston Naessens continues to move forward, and his perseverance has earned him at least the satisfaction of collaborating, as an independent researcher, towards the emergence of a new paradigm in health and to offer humanity effective and non toxic health products.
How does this product work ?
714X works in two ways:
- In liquefying the lymph, 714X promotes cleansing for a better disposal of metabolic waste circulating in the blood (toxins).
- Once 714X has been absorbed through the lymph, it brings to the blood circulation particular elements (structured and organized molecules including nitrogen fixed to camphor) to directly address white blood cells (leucocytes) to resume their respective defense functions. They may then restore previously disrupted intercellular and intracellular communication.
Thus, the inflammatory process, common to many degenerative diseases, fades and comes back to its normal state. Cell, tissue and organ repairprogress at a rate specific to each individual.
How to administer 714X ?
Usage protocol
714X is a unique product due to its mode of intromission. In addition to this, 714X normalizes the biological terrain using the lymphatic circulation as a gateway into the body.
The particular choice for the mode of intromission of the product is based on the belief of its designer, who is convinced that the lymphatic system is the main highway system, one that facilitates the elimination of metabolic toxins circulating in the blood and that brings to the cells essential elements for their optimal functioning.
Choosing the lymphatic circulation as a mode of entry has practical unavoidable consequences as it becomes necessary to deal with anatomic realities. Nature has endowed the human body with a double lymphatic circulation. A large and a small circulation, each with their drainage area, that flow into the bloodstream.
Lymphatic circulations' drainage zones
To access the large lymphatic circulation which drains 75% of the body surface, the mode of intromission is the perinodularl injection (around the lymph nodes) in the right inguinal region (the groin).
Basic treatment with 714X requires a box containing two vials of 6.5 ml of product. This quantity allows 21 days of injections to constitute a cycle.
To access the small lymphatic circulation, the preferred method is the introduction of the product by inhalation with the use of an ultrasonic nebulizer that allows the absorption of the product via the small glands that line the respiratory tract (714X divided into particles smaller than 5 microns).
714X's secondary treatment (the nebuliser method) must be performed in addition to the perinodular injection. It requires 3 boxes of 7 ampoules of 2 ml for 21 days of treatment which constitute 1 cycle.
The perinodular injection
Self-injection, even when one has already decided to use 714X is an unfamiliar process. The word injection itself raises some apprehension.
At the beginning of the treatment, it is completely understandable to be hesitant and to worry about self-injecting in the right area.
The location of the injection site is the first and most critical step.
714X users’ feedback allow us to say that the injection technique, when properly mastered the first 5 days, can be considered an enjoyable daily activity which can be incorporated in your daily schedule as a relaxing time. This activity then becomes a simple daily gesture which can be paired with listening to pleasant music in a relaxing and comfortable setting.
Finding the injection site
- With the right hand (for right-handed people) more precisely with the middle and ring finger, feel around the fold of the right groin area until you find the spot where a cardiac pulse is felt. This is the femoral artery pulse. For some, this pulse is found deep, for others, it is more superficial. Some have a pulse above or below on the fold line of the groin. Depending on the anatomy of each person, finding the pulse could take longer for the first few times. It should be easier to locate the following times.
- Once the femoral artery pulse is found and to facilitate locating the precise injection site, trace an imaginary line between the femoral artery pulse and the navel..
For children weighing less than 30 kg (66 pounds), the injection site is located on this imaginary line, 1 to 2.5 cms (0.5 to 1 inch) above the femoral artery pulse.
By putting pressure on the femoral artery where the pulse is felt, the three deep lymph nodes are brought up to the surface. The product injected into the periphery of these deep lymph nodes will be absorbed by one of these nodes, hence the term: perinodular injection. The optimal injection zone has a surface area comparable to a small disc measuring 2 cm. Day after day, the needle does not have to be inserted in exactly the same spot, but in the same area, leaving some room for maneuver.
Two important points to remember concerning finding the injection site:
- Introducing the product on the right side of the body is proposed because the lymphatic route flows from right to left. By introducing the product on the right we ensure the best possible drainage of the large lymphatic circulation.
- If during the first few attempts, you still have a doubt about the exact location of the injection site, there is nothing wrong with restarting the process (so long as you ensure that the injection zone is re-sterilised according to the protocol).
Please refer to the 5_steps_perinodular_injection.pdf for the five steps of the perinodular injection.
Compatibility of 714x with other treatments
714X is a health product which is introduced into the lymphatic circulation. This is one of the characteristics that makes 714X unique.
Consequently, this product never comes in contact with ingested food or any part of the digestive system. 714X has no direct interference with food, natural health products or prescribed medications.
714X is considered as a product of Universal Health totally compatible with pharmacological products as well as natural health products, because it is through the lymph that 714X flows into the bloodstream to act on white blood cells (leukocytes), and on the cellular environment. 714X acts on the biological terrain.
In part due to its specific action on white blood cells’ (leukocytes) cytokine receptors, 714X not only acts on immune defense but it also supports the expected positive effects of other healthcare products taken orally. 714X works with all other products introduced externally.
In the event that a patient must temporarily receive certain conventional treatments or a surgical intervention, 714X taken simultaneously can be beneficial as it acts as reinforcement to invalidate their unavoidable side effects by supporting the vital energy and the natural defenses.
714X is not only universally compatible with all products, but it offers as well the benefit of invalidating the adverse side effects of other products, while supporting the vital energy.
In oncology, and considering that cancer is a huge public health concern, 714X becomes a helpful support to go through the intense periods of targeted treatments (surgery, chemotherapy, radiation, etc..), as well as during recovery periods and therapeutic breaks.
Since it is non-toxic, 714X can be used preventively in healthy people. Immune resistance is further increased to accommodate the many challenges of personal and / or professional life.
With non conventional treatments
Because it supports the body's natural defenses, 714X can be taken simultaneously with most natural health products.
The only exception to this statement remains anti-angiogenic products of natural or synthetic source (eg, shark or bovine cartilage).
This is not to say that these products are not effective, but their mode of action is not complementary with 714X.
The reason for this incompatibility is as follows:
The effect of anti-angiogenic products of any kind (used for cancer treatment in the model which focuses on the elimination of the tumor) is to create oxygen deprivation by cutting the blood flow that feeds the tumor. The intended effect is to reduce the growth of the tumor by depriving it of nutrients.
714X needs to go through the blood circulation near the tumor so that the tumor necrosis factor secreted by the reactivated white blood cells can act on the tumor and reduce it.
The secretion of the tumor necrosis factor is the white blood cells defense mode of activity by which all of their secretions, released into the blood, react and shrink the tumor, regardless of its location in the body.
With certain conventional treatments
This section has dealt with how 714X is compatible with different health products that go through the digestive system.
In the case of therapeutic approaches in particular medical interventions (as for the case of cancer for example) 714X can be taken simultaneously with conventional care. As it acts on the natural defenses of immunity, 714X is complementary to conventional treatments and will not counteract them. On the contrary, 714X can reduce, and even eliminate much of the undesirable side effects usually associated with conventional treatments, thus permitting a better quality of life.
Moreover, as 714X acts on the lymphatic circulation, taking a cycle of 714X before surgery will minimize the risk of uncontrolled spread of anarchical cells elsewhere in the body as these can be drawn into the lymphatic system (not only in the case of cancer).
714X taken before surgery will provide better cell, tissue and organ repair after surgery (wound healing).
Statistics and data use
In everyday language, the notion of "statistics" in health often involves the estimated success rate of a specific product against a particular pathology.
For 714X, we are often asked the following question: "Do you have statistics on your cancer product? "This approach is very legitimate from the point of view of the consumers who are accustomed to medication that acts on the disease.
This expectation of the consumer, regarding the effectiveness of the product 714X against his own illness, is based on the conventional approach. This is the usual way of doing things in conventional medicine and it is always an external product that comes in to correct the symptoms of the disease.
In natural medicine, a product acts upon the biological terrain. This is a different view. In the biomedical model, the predictive ability of the effects of a chemical product is made possible because the product has been studied and measured in a laboratory (often on mice), based on the toxicity of the molecule. The final product is designed to achieve measurable benefits that will outweigh the inevitable incurred risks.
It is different for 714X as it is non-toxic. In the holistic model of health, also known as global health model, all the elements of the context of one’s life are very important. Since the natural products that are offered are non-toxic, they aim to improve natural health factors in order to support the biological terrain, rather than acting locally to neutralize symptoms of a local physiological disorder
This is why within this global health model to which 714X pertains to due to its non-toxic nature, it becomes impossible to make mathematical predictions on the absolute effectiveness of the product, because it is the uniqueness of each one of us that will determine the speed and extent of efficacy of the product in its context.
In short, for 714X, as for any natural health products (eg vitamin C) or special treatments (eg massage), the ultimate impact will always depend on the biological terrain unique to each individual and life context in which each person evolves.
The perception of the impact of 714X, as a health treatment, is usually shown through individual observations felt and manifests through quality of life criteria such as one’s vitality, sleep, appetite, etc.
Although it acts in all cases on the lymph and the white blood cells (leukocytes), it is not possible to attribute a predictive character to 714X because it integrates itself to the biological terrain of each individual, with their own uniqueness. The physiologic effects are measureable little by little as the cleansing and body repair progress, according to each individual biological terrain.
Clinical experience from the last thirty years (22 years of use under the authority of a governmental regulatory agency) means that 714X is a product that has surpassed the « test of time ». We can say with complete confidence that its utilization brings after the first 21 days of use a better quality of life. This is expressed in many ways according to each individual and depending on the evolution of the disease, the care that was given and each person's experiences.
In general, the effects of 714X under the parameters of conventional blood tests are usually measurable after a minimum of 3 cycles of use.
Scientific data on 714X
714X is the invented name of Triméthylaminohydroxybicycloheptane chloride.
Chemical formula
Chemical composition
714X is an isotonic solution at physiological pH (7) containing nitrogen as the main active ingredient, camphor as a vehicle, or a nitrogenated derivative of camphor, at a level of 0.09 mg/ml (complying with the pharmaceutical industry’s norms of injectable solutions), mineral salts, and 18 different trace elements (metallic elements), measured in parts per million, and magnesium at a level of 6.5 ppm. these trace elements, even in trace amounts, do have a biological significance.
The level of sodium chloride (NaCl) is estimated at 8.2g/litre.
A plasma emission spectrometry study identifies the 18 following elements measured by the following parts per million):
Aluminum < 0.5 ppm Calcium 0.5 ppm Mercury < 1.0 ppm
Antimoine < 1.0 ppm Chrome < 0.1 ppm Molybdenum < 1.0 ppm
Arsenic < 1.0 ppm Cobalt < 1.0 ppm Nickel < 0.1 ppm
Baryum 0.7 ppm Cuivre 0.01 ppm Phosphore < 5.0 ppm
Bore < 0.05 ppm Fer < 0.1 ppm Plomb < 1.0 ppm
Cadmium < 0.05 ppm Magnésium 6.5 ppm Zinc 2.0 ppm
Conclusion
The absence of proteins and immunoglobulins shows that this is not an immune serum prepared after injection to animals. 714X is not a vaccine. There is no risk of allergies or anaphylactic shock.
The presence of sodium chloride at a level of 8.2 g / liter shows that this is an isotonic solution with a pH of 7 (physiological solution). This solution complies with norms for injectable solutions of the pharmaceutical industry.
A mass spectrometry coupled with a chromatography reveals the presence of camphor or trimethyl-1.7.7 bicyclo (2.2.1.) heptanone-2 whose concentration we measured as 0.09 mg / ml (90 ppm). A nitrogenated compound and hydrochloric acid were also identified.
The comparative study using camphoroxime shows that this molecule does not exist as such in the analyzed sample of 714X. The precise nature of the nitrogenated compound contained in 714X could not be clearly identified.
Eighteen metals (metallic elements) were measured. They were all found at trace levels (parts per million) and considered to be of no biological significance, except for magnesium which at 6.5 ppm was too low to be given a therapeutic property. (This is the opinion of the private laboratory. However, the manufacturer claims that these trace elements, even in trace amounts, do have a biological significance)
Summary of the chemical analysis
Ultimately, 714X is an isotonic solution at physiological pH (7) containing camphor or a nitrogenated derivative of camphor, at a level of 0.09 mg/ml, complying with the pharmaceutical industry’s norms of injectable solutions.
Therapeutic class
714X belongs to a health products category that acts upon natural defenses including the immune function.
Depending on the circumstances, 714X acts on a severely weakened immune system (by strengthening it) or on an overactive immune system (by slowing it down). For this reason, 714X is recognized as an immuno modulator.
Moreover, to date, 3 patents confirm that 714X is an immunomodulator.
Canadian Patent: 2010.CA02297998
European Patent: 2005.EP1251841-B1
American Patent: 2003-6-596-295
Research Report – Immunologic test applied to 714X
(vitro Effects of 714X on mononuclear cells of peripheral blood)
Sponsor:
Diane Van Alstyne, Ph.D.
Inventors Ink
#23-130 MacPherson Ave.
Toronto, Ontario, CANADA M5R 1W8
Period of Experimentation:
March 1999, Boston, Massachusetts, USA
Results and conclusions
Peripheral blood mononuclear cells and monocytes exposed to 714X in vitro show the following effects:
- Over 50% activation and / or cell differentiation, resulting in morphological changes and modification of cell adherance on microwell plates.
- An atypical and immediate intracellular accumulation of Ca+2 ions in monocytes, and none in the control sample.
- Induction of cytokines, including tumor necrosis factor alpha (TNF-α), interleukin-1β, -6, 8, and an increase in the intracellular level of cytokine-specific mRNAs including 362 bp for TNF-α, 330 bp for IL-1β, 496 bp for IL-6, and 407 bp for IL-8. Structural analysis of molecular components contained in 714X (compared to the inactive control product) reveals the presence of two nitrogen-containing compounds derived from camphor, molecular weight of 169.5 and 151.25, unique to 714X
Based on the foregoing data, the sponsor suggests that 714X contains at least one component which acts as a substance that promotes the induction of cytokine in vitro and has the following characteristics:
- Ability to bind to receptors to initiate activity;
- Possession of a cell affinity, and
- Possession of intrinsic activity.
TNF-α, IL-1β, IL-6 and IL-8). These data provide scientific evidence to 714X’s immunomodulatory role.
It is believed that the 714X enhances the immune response and plays a role in the removal of the tumor cell. The results appear to support this theory by suggesting that induction of proinflammatory cytokines represent at least one mechanism responsible for anti-tumor activity in vivo of 714X.
Assurance of Quality Control:
Data reviewed and report provided by researcher Diane Van Alstyne, Ph.D.
Report published 25 August 2000
To read more, see: 714X | Cerbe Distribution Inc
Manufacturing
https://www.cerbe.com/sites/default/files/videos/production_en.mp4 (video showing the manufacturing process of the 714X product.)
The complete manufacturing process is comprised of four steps:
At each of these steps, the strictest aseptic norms and standards are adhered to, ensuring the product is safe and secure. CERBE, the manufacturer, guarantees the sterility of its products as all of its manufactured products are sterilized after bottling using traditional autoclave sterilization procedures.
CERBE voluntarily adheres to good manufacturing practice (GMP)
Once these four steps are complete, CERBE Inc. can assure its clients and consumers of the delivery of a natural health product that is sterile, safe and ready to use in Canada in collaboration with the Special Access Program of Health Canada or for exportation abroad.
The manufacturing process
The bottling process
The sterilization process
Labelling
The manufacturing process
The mix of unique base products The products of CERBE Inc. are innovative products, unique and specifically developed to act on the immune system without negative side effects. The first step is therefore the mix of its base products following a new and unique process of arranging molecules. The innovative nature of Gaston Naessens’ manufacturing process is confirmed by the attainment of the following patents:
The bottling process
This step is performed in a sterile lab, in an enclosed space especially built and designed for this stage of the manufacturing process, with ultra-specialized and modern equipment specifically designed for the manufacturing needs of CERBE Inc. The best practices of the laboratory are applied in order to maintain the highest quality standards in manufacturing in the natural health products industry.
The sterilization process
This step is crucial to ensure the safety of products, injectable or otherwise. All of the products manufactured by CERBE Inc. are mandatorily sterilized using traditional autoclave sterilization procedures. This means that all products are sterilized at 212 degrees centigrade under 18 lbs of pressure for a minimum period of 20 minutes. This self-imposed requirement of CERBE Inc. necessitates the use of specialized bottles able to support extreme high temperatures. None of CERBE Inc.’s products are bottled in plastic containers.
Labelling
Once the bottling and sterilization processes are completed, the labeling is done in a completely different laboratory specially designed for this step. Once again, a final quality assurance check is done, one bottle at a time, under ultra-violet lighting, before finally placing specific regulatory standard labels for each of the products. For each product, the identification number, expiration date, and the specification of bottles for exportation are clearly marked on each commercial label.
Source with video embedded: Manufacturing | Cerbe Distribution Inc
Gaston Naessens & The Somatid
September 9, 2016
Gaston Naessens was treated badly by the world for creating his ingenious invention he called a Somatoscope. Today, these devices are called phase contrasting microscopes that do live cell blood exams. The medical mafia has been doing its best to keep practitioners, who use these incredible devices, out of the free market; because of what they reveal that can get a patient well. However, as the battle rages on in the free market place, more and more the western medical system is failing to keep these devices from emerging. In truth, every western doctor on the planet should be using these incredible microscopes to help get their patients well. Look below and learn more!
Still alive at age 92, Gaston Naessens was born March 16, 1924, in Roubaix, in northern France, near the provincial capital of Lille, the youngest child of a banker who died when his son was only eleven years old. In very early childhood, Gaston was already showing precocity as an inventor. At the age of five, he built a little moving automobile-type vehicle out of a “Mechano” set and powered it with a spring from an old alarm clock.
Continuing to exhibit unusual manual dexterity, a few years later Gaston constructed his own home-built motorcycle, then went on to fashion a mini-airplane; large enough to carry him aloft. It never flew, for his mother worried he would come to grief, and secretly burned it on the eve of its destined takeoff.
After graduation from the College Universitaire de Marcen Baroeul, a leading prep school, Gaston began an intensive course in physics, chemistry and biology at University of Lille. When France was attacked and occupied by Nazi forces during Word War II, young Gaston, together with other fellow students was evacuated to southern France. In exile near Nice, he had the highly unusual opportunity to receive the equivalent of a full university education at the hands of professors also displaced from Lille.
By the war’s end, Naessens had been awarded a rare diploma from the Union Nationale Scientifique Francaise, the quasi-offical institution under whose roof the displaced students pursued their intensive curriculum. Unfortunately, in an oversight that has cost him dearly over the years, Naessens did not bother to seek an “equivalence” from the new republican government set up by General Charles de Gaulle. He thus, ever since, has been accused of never having received an academic diploma of any kind.
Inspired by his teachers, and of singular innovative bent, Gaston, eschewing further formal education– “bagage universitaire” (academic baggage) as he calls it — set forth on his own to develop his microscope and begig his research into the nature of disease. In this determination, he was blessed by having what in French is called jeunesse dorfee, or gilded childhood — “born with a silver spoon in his mouth,” as the English equivalent has it. His mother afforded him all that was needed to equip his own postwar laboratory at the parental home.
— Taken from the book titled “Suppressed Inventions” written by Johnathan Eisen (Page 157 of 560)
What now follows are two videos that reveal Gaston Naessens Somatoscope, how it works and how it was instrumental in revealing the 16 stage cycle of the somatid ability to pleomorphosize.
Source: Gaston Naessens & The Somatid - KFFMenterprises
Gaston Naessens and 714X
By Dr. Gaston Naessens and Jacinte Levesque Naessens
Image courtesy of Cerbe Distribution, Inc.
A diagram of the Somatidian cycle as observed under a microscope by Gaston Naessens.
Gaston Naessens, a French-born researcher based in Sherbrooke, Québec, who has been at work since the early 50s, is a true pioneer in the field of live blood observations.
Through the optical performance of his unique light microscope (the somatoscope), Gaston Naessens discovered the smallest unit of life: the somatid.
He was able to understand the life cycle of the somatids through their different evolutive forms. This led him to a further observation of an “inner biological protection gate” that reveals the state of the immune system.
This inner protective gate, also a witness of the natural defenses, can be altered by a combination of external and/or internal factor. If the “inner gate” is being over-challenged, it breaks down the homoeostasis of blood that can thereafter lead to various types of degenerative disorders (including cancer), initiating with inflammation, the common precursor of all degenerative diseases.
Naessens was able to monitor the state of the immune system from an innovative perspective: the visual observation of live blood through his specific assessment of the somatidian cycle.
Immunotherapy, the fourth arm of cancerology (after surgery, chemotherapy and radiology), was declared a major scientific breakthrough in 2014. Naessens’ vision of cancer linked to the immune system is thus proving to be a sound innovative way to address disease from an epigenetic perspective.
As early as 1961, Naessens proposed a therapeutic agent / therapy capable of addressing the immune system as it was in its evolution with cancer. This was then considered heretic. Today, it fits perfectly with the scientific revolution that encompasses wider factors rather than the strict genetic components of degenerative diseases.
Naessens’ knowledge and understanding of the somatidian cycle as a witness of the evolution of the disease, allowed him to create a restorative product for the immune system. 714X is a nontoxic health product capable of restoring the normality of the somatidian cycle, consequently restoring the inner balance.
714X has been granted four patents testifying of its uniqueness, confirmed by various juridictions. (Patents obtained: 2003 USA, 2005 EC, 2010 Canada, 2014 Japan.)
It is important to recall that 714X, a proprietary blend, is a true immune modulator that can be either used for curative purposes, alone or in combination with conventional modalities, or simply used alone as a preventative agent.
Naessens’ vision of health is highly compatible with the holistic approach where many factors impact the biological system including the emotional, the intellectual and the spiritual factors. It is thus essential to address each person as the unique expression of a biological signature.
A trustful partnership between consumers and their health care providers (conventional and/or alternative) is the new trend that Naessens supports entirely, bringing integrative medicine to the forefront of a new era.
Gaston Naessens, at 92 years old, is still young at heart and continues to work at his own pace, in peace, always eager to find nontoxic solutions to maintain optimal health.
For more information on Naessens work or on the 714X product visit the Cerbe Distribution, Inc. web site.
See also Change of Strategy in Cancer Care Management: Cancer Immunotherapy a Major Breakthrough Leading to a Paradigm Shift by Dr. Gaston Naessens and Jacinte Levesque Naessens, originally published in Wise Journal, Fall 2015.
Source: Gaston Naessens and 714X | Foundation for Alternative and Integrative Medicine
The Amazing Wonders of
Gaston Naessens
February - March 1994
The landscape of medical science is on the verge of being radically altered forever by the use of a powerful microscope (the Somatoscope) developed by Gaston Naessens of Quebec, Canada, This incredible device reaches magnification levels of 20,000 to 30,000 diameters—well above the 2,500 diameter limit of conventional microscopes. The sheer magnitude of the difference in performance gives the appearance of either a gross violation of the laws of physics, or fraud.
Its radical departure in performance from optical and scanning electron microscopes registers this as a truly great discovery. Unfortunately, in most fields of science, a great deal of effort is put forth into listing why something will not work instead of attempting to duplicate the results. This in turn creates a situation where what was science, turns into religion where the orthodox dogma is to be taken on faith, and that which defies dogma is to be persecuted as heresy.
Establishment of a dogma slows down the rate new discoveries can be made. In the medical fields, slow acceptance of new ideas can cause many needless deaths. This is the case with the supermicroscope and the discoveries of B&hamp, Rife and Naessens.
Read more at: The Amazing Wonders of Gaston Naessens by Steven R. Elswick
Dr. Gaston Naessens
Gaston Naessens, ND.
Gaston Naessens, ND is the president, founder, and CEO of Cerbe Distribution, Inc., a private laboratory in Québec, Canada specializing in fundamental research in biology, including hematology.
Cerbe is also the manufacturer of Triméthylaminohydroxybicycloheptane chloride (714X) for which four patents have been granted [2003 (USA), 2005 (Europe), 2010 (Canada) and 2014 (Japan)].
He is a biologist researcher engineer and developed a revolutionary microscope, called the somatoscope, capable of observing unstained living matter. The somatoscope enabled him to discover a new particle in human blood, he calls the somatid. From this, he developed the Somatidian theory and developed new responses to diseases affecting the immune system.
Source: Dr. Gaston Naessens | Foundation for Alternative and Integrative Medicine
Source websites:
Cerbe Distribution Inc | A Trustworthy Partner for Better Health
Gaston Naessens & 714X
Dr. Gaston Naessens | Foundation for Alternative and Integrative Medicine
Gaston Naessens and Somatid biology
Book on Gaston Naessens: The Persecution and Trial of Gaston Naessens by Christopher Bird
Gaston Naessens and Somatid biology
The landscape of medical science is on the verge of being radically altered forever by the use of a powerful microscope (the Somatoscope) developed by Gaston Naessens of Quebec, Canada. This incredible device reaches magnification levels of 20,000 to 30,000 diameters — well above the 2,500 diameter limit of conventional microscopes. The sheer magnitude of the difference in performance gives the appearance of either a gross violation of the laws of physics, or fraud.
Its radical departure in performance from optical and scanning electron microscopes registers this as a truly great discovery. Unfortunately, in most fields of science, a great deal of effort is put forth into listing why something will not work instead of attempting to duplicate the results. This in turn creates a situation where what was science turns into religion where the orthodox dogma is to be taken on faith, and that which defies dogma is to be persecute as heresy.
Establishment of a dogma slows down the rate at which new discoveries can be made. In the medical fields, slow acceptance of new ideas can cause many needless deaths. This is the case with the super-microscope and the discoveries of Bechamp, Rife, and Naessens.
HISTORICAL NOTES
In the 1930s, an obscure and dedicated scientist, Royal Raymond Rife, had successfully developed the Universal Microscope which was able to provide amplification levels of 60,000 times without killing the specimens! Rife was able to observe live viruses and their reaction to certain stimuli. His observation that bacteria could change into viruses and viruses could change form violated the strongest medical dogma — the germ theory of disease.
By 1934, after learning how to seek out and destroy the insidious cancer virus, Rife opened a clinic in which he cured 16 out of 16 patients within 3 months! Working side by side with some of the most respected researchers in America, Rife treated patients electronically to kill the virus and then allowed the body's immune system to restore the body to full health. Many prestigious ( and competent ) organizations and institutions oversaw and verified much of Rife's work during the 1930s.
Independent physicians using Rife's therapy were treating and curing as many as 40 patients per day. Other degenerative conditions and illnesses such as cataracts, herpes and tuberculosis were found to be reversible and curable with Rife's equipment. This work was described in various medical journals of the time as well as the Smithsonian Institution's annual report and Science Magazine. Unfortunately, Rife's success attracted the attention and wrath of the American Medical Association (AMA) and the powerful pharmaceutical companies - the organised opposition of the medical fields.
Although Rife's work was in direct conflict with the orthodox views of his time, he was supported by many top-rated doctors. Many of these doctors continued using these devices in secret in defiance of the AMA and the US government. The carefully documented records kept by these brave doctors and testimonials by their patients vindicate Rife's theories. Many of these case histories and anecdotes about Rife's treatment can be found in the book "The Cancer Cure That Worked" by Barry Lynes.
The fascinating work of Rife was suppressed and he — like Nikola Tesla before him — joined the ranks of the forgotten inventors of the early part of this century. It has only been in the past few years that the general public has begun to develop an awareness that there is something wrong in the technical world.
THE MODERN UNIVERSAL MICROSCOPE
What Rife accomplished optically in the 1930s with his Universal Microscope, Gaston Naessens accomplished with a combination of optics and electronics in the 1940s in his Somatoscope. Born on 16 March 1924 in Roubaix, France, Gaston displayed a predisposition to be an inventor when at the age of five he built a little moving auto-like toy from a Meccano set and powered it with an alarm clock spring. Later, he built a home-made motorcycle and a mini-airplane!
While attending the University of Lille, Gaston nearly had his education disrupted by the German invasion. Fortunately, Gaston and his fellow students escaped to Nice where they carried on their education in exile. He was awarded a diploma from the Union Nationale Scientifique Francaise — a quasi-official institution under whose auspices the education of the displaced students continued. He did not bother seeking an equivalency degree from the de Gaulle government when French rule was restored.
At the young age of twenty-one, frustrated by the limitations of conventional microscopes, Gaston set out to build a superior microscope. Technical assistance was provided by German craftsmen from Wetzlar, Germany, who checked out many of Gaston's ideas on optics. Privately, Gaston devised the electrical manipulation of the light source. Once the technical aspects were resolved, Gaston had the body of his microscope constructed by Barbier-Bernard et Turenne, technical specialists and defence contractors near Paris.
THEORY OF OPERATION
The Somatoscope mixes light from two orthogonal light sources — a mercury lamp and a halogen lamp. The light from both sources enters a glass tube at 90 degrees from each other. As the light waves beat against each other, a strong carrier wave of light emerges and travels down the light tube. ( It should be noted that two electromagnetic fields superimposed on each other at 90 degrees is a classic scalar formation! ) As the light travels down the tube, it passes through a monochromatic filter which forms it into a monochromatic ray. The ray is then passed through a large coil that surrounds the tube. The coil's magnetic field divides the ray into numerous parallel rays that are then passed through a Kerr cell which increases the frequency of the ray before being injected onto the specimen.
The light, which contains the carrier and a mixture of selected signals in the UV range, stimulates the biological material in the Somatoscope to the point that the specimens give off their own light. (Rife referred to this as luminescence.) This is the key to the ultra-high resolution that has been achieved by Gaston Naessens.
Conventional microscopes pass light through the specimen which theoretically limits the resolution of optical microscopes to the wavelength of light. The finest optical microscopes have achieved magnification levels of 2,500 diameters. At levels above this, the resolution is limited by the wavelength of light and further magnification merely creates a blur! Higher resolutions have been achieved by microscopes that do not use lenses, but instead use apertures which are smaller than the wavelength of light. One such microscope engineered at Cornell University has achieved a resolution of 400 angstroms — a far cry from the 150 angstroms achieved by Naessen's Somatoscope.
The Somatoscope does not attempt to illuminate the specimen by passing light through two small objects. Instead, the illumination source is actually stimulating the specimen to the point where it generates its own light. The light itself expands as it moves outward and because the specimen itself is generating the light, the physical restrictions encountered by regular optical microscopes no longer apply. By converting the specimen into a light source, Gaston Naessens has converted the magnification problem from one of resolution to that of light detection! At magnification levels above 5,000 diameters, light levels drop off to the point that film is necessary, but the resolution is there.
To further research along the lines he has pioneered, Gaston has developed junior models of his Somatoscope for field use. These field units allow researchers to obtain illumination and stimulation of the specimens of the larger unit. The field units are capable of magnifying 6,000 – 7,000 diameters, although routine work will usually be at 3,500 – 4,000 diameters. The lower light levels of the higher magnification requires that a lower level of magnification be accepted for field use in order to maintain portability in the smaller units. One such unit will be in use in Colorado Springs at Clifford and Associates.
The Somatoscope has enabled researchers to discover the importance of colour and its relationship to the material being observed. The wavelengths of light generated are related to the size of the object and the health of the cell. For instance, the red blood cells vary from yellow/green to orange (540 nm to 580 nm) and white blood cells are rich in blue/violet (490 nm to 510 nm). Exposure to toxic materials, even in minute amounts, causes significant shifts in colour. Even 'safe' amounts of toxic materials like mercury and the aluminium in toothpaste cause significant degradation to red blood cells as I was able to witness from specimens on a videotape produced from the Somatoscope.
THE SOMATID CYCLE
In a long lost chapter in the history of science, a violent controversy took place in France between the illustrious Louis Pasteur and Antoine Bechamp, a noted professor of physics, toxicology, medical chemistry, and biochemistry. Bechamp's work led him to discover "microzymas" (tiny ferments), which were characterised by a host of small bodies in his fermenting solutions.
After years of study, Bechamp came to the conclusion that these microzymas were more basic to life than cells. Even with his crude equipment, he was able to observe that the microzymas underwent dramatic transformations during their life cycle. This caused Bechamp to champion the idea that the cause for disease lay within the body. Pasteur's germ theory held that the cause came from without. Pasteur's outspokenness helped the germ theory win out and it has dominated medical thinking for the past century.
Now, a hundred years later, Gaston Naessens has discovered an ultra-microscopic, subcellular, living and reproducing microscopic form which he christened a "somatid" (tiny body). This new particle could be cultured outside the bodies of the host. Naessens also observed that the particle had a pleomorphic (form-changing) life cycle, which has sixteen stages. Only the first three stages of the somatid's life cycle are normal.
Naessens discovered that when the immune system is weakened or disrupted, the somatids go through the other thirteen stages. The weakening of the immune system could be brought about by a number of causes, such as exposure to chemical pollution, ionising radiation, electric fields, poor nutrition, accidents, shock, depression, and many more.
Incredibly, Naessens' research has resulted in the association of degenerative diseases (rheumatoid arthritis. multiple sclerosis, lupus, cancer and Aids) with the development of various forms in the sixteen-stage pathological cycle. The ability to associate the disease with specific stages has enabled Naessens to 'prediagnose' conditions in advance of when they would clinically appear.
This discovery puts Gaston Naessens at odds with the orthodox medical philosophy of today which has embraced Pasteur's germ theory wholeheartedly. Naessen's work is repeatable. The ability to culture somatids is a bell-wether to the rewriting of micro-biology!
Naessens has stated:
"I've been able to establish a life cycle of forms in the blood that add up to no less than a brand new understanding of the basis of life. What we're talking about is an entirely new biology, one out of which has fortunately sprung practical applications of benefit to sick people, even before all of its many theoretical aspects have been sorted out."
714X
The research of Gaston Naessens has culminated in the discovery of 714X — an enzyme which helps the immune system do its job. 714X is a derivative of camphor and is injected interlymphatically — a process that the medical fraternity holds to be impossible. Yet the fact remains that many people have learned how to administer the medication through the lymph nodes.
When properly administered, 714X stabilises and strengthens the immune system in most cases. This allows the immune system to go about its normal business in ridding the body of disease. In other words, cancer is treated like an infection, not a state of cells.
Like Bechamp and Rife before him, Gaston states unequivocally that "germs are not the cause, but the result, of disease."
714X will not help everyone — especially where there has already been extensive use of chemotherapy and radiation. Chemotherapy and radiotherapy wipe out the immune system and other bodily resources.
THE SECOND CHANCE
The cancer death toll between 1970 and 1986 ( in the U.S.? ) was approximately 6 million. Sadly, the conventional treatments of chemotherapy and radiation are nothing more than slow death sentences that enrich the cancer industry. Possible miracle cures are quickly quashed by the FDA (Food and Drug Administration) and the various medical societies around the world. It is a sad commentary that in a country that prides itself on freedom, terminally ill patients cannot make an informed decision to participate in experimental treatments that may save their lives.
714X is available in the United States. "Writers and Research" is one organisation working closely with the FDA and the IRN ( Institution Review Board ) to do work with 714X legally and ethically. 714X is an injected medication and must be prescribed by a doctor.
For a list of doctors prescribing 714X or an information packet, contact:
WRITERS AND RESEARCH
4810 St Paul Boulevard
Rochester, NY 14617 USA
Phone: 1–800–448–4332
Source: Gaston Naessens and Somatid biology
The Story of Gaston Naessens Featured in Canada’s Saturday Night Magazine
In it’s December issue, Canada’s popular magazine, Saturday Night, featured the trials and victories of eminent biologist Gaston Naessens. The well-written 12 page article chronicled the life of Naessens from the discovery of the somatid cycle (see Figure 1) to the development of the formula 714-X, to the trials and persecution he faced and continues to face. Below is a historical summation of the article:
Late 1940’s – From the work of individuals such as Béchamp and Emile Doyen, Naessens began work on what would become the somatoscope. What would later be termed dark-field microscopy (but not as sophisticated), Naessens’ instrument allowed him to examine live blood at extreme magnifications as well as with exceptionally high resolution. One improvement with this instrument is its ability to see particle via light refraction as opposed to traditional staining methods.
Mid 1950’s — Moved lab to Paris from Lyon, France. Opposition began to mount from the traditional medical authorities due to innovative theories and treatments, not to mention successes.
Early 1960’s — Naessens treated over 10,000 individuals afflicted with various illnesses, many life-threatening, with extraordinary results. On the other side, he was twice brought before the “bar” (medical authorities). He was fined heavily and forced to close his Paris lab. Much of his equipment was confiscated.
1962 — Naessens tried again to start his laboratory on the island of Corsica, but Corsica was still France. Patients continued to seek him out, as did the authorities.
1964 — Naessens pursued his work in Canada, leaving Corsica with only a few key components of his microscope.
Late 1960’s — He received a $25K grant from the National Research Council as a consultant on microscopy. However, this was quickly revoked due to his troubles with the French medical authorities of past years.
1971 — Gaston Naessens began again as a medical researcher. The head of the MacDonald Stewart Foundation (organization which funded orthodox cancer research for many years), David Stewart, agreed to finance Naessens’ research personally and establish a laboratory for him on the MacDonald Tobacco Company’s premises in Montreal. This infuriated the orthodox oncologist on the research wing, and Naessens was forced to move to a low-key spot in Rock Forest on the banks of the Magog River near Sherbrooke, Canada.
1972 — Initial meeting regarding additional funding for research relating to Naessen’s somatid theory and the formula 714-X went well. An assistant professor of pathology, Daniel Perey, volunteered to head the proposed investigation.
Perey visited Naessens laboratory and described it as nothing short of a revelation. However, his excitement was not shared by all. Co-investigators with Perey questioned the validity of the somatid cycle, as this contradicted the definition of disease taught in medical schools.
Late 1972 — Perey extolled Naessens’ contributions to the field stating, “The scope and insight which Mr. Naessens has brought to this area of research potentially stand to benefit mankind and may be a source of pride for Canada!”
1974 — The final report of the MacDonald Stewart Foundation rejected the somatid theory and Naessens’ notion of bolstering the immune system to fight cancer. It now became apparent that Perey, who was to be the chief investigator, had been assigned other duties that effectively used up the time to run the Naessens study. This duty was passed on to a husband-and-wife team of researchers who were not in the least interested in truly researching the brilliant theories of Naessens. Their focus was only on one large form of the somatid cycle that had been described as a bacterium by German researchers who had isolated it in the 1930’s. Overall, they dismissed the stages of the somatid cycle as “artifacts” produced by mistakes during the process required to observe them. Perey’s response in relation to the researchers was, “microbiological dogmas are so entrenched in this couple’s minds that they do not allow themselves the luxury of challenging them.”
Late 1974 — Dr. Raymond Keith Brown, a consultant for New York’s Memorial Sloan-Kettering Cancer Center visited Rock Forest. Brown’s memo to the center read,”What I have seen is a microscope that reveals with spectacular clarity the motion and multiplicity of pleomorphic organisms in the blood which are intimately associated with disease states. The implications…are staggering….It is imperative that what its inventor, a dedicated biological scientist, is doing, and can do, be totally reviewed. I am convinced that he is an authentic genius and that his achievements cut across and illumine some of the most pertinent areas of medical science. If the review of his work is confirmed, this man should be brought to New York and given unlimited support and facilities to continue his research.”
Dr. Brown, along with an oncologist and microscopist eventually drafted a second memorandum that reiterated the first. Unfortunately, Naessens’ name appeared on the American Cancer Society’s “blacklist” and the excitement subsided.
August, 1980 — Naessens supplied 714-X to Dr. Gaetan Jasmin, a professor of pathology and medicine at the University of Montreal who was willing to embark on the standard animal-control test; that is, injecting the 714-X into cancerous and noncancerous rats. Dr. Jasmin concluded the substance had no effect and the results were reported in the MacDonald Stewart foundation literature in 1982. But, Jasmin refused to follow Naessens specific protocol for the use of the substance. He had injected the medicinal into the tumors themselves rather than into the lymphatic system, a procedure he decided was impossible. Whereas standard cancer treatments follow that procedure, Naessens’ truly holistic approach was designed to treat the symptom via the cause — the diametrical opposite of orthodox oncological approaches.
Throughout the 1970’s & 1980’s, doctors and patients alike continued to flock to Rock Forest. The doctors learned about the new biology, while the suffering patients were taught to inject themselves with 714-X or referred to doctors who were willing to treat them. Tremendous results continued as well.
December, 1984 — The police and officers of the Quebec Medical Corporation raided Naessens’ house and laboratory, seizing vials of 714-X and some 150 medical files. Charges would be brought some 5 years later.
1989 — Naessens was brought to trial. Despite the odds, he was acquitted. Witness after witness took the stand to describe the horrors of their battles with cancer and the hopelessness with Western treatments, and the cures they’d finally achieved using Naessens’ treatment. Imposing figures such as the politician Gerald Godin and the French ambassador to the Seychelles spoke passionately on Naessens’ behalf. Even the Quebecois folk hero, Gilles Vigneault showed his support. To the press, Vigneault described what was happening to Naessens as a “witch hunt” and went on to sing the praises of alternative medicine. He concluded: “One must seek, on humanity’s behalf, medical progress unblocked by pharmaceutical lobbyism that, together with that on arms mongers, is one of the world’s most powerful.” The headlines of the Journal de Montreal read “Naessens Acquitted.” A sidebar noted “It’s 25 years now that this farce has continued!”
Late 1990 — After receiving the positive results of nontoxicity tests, Health and Welfare Canada agreed that 714-X could be supplied by Naessens to doctors whose patients were suffering from terminal cancer.
1992 — A growing interest in Naessens’ approach to cancer, AIDS and other such diseases continues to grow. As of October of this year, 210 MD’s across the country (Canada) were administering it to patients. Naessens was also invited to the controversial conference on alternative treatments for AIDS held in Amsterdam in May. This conference was attended by such notables as Luc Montagier, the French scientist who is credited with the discovery of the so called “AIDS virus.” In Europe, the Philippines, New Zealand, Australia and the U.S., physicians are using 714-X with the conclusion that barring total destruction of the immune system, this may be the most promising treatment for AIDS and cancer ever seen. In the U.S. an independent study on 714-X using human patients has been under way since last May.
Commentary
It is very disheartening to see such abuses heaped upon such a brilliant, humane individual. One is reminded of the famous Hindu quote, “In shallow men, the fish of little thoughts cause much commotion. But in the oceanic minds, the whales of inspiration make hardly a ruffle.” However unfortunate, history is filled with such examples of “shallowness.” As Christopher Bird pointed out, the individuals who paved the way for Mr. Naessens — Antoine Béchamp, Geunther Enderlein, Royal Raymond Rife, Wilhelm Reich to name a few — met with similar abuses by the established medical authorities. Nonetheless, much interest continues to be generated by the man who someday will be recognized as another Albert Einstein.
Mr. Naessens’ work is at the forefront of a “new” push in health care; that is, prevention and bolstering the immune system via natural means. For example, AIDS, a disease characterized by subcellular organisms in pursuit of growth due to the presence of a deficient host {personal conclusion}, has been shown to be responsive in some instances to such immune enhancement approaches, particularly when compared to orthodox treatments.( 1) One hopes that future research and grants will begin to focus on this neglected aspect of health care. Also, one hopes that individuals such as Gaston Naessens will have the freedom and opportunity to continue their brilliant work in the field.
Note: Much of the material in this letter can be found in Christopher Bird’s book, The Persecution and Trial of Gaston Naessens. It is an excellent account of the work done by Mr. Naessens. I would also like to thank Mr. Bird for his input into this present article.
(1.) Culbert, Michael. AIDS: Terror, Truth and Triumph. R.W. Bradford Foundation: Chula Vista, CA, 1989.
Townsend Letter for Doctors & Patients.
_____________________________________
CANCER, 714-X AND GASTON NAESSENS
If you looked into a regular microscope at a drop of blood, the way it is done in most laboratories, you would see a still-life picture of bright-red cells, reddish-pink and purple cells. The sample of blood has been treated with dye to illustrate the different cells and nothing moves in this picture.
However, if you looked into a high-powered new microscope called a Somatoscope, invented by an exceptional French-Canadian, Gaston Naessens, you would see a totally different picture. Things move on a black background, seeming to bounce and bump around, and you would wonder if you could see twinkling before your eyes. The `twinklings’ that you see are not your imagination; they are called `Somatids’, and they can illustrate your life force and your state of health. Many conventional medical authorities don’t know what to make of it; some deny it; some admire it; some look the other way.
An investigative reporter with a deep-voiced Georgian drawl, author Chris Bird, told the audience at Health Action ’91 of his investigations into the life and work of the French-Canadian inventor Gaston Naessens. With his natural investigative spirit, he discovered a fascinating story of the suppression of a genius, and the gift that this genius has offered to an unwilling medical community, a new cancer treatment called 714-X.
This new microscope is being used as part of a program for cancer patients available to Canadians. After deciding that 714-X is a treatment that the patient would like to pursue, then it is necessary to convince the medical doctor this is the treatment of choice. Having established that, then the physician is to notify the Emergency Drug Program in Ottawa at (613) 993-3105. A history of the patient is required, and the serum and instructions on administering it will be sent directly from the Naessens clinic to the doctor. Details on how to obtain the Somatoscope, or requests for information, can be addressed to: The Naessens Clinic C.O.S.E. 5270 Fontaine Rock Forest, Quebec J1N 3B6 or telephone (819) 564-7883 or FAX (819) 564-2195. Or, send $15 to HANS [to help cover costs] and we will send you an information package on this topic.
Health Action Network Society.
By Christopher Bird
_____________________________________
A New Answer to Cancer: Microbiologist Gaston Naessens’ immune system therapy 714X has been achieving dramatic results — and irking the “cancer industry.”
Thirty-nine-year-old Jacques Viens had gone home to die. Seven-eighths of his stomach had been removed, and the cancer had already spread to the lymph. Since there seemed to be no hope of recovery, his doctor offered him a new, experimental treatment called 714X. He tried it. Four months later he was healthy enough to go hunting, and not long after that he resumed his job.
Fifty-one-year-old Marcel Caron suffered from intestinal cancer, but he refused to have his intestine removed. His wife’s breast cancer had been successfully treated with the same experimental medicine Viens had used; Caron wanted to try it too. Sixty-five days after he started treatment, no cancer was to be found in Caron’s body. Eight years later, he was still healthy.
These are just two among hundreds of case histories of patients who recovered using a little-known approach to cancer and other degenerative diseases that proponents claim could revolutionize medical practice. The first person to use it — more than 20 years ago — is still alive.
What would happen if an effective treatment for cancer were finally found — a nontoxic, natural, and inexpensive treatment that could be self-administered at home with a success rate of 75 percent? It sounds like a dream come true, a miracle. We would all breathe a little easier, that’s for certain; many lives would be saved.
And a multibillion-dollar enterprise — the pharmaceutical-medical-insurance complex, the most profitable industry in America today — would be forever transformed. Dozens of giant pharmaceutical and medical supply companies would be forced out of business. The “cancer industry” would be no more.
Little wonder, then, that we have heard so little about a 69-year-old French microbiologist who says he’s discovered such a treatment. His name is Gaston Naessens, and he calls his immune-system therapy 714X.
When Naessens’ unorthodox treatment methods began yielding dramatic successes in his native France, French medical authorities closed his lab, confiscated his equipment, and heavily fined him for practicing medicine without a license. Naessens went to Canada, where, with the help of the prestigious MacDonald Foundation (which for years has funded cancer research), he set up a small laboratory outside Montreal. There he and his wife, Francoise, continued their careful research until 1989, when Naessens was again brought to trial by the medical authorities, accused of contributing to the death of a woman who did not recover after using his treatment.
After a long trial, in which numerous testimonies were offered by patients and physicians using his approach, he was finally acquitted. (The full story of the trial is told in Christopher Bird’s book The Persecution and Trial of Gaston Naessens.) Now, a handful of doctors are struggling to make Naessens’ controversial treatments readily available in the United States.
Born in northern France in 1924, the young Naessens was a precocious inventor who built a small, functioning automobile-type vehicle when he was only five, followed by a homemade motorcycle. By the age of 12 he had constructed a plane that could fly. (His mother burned it to prevent him from flying it, however.)
When his university studies of physics, chemistry, and biology were interrupted by World War II, Naessens earned an unofficial diploma from the Union Scientifique Francaise in Lilies, where most of his university professors had fled to escape the Nazi invasion. (He never bothered to pursue its formal equivalent after De Gaulle restructured France, a decision that would later lead to accusations that he lacked a college degree.)
With his mother’s support, Naessens continued his studies on his own. While pursuing the study of hematology, he observed “something moving in the blood,” but the particle was too small to be identified by the optical methods he had at his disposal. Fascinated, Naessens enlisted the help of optical specialists in Germany in developing a stronger microscope.
Called the somatoscope, the microscope itself was a significant scientific achievement. Using a unique combination of incandescent and ultraviolet rays, it allowed him to look at living blood (without first fixing and staining it, which is the usual method) at a magnification of 30,000 times with a resolution of 150 angstroms — a capacity that has not been exceeded to date.
Using this unique method of microscopy, Naessens was able to study what he had glimpsed previously but could not identify: motile microorganisms in the discovered that somatids are resistant to acids and bases as well as heat and that they cannot be cut with a diamond. For example, they withstood 2 megarads of radiation capable of killing any living thing, as well as carbonization temperatures of over -200 C. He concluded that they are indestructible.
Recently, Dr. James F. Ransdell, a pathologist on the faculty of the University of California at Davis, showed me the somatids in my own blood on a TV screen, using Naessen’s “condenser,” an attachment he developed that converts a regular microscope into one resembling his invention. Lots of bright little bodies were busily circulating around the red blood cells, platelets, and lymphocytes in my blood, their motion not unlike that of swarming bees.
Cell division cannot take place without these busy, glowing bodies, Naessens postulates, because in the course of its cycle the somatid releases the growth hormone trephone, which enables cells to divide and multiply. Naessens goes even further — he believes the electrically charged, luminous somatid is the original spark of life, the pinpoint where energy condenses into matter. According to Naessens, the somatid represents the manifestation of cosmic energy in a tiny, moving dot of physicality.
quently attributed to environmental toxicity, by rejuvenating the body’s defenses. Holistic treatments, like the traditional methods from which they evolved, consist of appropriate diet, exercise, and supportive plant medicines to replenish our depleted reserves and restore strength.
Naessens’ theories align with the tenets of holistic practice. But unlike most holistic healers, Naessens is able to provide scientific documentation and evidence of what traditional and naturopathic approaches have suggested all along — that disease represents imbalance in the ecology of the whole organism.
In healthy individuals, says Naessens, the somatid moves through a three-stage cycle that produces the right amount of the growth hormone trephone to keep cells reproducing at the appropriate rate. (This growth hormone was first identified by Nobel laureate Alexis Carrel, who did not, however, link it to a subcellular entity in the blood.)
When the body is stressed or weak, however, the somatid shifts into a longer macrocycle that features 13 additional stages, including forms that resemble bacteria, viruses, and yeast cells. Other scientists have seen some of these forms in the blood of cancer patients and have posited a bacterial and, later, a viral cause of cancer. However, according to these theories (which have not been confirmed by scientific evidence), the disease carrier has always been thought to enter the body from somewhere outside, as germs do. In Naessens’ view, these microbial forms are simply phases of the somatid in its extended cycle. In this amplified cycle, the somatid produces excessive quantities of growth hormone, creating the abnormally rapid cell growth we call cancer.
Naessens is not the first scientist to describe polymorphic entities in the blood. In the early 1800s, Antoine Bechamp, like Guenther Enderlein and many other pioneers, using far more primitive microscopes than Naessens’, perceived microzymas, or “little bodies,” which were thought to be fundamental elements of cells and whole living organisms. When the organism is disturbed by a serious event, Bechamp theorized, the symbiotic relationship between the microzymas and the body becomes imbalanced, leading to disease. In this view, illness originates within the body.
The scientific establishment rejected Bechamp’s work in favor of that of Pasteur, who was convinced that disease is caused by bacteria entering the body from without. Pasteur’s work, which had wide application to a host of infectious diseases, led to the important discovery of immunization. Bechamp’s theory was rejected, and germ theory became a sacred tenet in medicine, despite the fact that a number of diseases do not appear to conform to that pattern. On his deathbed, Pasteur was said to disavow his own theories and exclaim, “[He] is right. The microbe is nothing! The terrain is all.”
In Naessens’ theory, the microcycle of the somatid is held at three stages by blood inhibitors, which consist of certain digestive enzymes, hormones, and minerals. Poor diet and stress apparently reduce the number of blood inhibitors, allowing the somatid to commence its extended 13-phase macrocycle. The presence of these extra somatid forms signifies the beginning of degenerative disease before it has manifested itself in the body. Hence the somatid theory has a valuable diagnostic application, which, in combination with other factors, makes it possible to diagnose and even treat the disease before it takes hold.
The difference between healthy cells and cancer cells is their rate of growth. The somatid macrocycle generates a tremendous increase in the number of somatids, releasing more and more growth hormone into the body and stimulating the rapid multiplication of cells we call cancer. The increasing mass of disorganized cells secrete what Naessens has called the “co-cancerogenic factor,” a substance that allows the cancer to withdraw essential nitrogen derivatives from the patient’s cells and also begins to paralyze the immune system, radically undermining the patient’s ability to combat the disease.
The cancer does not take long to metastasize (spread to new locations) throughout the body. Since the usual orthodox methods of treating cancer involve cutting out, burning, or poisoning the cancerous tumors, cancer’s potential to metastasize has kept everyone stumped. A systemic treatment for the disease would enable the body to again perform its normal function of removing cancer cells, which in healthy bodies takes place almost daily.
According to proponents of the approach, Naessens’ 714X (the name is alpha numerological reference to the letters in his own name) is such a treatment. It is distributed rapidly throughout the body by the unique method of intra-lymphatic injection. Doctors have said such injection is physiologically impossible, due to the structure of the lymphatic system — yet thousands of people have now used the treatment with encouraging results.
714X is an aqueous solution (trimethyl bicyclo mino heptane-CL) consisting of camphor, mineral salts, and nitrogen salts, which is injected once a day for a 21-day cycle. The treatment is then repeated until the progress of the disease is reversed and finally stopped.
The salts help to cleanse and clear the lymph of toxins accumulated during the disease, thereby reviving the body’s defenses, which go back to work to fight the cancer. The nitrogen actually feeds the cancer cells so they do not drain the body’s nitrogen. The camphor carries the nitrogen to the cells and impedes the formation of the “co-cancerogenic factor,” again stimulating the body’s own ability to fight the disease.
(Camphor is widely used by village people throughout India to treat a wide variety of illnesses, from bronchitis to diarrhea. According to Jahnavi Morton, an ayurvedic practitioner who studied under Vasant Lad in New Mexico, camphor is used for “opening the flow of prana, bringing clarity to the mind.”)
A healthy diet that follows the familiar guidelines of holistic nutrition (no sugar, low fat, no dairy, no pork or beef, and so on) accompanies the treatment.
Unlike allopathic medicine’s “magic bullet” approach to illness, the treatment does not do anything directly to the malfunctioning somatid, nor does it attack the symptoms of the disease. All it does is stimulate the body’s ability to regain its balance and defeat the cancer on its own. A healthier organism produces more blood inhibitors, slowing down the somatid cycle. As a result, the amount of growth hormone (responsible for cell division) produced by the somatids begins to decline, so cancer cells do not multiply as quickly. Meanwhile, the body’s ability to destroy the existing cancer cells increases. The cancer does not spread. The tumor begins to regress. The body regains its natural balance. The progress of the disease is reversed until it disappears.
Among the growing number of physicians who are recognizing the efficacy of 714X is Dr. Dietmar Schildwaechter, a former faculty member of the University of Pennsylvania School of Medicine who now directs a cancer rehabilitation center in his native Germany. He came across Naessens’ treatment in 1990 through one of his own patients, who showed marked improvement when, unbeknownst to him, she began taking it. When he found out what she was taking, he began looking into the unconventional treatment himself. He “realized that Naessens had discovered and identified what others had only partially seen.”
“Gaston Naessens’ discoveries,” Schildwaechter writes, “represent a brand new dimension in medicine. His recognition of the somatids as the basic form of life and his furnishing a microscopic means to monitor their cycle are nothing short of revolutionary. His method, offering an instant and highly refined way of assessing every human being’s state of health and their responses to therapy, is second to none.” Schildwaechter is now the chief investigator of the Institutional Review Board (IRB) that is documenting the successes of 714X with the goal of obtaining FDA approval for its use in the United States as an experimental treatment.
Naessens’ treatment continues to be available by doctor’s prescription, so long as the patient is willing to sign an informed consent for the administration of an unapproved drug. In order to be thoroughly familiar with the treatment, all patients (and doctors) should be required to read Do No Harm, a protocol booklet published by Writers and Research, Inc.
Although Naessens boasts a 75 percent rate of success for his unique treatment, how are we to know that this is not just another crackpot cure? Most alternative treatments lack the validation on which Americans have come to rely, the stamp of approval by the American Medical Association, the National Cancer Institute, and the FDA. The august bodies of medical research have demonstrated a reluctance to investigate therapies that have not emerged from their own labs.
Of the 63 treatments on the “list of unproved methods” published by the American Cancer Society, over 40 percent have never even been investigated by the medical establishment, writes Ralph Moss, author of The Cancer Industry. “Merely including a scientist’s name on the list of unproven methods has the effect of damning that researcher’s work and putting a tag of quackery on his efforts.” Gaston Naessens is number 63 on that list. American medical authorities, it seems, have joined the French and Canadian in blacklisting his research.
People like Bird and Schildwaecheter argue that there is sufficient evidence that this treatment should be thoroughly evaluated, not dismissed out of hand — specially considering the tremendous toll taken on the body by conventional approaches like chemotherapy, surgery, and radiation. Great scientific advances have often come from off the beaten track, they argue, the work of brave innovators who have neither the time nor the patience to keep their credentials up to date with established boards. The somatid theory may be one of them.
But the most powerful argument for making Naessen’s treatment available is the example of people like Anne Vignal, wife of the former French Counsel General in Quebec, who went to medical doctors to find out why she had not conceived. They told her her infertility was due to a lethal form of leukemia and that she had only three to five years to live.
Vignal had the good fortune to learn of Gaston Naessens and his ground-breaking work. Five years after being treated with 714X, she is very much alive and cancer-free — and the mother of a healthy son.
Yoga Journal L.L.C.
By Stephanie Hiller
Source: Dr Gaston Naessens - Cancer Cures Plus
Book with a chapter dedicated to Gaston Naessens on page 115:
Education of Cancer Healing Vol. VII - Heretics
Gaston Naessens and 714-X
I have grave doubts about Naessens work.
A crusty old man, undoubtedly a genius, but the somatid hypothesis is rather wild.
It was very hard trying to work with Naessens - in fact impossible.
I sold my microscope in 1999 and have not done any work in this field since then.
Back then we tried to set up a research project - some of the top medical and scientific minds were involved, but Naessens effectively scuttled the project.
So, take a look at my bottom line
Towards a bottom line
and meanwhile...
The following is what I thought in my first enthusiasm...
Gaston Naessens is responsible for several remarkable developments which may revolutionise our understanding of life and bring a major advance in cancer therapy. His work started with the invention of an amazing microscope, the "somatoscope". This led him to the discovery of the Somatid Cycle, and in turn to the development of his serum, 714-X.
The Somatoscope
Naessens' revolutionary microscope, the somatoscope, weaves two light sources (one visible, one ultraviolet) together to produce a third, functionally higher, frequency with which it is possible to obtain a resolution and magnification thirty times greater then with conventional light microscopy . (In conventional light microscopy resolution, and therefore magnification, is limited by the wavelength of visible light - approximately 4000 Angstroms.) Although with the electron microscope there is almost no limit to the magnification, the electrons must be beamed through a vacuum, so it can not be used to look at living material. Naessens' remarkable somatoscope, however, can view live material with a resolution of 150 Angstroms, a magnification of 30,000 diameters. That magnification reveals a whole new world in a tiny drop of blood. The world that Gaston Naessens sees in that drop with his somatoscope is quite different from what we were taught at school! He sees that our blood is alive with a teaming micro-ecology. This is how Gaston Naessens discovered the somatid.
Somatids
In all living plants and animals Naessens observed tiny creatures. He called them somatids - "little bodies". He says that in the healthy organism the somatids have a simple three stage life cycle (a simple viroid form, spores, and double spores). This he named the microcycle. The somatids are symbiotic - they've always been with us, and we need them. However, when the body is under stress the somatids elaborate into a more complicated macrocycle, a sixteen stage cycle. The macrocycle is parasitic and is associated with the development of immune compromised diseases - such as cancer. Naessens' theory is that there are inhibitors in the blood that keep the somatids in the healthy symbiotic microcycle. Under stress these inhibitors may be lost and our friends, the somatids, turn into opportunistic parasites. So, in the 16 stage macrocycle bacteria-like and fungus-like forms grow from the somatids. This elaboration of forms is termed pleomorphism. The somatid pattern can function as an indicator of serious disease. The somatid pattern associated with cancer, for instance, is usually observed in the blood up to two years before the manifestation of the disease. This allows us to get a really early warning when we are headed for trouble or it can be helpful in keeping track of the progress of a preexisting disease. By monitoring the somatid phenomenon we can observe a patient's response to both orthodox and alternative treatments, and to life style changes.
Pleomorphism and Darkfield Microscopy
Although developed in isolation, Gaston Naessens' theories are part of a larger body of work that we may call "the darkfield work". His somatoscope is a very special variation of the darkfield microscope. All those who have worked extensively with darkfield microscopy, with live blood, have come up with similar stories of pleomorphism. In conventional "brightfield" microscopy we send light directly through the specimen, and so we can't see the specimen (thin slices of tissue, including blood, are transparent) unless we stain it canadian propecia. And to stain it we have to kill it. So again, as with the electron microscope, orthodox science, with all its sophistication, looks at dead material. With darkfield microscopy light is shone onto the specimen from the side. We look at reflected light against a dark background. This gives us a highly contrasted image. We don't need to stain the specimen, and therefore we can examine at living material. The darkfield microscope allows us to observe the somatid's pleomorphic cycles.
One of the first scientists who talked about pleomorphism in human blood was Béchamel, a contemporary and rival of Pasteur. He called the little bodies he observed "microzymes". Enderlein in the first half of this century called them "protits". In the 1930s Rife built a darkfield microscope comparable to Gaston Naessens'. He too saw pleomorphism.
Pleomorphism is a natural adaptive response of microorganisms. When the environment allows they are virus-like, bacteria-like, or fungus-like: they metamorphose to suit their conditions. When we are healthy they help us. According to Naessens they produce a growth hormone that is essential for cell division in all plants and animals. Biologist call this sort of mutually depended relationship "symbiosis". However, when we are unhealthy our friends, the somatids, turn on us and become parasitic. But this parasitism is a process that can be recognised by darkfield microscopy and it can often be reversed. Most important, we must find out what stressors caused the problem, and correct the situation.
714-X
Gaston Naessens' next invention was the development of a treatment that he calls 714-X. 714-X is a nitrogenized camphor derivative (trimethylbicyclo-nitraminoheptane). As I understand it the rationale behind this treatment is as follows: Gaston Naessens learned that tumours are nitrogen traps. They steal nitrogen from the body and this inhibits the immune system. By supplying nitrogen to the tumour and the body, the immune system is disinhibited, and the body begins to heal itself. (Camphor has a natural affinity for tumours and, as it is not toxic at pharmacological doses, it proved to be the perfect vehicle to carry the nitrogen to the tumour and the body.) The serum is injected "paranodularly" - that means next to the lymph nodes - so it is absorbed into the lymphatic system where it can act most directly. People close to Gaston Naessens' work believe that 714-X is best used early. While they believe it may save one in twelve of the terminally ill patients who turn to it on their death beds, and maybe one in six of the advanced cancer patients who try it as a last hope, when it is given early in the disease process, they feel that it might help almost everyone. Further, anecdotally, even in advanced cancer, 714-X may greatly improve quality of life.
The normalization of immune function is not only of benefit with cancer; 714-X is also thought to help to stabilize, though not to cure, AIDS, and to be of benefit with other disorders in which the immune system is compromised. To date no adverse reactions or side effects have been observed beyond some irritation at the site of injection.
In 1990 714-X was made available through Health and Welfare Canada's Emergency Drug Release Program and it can now be ordered by any MD. More than 800 patients have received 714-X, and it has recently been transferred from experimental to investigational status.
Gaston Naessens' remarkable work promises a whole new understanding of biology. It leads to a new perspective and, hopefully, a great advance in cancer treatment.
To make his work more widely accessible Gaston Naessens has designed a modified version of the darkfield condenser that allows the observation of the somatid cycle that he discover with his somatoscope. Under the banner of "The Canadian Institute of Alternative Medicine" I purchased Naessens darkfield system and offer the "somatid observation" in Toronto. Phone 416 928 9272 or email normanallan
Darkfield microscopy brings us a window into the body and a road to a new understanding.
Norman Allan, Ph.D., is a research scientist and practitioner of alternative therapies based in Toronto. For more information phone 416 928 9272.
Towards a bottom line
2007: when I was first using the microscope in 1994, I would often damage the sample to one extent or another. Then all sorts of monsters might appear in the sample. Were those Naessans' medusaheads?
Something 's going on. I must write of my encounters with pleomorphism.
While I was learning to use the darkfield techneque I helped initiate and was involved in a wonderful collberative effert with some of the brightest lights in the oncology and academic community and Naessens stepsons (who were wonderfully open, bright, and competant) to study 714X, say in lung cancer, but Naessans said "Non".
Meanwhile my friend Ralph had an enthusiastic encounter with 714 and Gaston that faded when data wasn't open. There are no clinical trials, there is no good data, and that seems to be because of Gaston...
so to me 714-X walked off into the distance,
but pleomorphism?
Bottom line?
714-X is not toxic. For many patients with enthusiasm for the product it has been a blessing, but there is no knowing how many. Naessens was not open and there is no good data on the effectiveness of 714-X.
Quite a number of people call me about 714-X, but there is nothing more than the above (except for some gossip) that I could tell them...
Appended information:-
The Somatoscope: "Two light sources, one incandescent with a wavelength of 3,300 angstroms, the other ultraviolet of 1,850 angstroms, start pulsating, producing a third wavelength. This wave goes through a monochromator which produces a ray. This ray is exposed to a magnetic field (the Zeemann effect) which splits it into parallel rays. One of these rays is treated by a Kerr cell which increases its frequency. This cell is then stimulated by a step generator-oscillator at frequencies which vary from 250 to 1,200 megahertz. The modulation of a visible light frequency ranging from 250 to 1,200 megahertz produces a basic frequency ranging from 250 to 1,200 megahertz, but also harmonics at a higher frequency (if we use light in the order of 2,000 �). ... the resolution of this instrument is in the order of 150 � and the power of its magnification varies from 2,000 to 30,000." (Gaston Naessens)
Pleomorphism: In a scientific article published in 1992 it was shown that yeast, starved of nitrogen, undergoes pleomorphic transformations. This work both parallels darkfield's pleomorphism and vindicates Naessens' rationale for 714-X. (Gimeno et al. Unipolar Cell Division in the Yeast S. cerevisiae Lead to Filamentous Growth: Regulation by Starvation and RAS. Cell 68:1077-1090. March 20,1992)
Cancer and Pleomorphism: "The number and forms of the bacteria seem to mirror the state of systemic sickness in cancer patients, and, by following the appearance of the blood by darkfield microscopy, the patient's therapeutic progress can be monitored." Macomber. Cancer and Cell Wall Deficient Bacteria. Medical Hypotheses 32, 1-9, 1990.
Read full article, with accompanying images and references at: http://www.normanallan.com/Med/714.html
THE SOMATID THEORY AND PLEOMORPHISM
by Dr. Lawrence Wilson
© May 2016, L. D. Wilson Consultants, Inc.
All information in this article is for educational purposes only. It is not for the diagnosis, treatment, prescription or cure of any disease or health condition.
This is one of the more unusual articles on this website. The science is not proven, but please have an open mind. I am hardly the first person to write about this topic.
The somatid theory can definitely help explain newer medical findings that the human intestine is producing many vital chemicals such as hormones, vitamins, and immune system components.
Definitions. Somatids are a type of small, less differentiated body cells found everywhere in the human and animal bodies. Most live in the small intestines, and most are made by mitosis in the brain.
Mitosis means a cell splits into two small ones.
Similar to trophoblasts. In size and functioning, somatids are similar to Trophoblast Cells, discussed in a separate article on this website.
Totipotent. Trophoblasts are almost totipotent cells. The word totipotent (total potency) means they can turn into any other kind of cell. Somatids are similar to this and may be the same, in fact.
Generalists. Most cells, early in their lifespan, differentiate. To differentiate means the cell becomes a specialist. Some cells become stomach tissue, while others become skin or hair. Others become the eyes, the nose, or some other body tissue. The cell remains this way for the entire life of the cell. Somatids, in contrast, can change their form and their functions.
Pleomorphism. The quality of changing one’s form and function is called pleomorphism. The word just means having many forms. So one can say that somatids are pleomorphic. This just means that they can change their form and function.
DISCOVERY OF THE SOMATIDS
Somatids were first found in modern times about 110 years ago when several European scientists with special microscopes noticed them. One needs a special microscope because most microscopes, including the most modern electron microscopes, require killing cells first before you can look at them.
If one kills the somatid, one will not see the cell change its form or function. As a result, the idea of a cell that changes itself depending on its environment is not currently accepted in medical science.
The scientists who discovered somatids had special microscopes, known today as Rife microscopes. These are very rare instruments, and there are very few of them on earth. They turn the specimen into a light source, and as a result can get extremely high resolution on a live cell.
The somatid discoverers. The first scientist to see them was Antoine Bechamp, MD (1816-1908) in France. He called them mycozyma. Some people still use this term, but most prefer the word somatid. He saw that they changed their form depending on the terrain inside the body.
As a result, he believed they were the basic building blocks of all organisms, even plants and rocks. In this, I believe he was incorrect. Not all cells are somatids. However, he was correct in identifying the somatids as very unusual.
In the early twentieth century, several other scientists observed them. A Canadian doctor, Gaston Naessens, MD (1924- ) called them somatids. Guenther Enderlein (1872-1968), a German physician, called them protits. The name somatids is most accepted.
Another who observed them was Royal Rife, MD in the United States. All these scientists wrote about these cells, and designed remedies based upon them, as well. To read more about Dr. Rife, Dr. Naessans and pleomorphism, read The Cancer Pioneers on this website.
MODERN SCIENCE DOES NOT RECOGNIZE SOMATIDS
The concept that a cell can change its basic form has found only limited acceptance in the medical world. For example, it is known that many yeasts are dimorphic. This means they have two forms.
They have both a mold or hyphal form, and a yeast form. Among such yeasts are some penicillins and the common candida albicans. Somatids are somewhat like this – able to change their form depending on the conditions inside the body.
The medical establishment considers somatids part of esoteric or occult science, but it is no such thing. It is simply science that is more advanced, or harder to see.
SCIENTISTS DISCOVERING THAT THE GUT DOES MORE THAN DIGEST FOOD
One of the more modern discoveries of medical science that is mostly still unknown among doctors is that one’s intestine is not just a place to digest food. It contains immune cells, and many others. This may be because of the presence of the somatids.
In fact, a popular diet for autistic children is called the Gut And Psychology Diet or GAPS diet, for this reason. To read more about this, and why I don’t recommend it, please read The GAPS Diet on this site.
ARE THE PLEOMORPHIC FORMS PATHOLOGICAL?
Gaston Naessens and other researchers believed that the pleomorphic forms of somatids are abnormal and pathological. This appears to be true, although some scientists debate this point.
ARE SOMATIDS THE SAME AS PROBIOTICS?
No. The somatids are not the same as what are called probiotic organisms. The latter include various strains of bacteria such as lactobacillus acidophilus, for example. These are cells that cannot change their form or function. In contrast, somatids can change their function.
The somatids are also different from what are called ferments in the intestines. These are various bacteria and yeasts found in foods such as yogurt, sauerkraut, miso, cheese, kefir, and a few other foods. Differences between somatids and probiotics include:
1. Compared with the souls in bacteria and ferments, the souls in the somatids are much more advanced.
2. Somatids are not just found in the intestines, as are the probiotic organisms. Somatids are found everywhere in the body.
3. Somatids can move in and out of body organs easily because they are extremely tiny. Probiotic organisms are much too big to be able to do this.
These are just a few of the differences between somatids and other micro-organisms in our bodies.
IMPORTANCE OF FIXING THE TERRAIN OF THE BODY
The implications of the somatid theory are enormous, including the following:
1. If the terrain of the body is this important, then diet, lifestyle, rest, sleep, thoughts and emotions should be the focus of our health care system, not drugs, surgery, vaccines, fluoridation and other toxic methods.
2. If terrain is important, detoxification of the body is critical, as nutritional balancing asserts.
3. If terrain is critical, then keeping the body pure in all ways should be the goal. In addition to a pure diet, one’s lifestyle, morals, character development and careful education of the young are therefore of the greatest importance.
FINAL REPLACEMENT OF THE SOMATIDS
If a person follows a nutritional balancing program for at least 20 years, causing development, the somatids atrophy, and eventually disappear. This may occur when the down force through the body is strong enough. To read more about this, please read Downward Moving Energy And Healing on this site.
The replacement of the somatids is one of the goals of every nutritional balancing program. However, to the best of my knowledge, final somatid replacement is not discussed among doctors who endorse pleomorphism and the somatid theory. Most likely, this is because they do not know how to accomplish the replacement of the somatids.
Source: http://drlwilson.com/articles/SOMATIDS.htm
Manufacturer's webpage with multiple official company YouTube videos which are hidden on YouTube itself, about 714X, a screening test, somatid and its pleomorphism and the somatoscope:
Media | Cerbe Distribution Inc
Basically this is a cancer medication which has to be administered by a doctor in Canada or Mexico and has a big success rate to date according to sources. The 714X (the anti-cancer agent) product is still manufactured, with cGMP quality, sold and used by clinicians to this day in Canada and Mexico. The somatoscope is still in use by scientists, so far as sources state. The 714X product can be found on the manufacturer's website here:
Cerbe Distribution Inc | A Trustworthy Partner for Better Health
Mr Naessens has sadly passed away this year at the age of 94.
French news article about his passing: Le chercheur Gaston Naessens n’est plus
I hope this topic will be used to discuss the works of Mr. Naessens and his cancer treatment and that it will help people when it comes to cancer treatment options and discussion.
CC: @burtlancast (From who I came across Naessens and 714X, thank you for that, Burtlancast!)
Last edited: