On the Cure of Cancer and Many Other Chronic Illnesses

A Medical Essay on

the Cure of Cancer

and Many Other Chronic Disorders

by Boosting the Immune System and/or by

Neutralizing DNA Destabilizers

Some physicians attribute cancer's main cause, and that of many other diseases, to a fungus. Others implicate bacteria or viruses.

What's their evidence? Not that these microbes, when put into the body, cause cancer. No. Instead, after an autopsy or biopsy, they visually see under the microscope that tumors have embedded in them these microbial shapes, to suggest fungi, or other microbes as the culprits. The correlation is inevitable.

But this hind-sighted approach, namely, seeing it upon death or in an advanced case biopsied, is what implicates these agents as the significant agents of disease.

Actually such an assertion violates the priciple that "correlation does not prove causation".

You can ask: "Well, then why are these microbial shapes found -- in almost all tumors -- found at autopsy or biopsy, if they're really not the prime movers of the disease?" Maybe these foreign agents snuck into the body and, without first causing an entry-point infection, they snuck past the intervening membranes and then internally set up shop to begin infestation from within.

The remarkable biology introduced by Dr. Gaston Naessens in France a few decades ago will yet revolutionize the study of biology just as had the findings where the atom, first thought to be an element of itself alone, was later found to consist of hundreds of subatomic particles. The latter findings lead us into the new field quantum mechanics. (E.g., LINK, LINK)

The Somatid Cycle discovered by Naessens, among other fascinating discoveries, has yet to be appreciated so fully. I'll wager that not even one Western university even teaches anything about this grand master of medicine.

It was Gaston Naessens who demonstrated with his new "somatid" discoveries, that some stages in the cycle of this subcellular particle have the same morphology as do fungi and bacteria (depending on the stage in the cycle), how environmental deterioration, or the degree of cellular stress, creates a metamorphosis of that somatid particle do undergo a transformation, the first stages of which resemble bacteria, and with additional stress, albeit reversible, to fungal structures.

Logic would therefore dictate to reverse the stress factors and these, in turn, will alleviate bacterial or fungal "infections", rather than focusing on the underlying morphological aspect and treating that. For treating the symptom is not a solution. Imagine, for example, upon seeing "bacteria" inside a tumor's mass, the physician prescribes an antibiotic. Because of this new cellular stress, however, we can expect the fungal phases of that somatid cycle to kick into the worsening, fungal stage.

Unfortunately, Naessens' brilliant discoveries and curative methodology is darkly secluded by the BigPharma mafia that control many Western governments in some remote town in Quebec, Canada. Thankfully his family continue the pioneering work.

For example, Dr. Nassens' unique administration of a simple nitrogenous camphor molecule, drained into the lymphatic network of the groin (&/or via pulmonary lymphatics), reverses the distress of the cell and reverses the stages underwent in somatid metamorphosis, and, almost incredibly, seems to "liquify" the lymph circulatory system as well as somehow activate or boost the immune system into self-preservation. The immune system can then be expected to fight off the symptoms experienced so far, and indeed reverse the disease -- or cancer.

This boost given to the immune system is seen from an entirely different area of research and of different countries. Just as Naessens modulated lymphatic mediation, which boosted the immune response, so too a simple protein, when injected into the groin, is found to round up and activate the macrophages, the fighting soldier cells of immune system, to devour and destroy the intruder or subverter. That product is called GcMAF. This Vitamin-D derived simple protein has a branch on which reside 3 sugars. A lymphatic B-cell clips off one of these. The lymphatic T-cell clips off another. The protein with its one remaining sugar now works as a key. As it locks into a Macrophage's "skin", it immediately goes into offense mode, immediately responding with exploratory and offensive behavior, either by devouring or exploding the intruding structures.

That thrust of the immune system into high gear, stimulated by GcMAF, has a natural enemy that can, for whatever odd reasons, sometimes render this immune system's mechanics to falter. It's been discovered (on different continents at the same time) that an enzyme, said to be the secretions left by viruses -- or by cancer cells -- which, much like the wrench thrown into an engine, can trick the immune system into being "tolerant", or "restful", thus remaining inactivated. This sectreted substance by the cancer cell (or by the virus) is called Nagalase. This enzyme attacks that Vitamin D-derived protein with a stem of 3 sugars -- by clipping off that stem that holds all 3 sugars, leaving what remains as a "useless key" that cannot activate the sleeping macrophage.

But now that we know this interplay of two molecules, between GcMAF and Nagalase, the latter substance can easily be overwhelmed by raising the amount of GcMAF introduced. The result is: a reinvigorated immune system that will sure enough reverse itself from disease to wellness. (E.g. LINK, LINK)

Another great pioneer of Medicine, Mirko Beljanski, showed clearly the main cause of cancer. He demonstrated that the partial unravelling of the DNA molecule, from its usual double helix structure, is the cause of extra cellular RNA and DNA activity, which leads to cancer. He showed how poisons attach to the DNA molecule and thereby break the core hydrogen bonds, which then yield a "destabilized" configuartion. The helix is no longer the same tightly bound helical structure; Now loose strands of it are exposed to the cell's milieu, which leads to undesired toxic effects. Not because the DNA genes have changed, but that some parts of the DNA chain lost their original shape. The attached poisons, because they have impact on the structure by attaching themselves to the DNA molecule, leave some DNA parts exposed, and these loose filaments then stimulating unwarranted cell activity. He showed how removal of these poisons, or by introducing certain herbal substances that counteract the poison's ability to change the shape of the DNA molecule, reversal of the toxicity can be achieved. (E.g., LINK, LINK)

Beljanski's therapy seeks to eliminate or reverse cellular stress or toxicity. The other two therapies alluded to above, achieve similar results via enhancing the power of the immune system. This, using one (or both) of the former methods achieves the same reveral only that it's done by boosting the immune system. Beljanski's herbal extracts may or may not have also included this effect, but if it did it did so in a way we're yet unaware. It seems that Beljanski's approach was more direct and aimed at reversing the poison's hold itself. The immune-boosting therapy and the herbal extract method that neutralizes the poison - of course can work in tandem for better results, I'd wager.

To get the immune-boosting products, because the FDA had come out against it, one just needs to know where to get the products and from who. How long the exemplary links herein offered will hold up, before BigPharma clamps down on them, is anybody's guess.

(Those who want to learn more have herein enough to further explore with.)

Dr. Jeff Bradstreet and Autism

Dr. Jeff Bradstreet discovered that “Autism is viruses in the brain and viruses in the stomach”. This definition, impressive as it is, also brings new insight into “viral” disease that none is aware of - unless they know the work of Gaston Naessens (see prior post for more on him).

Naessens discovered a tiny particle in cells without which the cell cannot survive!

These subparticles, in the nanometer  Naessens called “somatids”. He found that these extremely tiny particles can undergo morphologic changes, the entire range spanning 16 stages. The latter stages, from stage 4 to stage 16, are degenerative stages, whereas the first 3 are the normal, undistressed stages. Significantly, he showed too that the somatid's latter stages can be reversed by removing cell toxicity or by boosting the immune response.

The longer the cell remains toxic, the more likely the somatid's later stages will actualize. Relief of stress bring recovery to the cell as the degenerative stages go into reversal. From the 4th stage onward, the stages go from bad to worse. Or, disease can be vanquished in which case only the 1st 3 stages are to be seen.

The early degenerative stages resemble forms of virus. Further degeneration creates forms that resemble bacteria, and severe degeneration creates forms resembling fungi.

So when Dr. Bradstreet (probably assassinated by the FDA [and the list gets bigger]) said the autistic child has a multifocal viral infection, (detectable by measure of the enzyme nagalase in the blood), he was probably very accurate.

Naessens ingenious remedy was to flood the lymph with a nitrogenous natural compound that "liquified" the lymph and gave the immune system a boost to again take control of the body.

Jeff Bradstreet was able to cure many autistic children -- also by modulating an immune response. How did he revamp the immune system? He found that probiotics offered an easy and delicious way to recharge the body's immunological system. It happens that the immune system suffers shock, for whatever reason, and goes into a dormant state, but plenty of evidence now shows that that lethargy can be overturned. The new bacterial populations, it turns out, give us a natural means by which to vitalize the body’s defense mechanism, much like supplying a carpenter the hammer he needs to drive his nails.

Bradstreet and others found the cultures had been effective. They cured hundreds of children by providing this therapy in the clinic. It was working. All along the doctors thought their good results derived from a protein called “gcMaf”. Now newer research, as Dr. Marco Ruggiero of Italy has discovered, attributes an even smaller segment of that molecule as responsible for the positive spurring effect. In isolation of the rest, this tiny molecule provided the turnaround all by itself! That part of the previous molecule now did the trick on its own. He named his serum “Rerum”.

And much like Naessens had the ability to detect the rise or fall of disease, here too an enzyme has been found as the relevant marker.

The one point of contention that might arise between these two scientists, whether or not the viruses arrive into the milieu as invaders from the external environment, or whether they arise internally from the body’s own tissues.

What the Bradstreet doctors attribute to external viruses I believe are, in fact, virus-like forms produced from cellular somatids. The body, after all, came from the soil and will return to the soil (Gen. 3:19), so how will they “return”? Will they necessarily be gobbled up by scavengers from the outside, or, does the body itself “know” how to disintegrate itself? This harks back to the century-old controversy of Pasteur vs Beauchamp. Beauchamp's claim was that the terrain is the important health factor in disease; Pasteur believed the culprit was an outside invader on the attack. Beachamp's view has been the long-shot view now for over 100 years. I concur with Beachamp's thesis that it’s the terrain - not the agent - that mainly determines health or disease.

The List of "Abused by BigPharma" Keeps Growing

Now, with more world-wide internet windows opening us up, windows safely removed from reach of the crooked rich, BigPharma for example, more ways are being discovered how to enhance the body's ability to recuperate from disease.

I may have written earlier of two recent giants, both who were oppressed in France, one being Mirko Beljanski (now taken from us), and the other Gaston Naessens (hopefully still living healthy in Quebec [UPDATE: Sad to report, he passed away Feb. 2018]). Beljanski showed that DNA's destabilized structure, where some zippered DNA becomes partially unzippered at some loci, as the core problem of cancer, and then went on to find ways of curing cancer. In other words, the unraveled portion of DNA can be twisted back into good shape nicely zippered up, but leaving it partially unraveled changes its structure and can lead to unwanted DNA replications. He could also determine the cancer potential of any substance with his simple but ingenious "Oncotest", which simply looked at light coming in from the "cracks" in the DNA configuration. He explained why this "destabilaztion" of DNA caused cancer - as the rule - ruling out "mutations" (which would be the exception) as the primary cause.

Naessens, after ingeniously building a brand new microscope to provide nano-length perspective, he would use this new vision of live blood and, with this better eyesight, he discovered a brand new biology. He actually identified a new particle nobody had seen before, certainly not as close as he saw them. He not only redeemed these as particles living on their own, heretofore thought of as human artifact, he noticed the whole slew of stages this particle could metamorphose into, showing there was 16 different stages in the entire range. The first three were normal, as in healthy blood, and the others, convey that the cells in the blood are under distress. Finally he was able to isolate these particles, which he calls the "Somatid". He found them to be indestructible ?or nearly so? Moreover, and here the new biology begins, for he shows how these somatids could regenerate DNA and cultivate a new host of new viable cells, each properly equipped with recombinant DNA.

When I read of this pre-DNA particle, the precursor to the DNA, I thought of the somatid as God's "G-d particle". After all, if every thing derives from Hashem, you'll always find therefore that the deeper you get into the miniature, the more you see the infinity there too imprinted.

This particle substance, DNA's precursor, the "somatid", is a particle heretofore never seen by man. He shows the 16 stages of the somatid's metamorphosis nd what each stage looks like. Well what do you know -- the different stages appear spore-like resembling viruses or spores, then as string-shaped bacteria, and finally as yeast and fungal shapes. And wow, you can reverse the process! Just remove the stress, and recovery takes place.

This makes so much Torah sense too, because when man returns to earth, from which he was fashioned in the first place, the body knows "on its own" how to disintegrate itself and, as in says in Gen.3:19:
"With the sweat of your face you shall eat bread, until you return to the ground, for you were taken therefrom, for dust you are, and to dust you will return.") In other words, those buggers that eat up our bodies when we're dead don't come at us from the outside; Nope; In the main, they come from within us, from our own cells, programmed to disintegrate already built in!

These giants' discoveries have enormous ramifications for medicine, which itself anyhow needs a swamp-busting overhaul.

So now, with Beljanski's Oncotest, we can easily detect which substances are cancerous, which can reverse the damage; And with Naessens help it's so easy to detect from a drop of blood. It may be added here, to add praise to Naessens, in that he too found ways to reverse and/or heal chronic disease -- by injecting lymph canals with a simple nitrogen-camphor.

Being able to predict and prevent disease is now simple and inexpensive. We have a new biology that never yet made it to college, let alone to "med school".  We have open to us a fascinating, yet simple, non-drugged way to revitalize the body, by revitalizing and reawakening the body's innate lymphatic immunological potential.

More windows open up meanwhile.

But pay notice to the one common thread that ties all these incredibly able people and scientists, which they all share. That predominant feature that they possess is -- all of them must live on the run, always alert to avoid the BigPharm's corrupt and immoral grip on "medicine".

The latest I learned of, whose work and life are full of merit, is Jim Humble, now forced to live in Mexico. Another great American having to protect himself from palpable harm living in his home country. That's where he escaped BigPharma's tentacles. (Heard about the murder in Turkey of that Saudi turncoat ["Khashoggi"] whose own crown-prince had him assassinated in Oct. 2018? Well, even America, land of the free, has its share of bad boys among government bigwigs, and BigPharma/FDA is one of them.

I'm reading his great book, MMS HEALTH RECOVERY GUIDEBOOK. From Mexico he provides powerful knowledge to the world at large, for the sake of humankind. I admire the guy. His perspective clashes and contrasts with the mean and sore control of health of today. Allopathy only offers stuff from its own, patent-hungry labs. "Alternative medicine" is sourced and created in God's laboratory.

The product touted by Humble, and now by many many more, is a powerful, tiny, oxidizing molecule, chlorine dioxide. I think I got that right. He calls this agent MMS. (e.g.: link). He then went ahead to formulate protocols for so many conditions. I'm now rereading

Do research. Sense the miracle. But be forewarned, try to bypass the nuisance of BigPharma teamplayers. They try to create a mine-field so you get fed up researching material issued by herbal or natural prescriptions. Seek out if you can the originator's mind because those looking to divert focus from truth find many ways to set before you obstacles.

Poor Humble must live out his life in Mexico. At least he gets much more freedom in Mexico than he would living, believe it or not, in Canada! Just see how they marginalized Mr. Naessens from his life-long dreams, offering him the bare minimum just to survive. (He must be 96 by now. May God grant him, and Humble, a long life!) In Canada, as with France and England, and as here in the U.S., BigPharma thrives and rules the roost, and has ruled it now near 100 years.

Article on Gaston Naessens

I wrote about Naessens in the previous post. This post can be considered its follow-up, a great piece about Naessens and mind-blowing.

The author of this article, Paul William Roberts, received the Journalist of the Year Award for this article which was published in the Toronto, "GLOBE AND MAIL" weekend insert magazine called: "SATURDAY NIGHT", Dec. 1992. [seen here]

BLOOD FEUD
by Paul William Roberts

Gaston Naessens claims to have discovered a new way of looking at blood that could revolutionize the treatment of cancer. Why does the medical establishment consider him so dangerous?

In 1989, a French-born biologist named Gaston Naessens was arrested in Quebec and charged with four counts of illegal practice of medicine and one count of contributing to the death of a patient.

The patient, a woman with metastasized breast cancer in the terminal stages, had refused all conventional treatments and insisted instead on taking a camphor-based medicinal that Naessens had developed.

The medicinal, which he called 714X, was designed not to destroy cancer cells in the way of conventional treatments but to bolster the immune system and help the body heal itself.

Naessens, who had a tiny private lab on the banks of the Magog River in the Eastern Townships, had instructed a close friend of the woman's in how to inject the substance into the lymphatic node in the groin. She received injections for seven months before she died in July, 1984.

The prosecution wished to prove that Naessens' patient might have stood a chance if she had pursued conventional treatment. The corollary was proving that Naessens knew his alternative treatment to be worthless -- that he was a charlatan hoping to profit from the desperation of someone in the throes of terminal illness.

The prosecution was not fooling around -- the charge of contributing to the woman's death carried a potential life sentence.

The trial, which made the front pages of Quebec newspapers for three weeks in November, 1989, opened with a parade of doctors and scientists testifying to the scientific untenability of 714X and the spurious nature of Naessens' theories of cancer and its treatment.

In the media, a sketchy, negative image of the man began to emerge he claimed to have invented a microscope that could reveal the mysteries of living blood. He claimed to have discovered, through his studies of blood, something he called a somatid, which he said was a precursor of DNA and the absolute ground zero of life.

He claimed to have identified a sixteen-stage cycle through which the somatid passed, and claimed that he could link the various phases of that cycle with the health (or ill health) of a patient.

He'd drawn the ire of medical authorities in his homeland he'd been forced out of France twenty-five years earlier. He'd set up in the quiet backwater of Quebec, his critics said, hoping to evade medical
scrutiny.

By the time the defense was ready to present its case to the jury, the mood was grim in the Naessens camp. But it soon changed. Witness after witness took the stand to describe the horrors of their battles with cancer and the apparent cures they'd finally achieved after using Naessens' treatment.

Gerald Godin, politician, journalist, poet testified on the biologist's behalf, outline his struggle with a brain tumor that he believed 714X had helped to check. The French ambassador to the Seychelles told a similar story.

In the courtroom the gratitude to Naessens was so apparent and emotions running so high that the prosecutor not to cross-examine defense witnesses on "Human grounds."

Moreover, the testimonials to Naessens integrity were overwhelming: He'd never promised a cure, never told one of them to discontinue conventional treatment, and never asked for payment.

When Gilles Vigneault, chansonnier and bard, a Quebecois folk hero, arrived from Paris to show his support for Naessens, the effect was electrifying. To the press during a court lunch break, 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 of arms mongers, is one of the world's most powerful."

The jury was not long in coming to a verdict: Acquittal on all five counts. The Journal de Montreal went to town, its front page headlined NAESSENS ACQUITTED.

A sidebar, however, bore the headline "It's Twenty-Five Years Now That This Farce Has Continued," quoting Dr. Augustin Roy, the head of the Quebec Medical Corporation, the professional self-regulating and licensing body that had pushed for charges to be laid against Naessens.

The Trial, Roy said, was "wholly incomplete" the prosecutor should have "savagely cross-examined every one of the patients who had testified on Naessens' behalf....

"All the patients who testified simply don't know the difference between feeling healthy and being healthy... All of them should stand at attention or, more properly, get down on their knees to thank
orthodox medicine for having kept them alive."

Roy apparently had not noticed that the majority of Naessens' patients were refugees from conventional medicine, which had either written them off or offered a treatment that frequently seemed worse than the disease.

And Roy was not about to relent. Within weeks of the not-guilty verdict, eighty-two more counts of practicing medicine without a license were brought against Naessens, each carrying the threat of a $5,000 fine.

As was clear from this rhetoric, Augustin Roy wasn't fighting any more to protect innocent patients from an unscrupulous quack. He was fighting to protect his profession from an alternative vision of healing, an alternative model of disease processes, and a press that kept on insisting that this heretic, Gaston Naessens, was the Galileo of modern medicine and the microscope.

Naessens himself prefers a comparison with Antoine Bechamp. Not so well known as Galileo and not so persecuted for his "heresies," Bechamp, a professor of biochemistry and dean of the Faculty of Medicine at the University of Lilles, France, in the last decades of the nineteenth century, had been Louis Pasteur's major adversary.

The controversy between Pasteur and Bechamp -- now a forgotten episode in medical history -- had been the scientific equivalent of front-page news and concerned the very nature of disease itself.

Bechamp believed that the cause of disease lay within the entire system of the body Pasteur insisted that disease came from without, which fitted with the formulation of his now famous and standard germ theory. It seems likely that both men were right to a certain degree, but Pasteur was a tireless self-promoter while Bechamp was diffident and somewhat reclusive.

Pasteur's model was also more appealing to physicians who wanted a definite disease target on which they could make war, rather than a state of good health they had to delicately maintain. Thus: the Pasteur Institute, on the one hand, and on the other, a baffled shrug from most doctors if Bechamp's name comes up.

Under his microscope more than a century ago, Bechamp had observed in fermenting solutions tiny particles, which he called microzymas, that appeared to have powerful catalytic effects -- facilitating change while remaining essentially unchanged themselves.

He went on to note the presence of these particles in the bodies of animals, coming to the conclusion not only that they were the most fundamental form of all living matter but that they were essential to any form of life, from cell division and basic bacteria up.

What seemed most extraordinary to Bechamp was the observation that the microzymas could apparently actively participate in the destruction of an organism without being destroyed themselves.

Indeed, their indestructibility was such that he believed a French paleontologist had found evidence of them in 60 million year old limestone from the early Cenozoic era, the period when mammals first
started to develop on earth.

How Naessens became Bechamp's inheritor is a bit of a convoluted story. The youngest child of a banker, Naessens was born in 1924 in Roubaix, near Lille in northern France. As a child he showed a mechanical proclivity that both amazed and terrified his parents. From manipulating Meccano sets at five the boy went on to build his own motorcycle and then an airplane just big enough to carry him -- which his mother burned before it could take its maiden flight.

The Second World War broke out as Naessens was beginning to study physics, chemistry, and biology at the University of Lille. When the Nazis occupied the city both he and his professors ended up in exile near Nice, where he continued his studies towards a degree.

Naessens received a diploma from the Union Scientifique Nationale Francaise, the semi-official institution that operated during the chaotic conditions of the war. But in what turned out to be a typically independent fashion he never bothered to ask for the formal equivalencies the de Gaulle government issued after the war. Consequently, he's been accused of having no academic credentials.

The young man went to work in a laboratory for blood analysis, and hated both the routine job and the imprecision of the microscopes he used. Blurrily he was able to observe something in the blood that had so far not been defined: other researchers had seen it, too, and called it "dross in the blood."

He needed a better instrument. Searching the literature for research on blood and microscopy, Naessens learned of a nineteenth century French biologist now best known as the "noon lunatic."

Emile Doyen claimed to have observed through an ordinary microscope particles in human blood that were visible only around noon during the months of May and June. Naessens was as willing to laugh at the notion as anyone, but began to wonder whether there was any scientific explanation of Doyen's findings. There was: During May and June, in the south of France and at around noon, the natural light available to anyone using a microscope contained far more ultraviolet light than at any other time of the year.

The work of the noon lunatic became the basis for the microscope Naessens went on to develop in the late 1940s, working in a lab funded by his mother at the family home in Lyon.

An extreme and as yet un-duplicated version of what is now called phase of dark-field microscopy, Naessens' instrument allowed him to examine living blood not only at high magnifications but with extremely high resolution.

Although an electron microscope can approach 400,000 X magnification, it can do so only with fixed and dead tissue. Naessens' microscope, which identified particles with light refraction rather than staining, could approach 30,000 X with living tissue at a resolution of 150 angstroms (one angstrom is one-hundred-millionth of a centimeter).

The uniqueness of the microscope has to do with the way Naessens manipulates the light source to achieve that extraordinary resolution. (Several optical companies have approached him over the years but Naessens has been unwilling to give over control of his life's work to big manufacturers.)

What the tool unlocked for Naessens the researcher was a deep view -- the deepest and as yet unsurpassed view -- into the processes of living blood.

Naessens started by looking at preparations of his own blood -- pricking his finger, transferring the drop to a slide, watching until the fresh blood began to clot.

Through his microscope, he observed what he maintains are Bechamp's microzymas: the most fundamental particles of living matter that exist. He called them somatids (tiny bodies) and through seven years of observation concluded that they appeared to play an extraordinary role.

No cell division was possible without them they were seemingly a precursor to DNA, and probably the bridge between energy and matter. He found them all but indestructible, surviving carbonization temperatures of more than 200 degrees C and 50,000 REMs of radiation (more than enough to kill a person) they were also unaffected by chemical agents.

With a better tool to use, Naessens could go way beyond Bechamp, who was able to see only the largest of these microzymas. Naessens observed the somatid in human and animal blood to develop in a form-changing cycle.

The first three changes of this cycle -- somatid, spore, and double spore -- were apparently not only normal in healthy organisms but crucial to their existence in that no cell division could take place without them. Having studied what he took to be healthy blood, he began to study blood from people he knew to be diseased, referred to him by physicians. Unhealthy blood looked drastically different, and exhibited somatids in not a three-stage but a sixteen-stage cycle.

The other thirteen stages were apparently the result of an immune system under stress, and seemed to signal the likelihood of degenerative disease up to two years before any symptoms appeared in the organism.

Naessens began to believe that with observation of the somatid cycle -- in effect, monitoring the physiology of blood -- he could figure out when it was possible to intervene to prevent illness.

Take cancer, for instance. Every body every day produces a few cancer cells and a normal immune system destroys them. But when that system comes under stress, its ability to fight is impaired and the cancer
cells proliferate.

When the ovum is fertilized by a sperm, growth (or cell division) begins: two, four, eight, and so on. There are many such divisions before cells begin to specialized, some becoming skin, some liver, some heart, and so on.

This specialization is controlled by a series of growth hormones that "talk" to the various cells' nuclei. These intracellular commands come from various sources -- lymphocytes, for example, controlled by one, liver cells by another.

In normal circumstances, the growth hormones are controlled by inhibitors in the blood, but when a system is stressed these inhibitors diminish and more growth hormones are liberated.

The result is almost a reversal of the cells' "education." They return to a simpler state, losing their individuality and "remembering" only basic functions from their origins, chief of which is the ability to multiply rapidly and chaotically.

This, it is thought, is malignancy, the pathological cells resembling primitive organisms that have forgotten everything they have learned.

Naessens, through the microscope he called a "somatoscope," was able to observe the consequences of the minimution of sanguine inhibitors and the liberation of the growth hormone by watching the three-stage somatid cycle in the blood suddenly proceeding on through its full sixteen polymorphic stages -- before patients had any conventionally diagnosable sign that they were ill.

His next challenge was to figure out how to bolster the immune system to correct the imbalances in the body that led to disease. He began experimenting with ways to combat the effects of degenerative or cancerous cells by neutralizing their mode of replication -- developing a series of novel anticancer products.

These early medicinals proved effective enough over a fourteen-year period for Swiss and German pharmacies to put them on sale and for numerous doctors to administer them to patients. (By 1964, more than 10,000 people had been treated.)

On the strength of his sales, Naessens was able to move his lab to Paris in the mid-'50s.. But in Paris he came to the attention of French medical authorities, after complaints from some pharmacists and physicians that this un-credentialed young biologist was dabbling in healing.

In the early 1960s, Naessens was twice brought before the bar. He was fined heavily, his Paris laboratory sealed, and much of his equipment confiscated.

He tried to start again on the island of Corsica, but Corsica was still France. Patients began again to seek him out and the authorities were soon after him. Naessens decided that he had to pursue his work far
from France, in a place he believed to be more open-minded. He left Corsica for Canada in 1964, carrying only a few key components of his microscope with him.

Unable to obtain any funding to pursue his research, Naessens began life as an immigrant by working day in an electronics repair shop in Oka, Quebec. The nights and the weekends were reserved for refining his somatoscope. Through some work he did repairing scientific equipment for several Quebec Universities, he got what seemed to be his first break.

A senior professor at the University of Sherbrooke hired him as a consultant on microscopy with a Nation Research Council grant of $25,000. But soon word got around the university of Naessens' trouble with the medical authorities in France, and overnight the grant and Naessens' opportunity were gone.

It wasn't until 1971 that he could begin again as a medical researcher. A friend introduced him to David Stewart, scion of a tobacco fortune and head of the McDonald Stewart Foundation, which had funded unorthodox cancer research for many years.

After losing a dear friend to cancer, Stewart had vowed to pursue an avenue that might lead to a cure, and he was decreasingly confident of the conventional approaches the foundation supported. He agreed to finance Naessens' research personally, and established a laboratory for him on the Mcdonald Tobacco Company's premises in Montreal.

Naessens' run-ins with the French medical authorities, however, had forever branded him as a quack his name was on the Quebec Medical Corporation's blacklist.

His new laboratory infuriated the orthodox oncologists under Stewart's wing, and they complained bitterly to the philanthropist. Stewart's response was to advise Naessens to move his research to some low-key spot and avoid getting embroiled in any more controversy.

Engaged by now to Francoise Bonin Sdicu, a divorced lab technician with four children, Naessens took over her family's summer cottage in Rock Forest, on the banks of the Magog river new Sherbrooke. He winterized and refurbished the place and built a lab in the basement.

Stewart's next concern was to get independent validation of the somatid theory and of the latest of Naessen's immune-system boosters, 714X this was the nontoxic camphor-based medicinal designed to be injected by way of a lymphatic node in the groin, that was to figure in his trial in 1989.

Naessens had come to the conclusion - not essentially disputed by the orthodoxy - that cancer cells needed nitrogen to survive and "stole" this nitrogen from healthy cells.

Discovering that camphor had a natural, if inexplicable affinity for cancer cells, Naessens' biochemically linked a molecule of nitrogen to one of camphor, aiming to force-feed the rouge cells - which would leave the immune system free to rebuild itself and fight the cancer.

Excited by the potential of 714-X, David Stewart approached McMaster University Medical Centre in Hamilton, offering to fund an investigative research project into Naessen's theory of the somatid cycle and the potential of 714-X as an immune-system booster.

The initial meeting at McMaster in March, 1972, went well. The university was represented by Peter Dent, then chairman of the pediatrics department and consultant in immunology to the Ontario Cancer Foundation. But of all of those present to hear Naessens, the most impressed was a young assistant professor of pathology and surgery named Daniel Perey, who volunteered to head the proposed investigation.

"The scope and the 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."

Perey's first visit to Naessens lasted eleven days and was by all accounts a revelation to him he saw through the somatoscope a new world to be explored.

The next time he brought Dent with him, assuming that his excitement would be shared. But Dent was clearly not happy to look through a microscope and see something that contradicted the definitions of disease he'd learned in medical school.

On returning to Hamilton, he wrote to the National Cancer Institute of Canada requesting its opinion of Naessens and his work. The institute sent him a page taken from a longer report it had published called Unproven Methods of Cancer Treatment. The page concentrated on an account of Naessens' trial in France and subsequent fine levied. This curt dismissal of Naessens' work confirmed Dent's unease.

But it was still Perey, not Dent who was conducting the investigation, and his enthusiasm for the somatid theory remained undiminished. Over the course of several visits to Rock Forest, Perey observed each of the forms in the somatid cycle proliferating and their apparent relation to cancer and other serious stresses on the body.

He recommended that Stewart's foundation purchase specialized photographic equipment enabling Naessens to capture these marvels on film - which was done. But the most telling sign of Perey's commitment to Naessens' work was a letter he wrote to support Naessens' application for landed-immigration status in September, 1972.

Emphasizing to the government the need for new and imaginative approaches to the search for a cancer cure, Perey extolled Naessens' contributions to the field, ending: "The scope and the 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."

Apart from helping to secure landed status for Naessens, this letter - a solid endorsement signed by an orthodox medical researcher - augured well for the future. Or so one would think.

Just over two years later, Perey wrote another letter to Naessens, enclosing with it a copy of his final report to the Mcdonald Stewart Foundation. The report rejected the somatid theory and Naessens' notion of bolstering the immune system to fight cancer.

Even so, Perey tried to reassure Naessens that the report was not a condemnation of his work, rather, he wrote, "We have come to different conclusions and interpretations based on the scientific evidence which we have gathered, although in many instances we have observed identical or similar phenomena as you have." What happened to change Perey's mind?

Late in 1972, Perey had been assigned other duties that effectively ate up the time needed to run the Naessens study. The day-to-day running of the project was passed on to a husband-and-wife team of researchers who were not in the least interested in proving the overarching theories Naessens has sketched. They were interested only in one large form of the somatid cycle that had been described as bacterium by German researchers who had isolated it in the 1930's.

The couple wished to study claims that this particular form had an effect on rheumatism. So although all future reports to the foundation on the Naessens project were still signed by Perey, their content was now a product of the new researchers, who did not accept Naessens explanation for what they observed in live blood through the somatoscope. They dismissed the stage of the somatid cycle as "artifacts" produced by mistake during the process required to observe them.

Perey, caught between two camps, wrote to Stewart that "microbiological dogmas are so entrenched in the couple's minds that they do not allow themselves the luxury of challenging them." More than that, however, he could not give.

After the McMaster stonewall, Naessens grew skeptical about the chances of the medical establishment's ever confirming his views - though his hopes rose briefly again in 1974 after Dr. Raymond Brown, a consultant for New York's Memorial Sloan Kettering Cancer Center, visited Rock Forest.

Brown sent a memo to the centre's director and to staff about Naessens: "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 confirmatory, this man should be brought to New York and given unlimited support and facilities to continue his research."

Dr. Brown returned to Rock Forest with an oncologist and a microscopist from Sloan-Kettering the three eventually drafted and signed a second and longer memorandum that reiterated the first.

These two memos generated much excitement among the hierarchy at the celebrated centre until someone noticed that Naessens' name appeared on the American Cancer Society blacklist. Immediately the memorandums were repudiated, the concerns of cancer bureaucrats outweighing the first-hand observations of expert scientists.

In 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, 714-X into cancerous and noncancerous rats.

He found that the compound had no effect on the rodents' tumors, and his results were reported in the Mcdonald Stewart Foundation literature in 1982.

But Jasmin had refused to follow Naessens' protocol for use of the drug. He had injected the medicinal into the tumors themselves rather than the lymphatic system, a procedure he has decided was impossible. Jasmin had treated 714-X as if it were a standard anticancer drug that essentially poisons either the cancer of the patient.

Naessen's whole terrain approach was designed to treat the symptom via the cause - the diametrical opposite of orthodox oncological approaches.

And so Naessens' reputation continued to be vilified among the cancer researchers - which may have served only to recommend him to the desperate underground of cancer patients. Through the 1970's and 1980's more and more people flocked to his knowledge hoping for a personal miracle.

Through the 1970s and 1980s, more and more people flocked to Rock Forest, hoping for a personal miracle. And doctors began to come, eager to learn more about Naessen's new biology. Fully aware of the penalties for practicing medicine without a license, Naessens was not capable of turning away anyone who needed help. The suffering were taught to inject themselves with 714-X, or referred to doctors who were willing.

All this action was not lost on Augustin Roy, the head of the Quebec Medical Corporation. In his eyes Naessens had been a marked man the moment he had arrived from France David Stewart's patronage had angered Roy but had also caused him to proceed with caution. In 1984 Stewart died suddenly.

On December 13 of that Year, the police and officers of the Quebec Medical Corporation raided Naessens' house and laboratory, seizing vials of 714-X and some 150 medical files that would bring Naessens to trial in the Sherbrooke courthouse in 1989. He seemed doomed to the hinterlands of science.

I first traveled to Rock Forest in January, 1992, taking with me a friend who would be termed a high risk for cancer: His mother and one brother have died from the disease his father and another brother are currently undergoing treatment for it.

An unlikely spot for a revolution in science, from the outside Naessens' laboratory looked like any other summer cottage. At -18° C, however, it was not summer, and the snow crunched and squeaked as we walked towards the second of two cottages in the compound.

An informal seminar for two American MDs was being held that day, and we were invited to attend. Two guard puppies yelped, and tried to lick our faces, as Daniel Sdicu, one of Naessens' four stepchildren, opened the door.

Inside in a room bare but for a long table and chairs, Naessens stood to greet us. Tall and imposing -- even his stepchildren refer to him as "Monsieur Naessens" -- he was formally polite. Introduced to the two doctors from Vermont, we sat quietly and listened.

One of the doctors, Bradford Weeks, interpreted Naessens' French for the other, a gaunt, worried-looking man. Part of the discussions in progress involved a new modified version of the somatoscope that Naessens calls an "ultramicroscopic condenser," which -- attached to any optical microscope and for a modest $3,000 -- will enable a doctor or scientist to perform basic aspects of blood analysis according to the somatid theory. The rest covered what was to me by now familiar ground, with Naessens acting the strict but fair teacher.

Then we crunched fifty yards through the snow to the older, main cottage. Inside this neat and tiny house -- clearly Naessens' home -- we removed our boots, were given woolen slippers to wear, and were shown into a sitting room whose most prominent feature was an illuminated shrine to the Virgin Mary.

In one corner of this otherwise ordinary room a staircase led down. At the foot was a real if somewhat antique laboratory: Test tubes, retorts, specimen tubes, the lot. To one side, dominating everything, was the somatoscope. Looking like a cross between an ordinary large optical microscope and the inside of an old television set, the revolution in microscopy was definitely complicated.

A metal box labeled Helium-Neon Laser was attached to one side and a small video camera to the top a web of wires ran to other contraptions below and behind it there was a computer to the left, and some high-tech electronics connected to a monitor and Super VHS machine on the right.

Wandering down the long narrow room, with its panoramic views of the Magog ice scape, I came across a strange fleshy pink blob under clear viscous liquid in a sealed jar, like something left over from a David Cronenberg movie.

I asked the worried-looking Vermont doctor what it was. He peered closely at the slimy bolus and eventually replied, "I don't know, but whatever it is it's alive." Naessens cheerfully explained that the blob had started life as a bit of muscle tissue he'd taken from a living rat, injected with a concentration of pure rat somatids, sealed in a sterilized glass jar under vacuum, and then put on his lab windowsill back in 1978. "Ever since," he added, "the cells have continued to grow." "Great," the doctor laughed uneasily. "Grow your own hamburger."

What everyone was really here for, however, was to see his own blood under the unique microscope. First taking a sample from Dr. Weeks -- washing his hands, sterilizing the doctor's finger with alcohol, then taking the crimson pinprick onto a slide and covering it with a sliver of glass -- Naessens moved to his extraordinary device, flipping switches, positioning the slide, peering through the eyepieces.

After focusing, he flipped another switch and the nearby monitor suddenly revealed what he was seeing. Tiny star-like dots pulsed and danced around brilliant circles that were, the biologist explained, red corpuscles. An awed silence followed, then gasps of amazement -- there was a singular beauty to this spectacle.

Carefully shifting the slide around -- the tiny pinprick of blood at 20,000 X like a hot tub full of stars -- Naessens explained the various forms we saw in normal and healthy living blood, untreated, unstained.

Then it was the worried doctor's turn. There was the wait as the slide was prepared. But this time the blood looked distinctly different: The level of pulsing somatids seemed greatly reduced, and the later forms of the sixteen-stage cycle were clearly present, some great twisted shapes, bars, and curious blobs with filaments.

"This is so strange," the doctor murmured, "seeing your own blood. I mean your own blood alive." Naessens scanned the sample more thoroughly than he had Dr. Week's. He asked if the doctor had been suffering from fatigue (he had) and the doctor in turn asked a few questions about AIDS that seemed to indicate the source of his worry.

Avoiding any explicit diagnosis, Naessens told him that there was definitely a stress on his immune system and that he should cut down his workload, rest more, and put himself on a strict diet -- no red meat, no dairy products, lots of fresh fruit and vegetables. Then get his blood checked again in a month or so.

The man's mounting gloom was contagious it also seemed a rather private moment to have strangers present, so my friend and I left, arranging to come back the next day. Neither of us could shake the image of that doctor faced with a picture of his mortality.

The next day it was my blood Naessens looked at first. With sweaty palms and a knotted heart, I waited until the video monitor was flipped on, seeing that universe of stars and red corpuscles like jostling balloons. Naessens moved the slide, pointing out forms, each one of which had me asking if that meant cancer.

But no, all was as it should be. Beyond an apparent indication of iron deficiency Naessens saw nothing amiss. Once I was able to relax, there was something inexpressibly thrilling about the play of the elements in living blood my blood -- something fundamental.

But the mood was shattered. My friend's blood appeared next on the monitor. The red corpuscles seemed more frail, less defined. And stretching across the screen, coiled and serpent-like, was the last form in the sixteen-stage cycle -- the "thallus," the discarded shell that has expelled new somatids. As Naessens moved the slide, indicating other forms from the complete cycle, my friend paced the lab in shock and fear.

Naessens continued to scan, pointing out forms, one of which -- a circular shape with waving snake-like protrusions that he termed the Medusa head -- seemed busy surrounding "intruders" or seemed at least very busy. "Ask your most eminent hematologists what that is ," Naessens told me. "They cannot answer."

When my friend emerged from a prolonged and silent spell in the washroom, Naessens assured him that all this activity showed that his immune system was fighting, certainly, but in good shape. The somatid level was still relatively high, and the presence of the Medusa heads indicated an aggressive response to some form of stress.

My friend then told Naessens his family history, but the biologist still resisted any diagnosis, and advised him to follow the same regiment of diet and relaxation he'd recommended for the doctor the day before.

Augustin Roy had accused Naessens of furtive and covert work but Naessens was hardly secretive, his lab and files patently open to anyone who was interested. No-one was getting rich here either. When I asked if he's supplied 714-X free to anyone willing to perform standard animal tests he immediately said yes, providing the tests were carried out according to his protocols, the compound injected intralymphatically and not into the tumors or the blood.

In Canada, because of his problems, Naessens was giving it away to any physician who asked for it through official channels. As of October, 1992, 210 MDs across the country were administering it to patients, admittedly on compassionate grounds, in most cases, and at their patients' request.

In retrospect, what impressed me most during this first exploratory visit was the devotion of Naessens' stepchildren. Only in Rock Forest did I learn that their mother, Francoise, had died of a rare fungal infection just four months earlier.

(It was one of those horrible ironies that Naessens, who had helped so many people in endgame situations, had been unable to help his wife.) Her children's faith in their late mother's strange and brilliant husband seemed absolute. That two of his stepchildren had degrees in biology said more for Naessens than any other fact of his life.

Shortly after we left, my friend's anxiety gave way to rage. How could I have subjected him to this? How could Naessens be so irresponsible as to put anyone through such an ordeal? Before we drove home we went back to Naessens again, who went out of his way to reassure my friend that the apparent stress affecting his bodily system could easily be corrected at such an early stage. Hearing, once again, about the diet he should follow, my friend just groaned, "But what's left to eat?"

Never did a man follow a diet so religiously as did my friend over the next three months. And what I did, almost as religiously, was take the video tape of our blood and a description of Naessens' theories to anyone I thought might help me judge them.

Calling Tak Mak, head of cellular and molecular biology at the Ontario Cancer Institute, and one of this country's most eminent cancer researchers, I was surprised to find him unwilling even to hear an account of Naessens' work. "It doesn't sound kosher," was all he said, adding that blood wasn't really his field anyway.

He referred me to a leading hematologist at the OCI, Dr. Mark Minden, who reluctantly agreed to meet me and view the video tape shot through the somatoscope. Arriving early, I found Minden rummaging around his tiny cluttered office in jeans and sneakers. He claimed to have forgotten the appointment he then left the room on the lookout, he said, for a VCR.

He came back half an hour later, without the equipment and patently hoping that I'd be gone. Instead I suggested that the nation's finest cancer-research hospital might have an audiovisual department. Muttering about grant applications that needed his urgent attention, he finally led me up many stairs and down many corridors to a cupboard possessing a monitor and a VCR into which I plugged my tape.

"What were the somatids?", I asked. "Platelets or proteins in Brownian motion", he replied, but I could see that something on the tape fascinated him. Did he ever study live blood? No -- or very rarely -- was the answer. The electron microscopes and ordinary optical microscopes he used required fixed and stained blood.

To prevent his running out of the cupboard -- he hopped from foot to foot like an athlete about to make the hundred -yard dash -- I fast-forwarded to my friend's blood, asking him about the difference between the samples. Well, he said, this blood was obviously in an advanced state of clotting.

When I assured him that the sample had been taken under the same circumstances as my own, he pointed out that blood clots at different rates, though he'd have to look at it under the electron microscope to be sure of what he was seeing. What were the large coiled forms that Naessens identified as the final stage in the somatid cycle? Fibron, he said, a protein that forms when blood begins to clot. Why was there none of it in my blood sample, even after ten minutes of watching? He had no answer to that.

What Minden couldn't attribute to clotting he called "artifacts" -- a scientific way of saying "bits of stuff." The term in microscopy also implies structures that are accidentally created in the human handling of the sample on the slide. We looked at the Medusa head -- the form Naessens had told me to show to a top hematologist.

He would have to stain and fix it to see if it had a nucleus, before he could comment it was the only artifact that seemed to shake his certainty. I then showed him a diagram of Naessens' somatid cycle, which he dismissed outright. As I left Minden I thought, well, at least when pushed into a closet he was willing to look.]

It took a while to find a doctor with an orthodox scientific background who was willing to stand up for Naessens. Dr. Dietmar Schildwaechter is an MD and medical Ph.D. who was a longtime faculty member of the University of Pennsylvania School of Medicine, the oldest medical school in the U.S.

One of his special fields was early cancer detection he left the university to take over the Ratzenburg Klinik fur medizinische Rehabilitation, one of the world's most advanced cancer-rehabilitation centres, in his homeland, Germany. He now operates an office in the District of Columbia consulting in preventive medicine and oncology while continuing to care for patients in Europe.

Schildwaechter came across Gaston Naessens in 1990 after discovering they were both treating the same "celebrity" patient, a "relative of George Bush". In 1986 the woman was diagnosed with "one of the most devastating cancers: an oat-cell carcinoma of the lung that had metastasized to the brain, the adrenal gland, and the tissue between the lungs," says Schildwaechter.

She and her husband had investigated the available treatments and discovered that for such a cancer there was no statistical survival after three years, though the rare individual did survive. Electing to go to the leading clinic in Bonn, she received chemotherapy, radiation, and various other primary treatments that brought the disease under control.

Then she was referred to Schildwaechter, who kept her on a maintenance program, employing frequent cancer and immune-system profile tests developed by Dr. Emile Schandl, a Hungarian-born research biochemist and geneticist who lives in Florida.

The monitoring-test results - immune parameters, complete blood count, differential count, blood chemistry, and so on - were computerized, giving, over the years, some of the most exact documentation of the results of the treatment of this illness that exist. "At the end of 1989," Schildwaechter says, "her blood sample arrived and its values had changed remarkably.

The immune-system values had improved drastically. We had always seen a slight activity from her cancer - which we'd kept in remission - now it was down to zero. There were also two other markers that could not be done during this testing because, as our lab said, of something like chemical interference in her metabolism."

Schildwaechter called the couple to find out if something had been going on and found out that they had visited Naessens in Quebec, where the man had been taught how to give his wife injections of 714-X. "They did not want to tell me because they thought I might not approve." They needn't have worried.

Schildwaechter finally met Naessens at a seminar held at Sherbrooke in 1991, and he unreservedly accepted Naessen's theory. At medical school in Europe he'd learned about Bechamp and others "basically excluded from medical schools over here. We were prepared for something like this," he says. "I knew there was something in the blood we'd not been able to diagnose, and I realized that Naessens had discovered and identified what others had only partially seen."

The resistance to Naessen's work from orthodox practitioners was only to be expected. Schildwaechter himself had been "a totally orthodox, tunnel-vision MD who didn't want to look at anything out of the mainstream" when he had been at the University of Pennsylvania. But then as he practiced he had begun to feel increasingly frustrated with the limits of his profession: "I had the most modern hospital, I could purchase the best equipment, yet I was still unable to monitor what I wanted."

In his spare time Schildwaechter traveled the world visiting medical centres and studying their techniques for monitoring blood, finding that none of them, from Britain to the Philippines, had the specificity and sensitivity that he required. "I could not in all conscience tell my patients that they were free of cancer after a monitoring test that was only sixty-five-per-cent accurate."

Then he met Schandl and, in a sense, defected from regular medicine: "Colleagues I had worked with for years were not even willing to discuss this stuff, even though Schandl was a leading biochemist and his test results were couched in all the proper forms." In Schildwaechter's view, his colleagues' excuse for dismissing Schandl's testing was that it was too complicated and impractical for ordinary labs to achieve.

The real reason, he believes, was that Schandl's tests could document the workings of alternative therapies that regular medicine had long dismissed and violently resisted.

The future of medicine in Schildwaechter's eyes lies in prevention, and the essence of prevention is a greater understanding of the workings of the immune system and the development of methods to detect telltale signs of imbalance long before symptoms appear. Combining, as he now can do, Schandl's tests with Naessen's somatoscopic monitoring, and something known as cell-milieu medicine - which determines the patient's exact needs for trace elements, amino acids, and vitamins.

Schildwaechter claims tremendous success with his German practice in detecting and correcting imbalances that would lead to degenerative diseases. (He hesitates to practice in the U.S. for fear of Naessens-style prosecutions.) "Cancer," he announced with absolute conviction, "has become a truly preventable disease if we would only employ these blood tests.

"The number-one cancer today is breast cancer, so we tell women to have mammograms after forty. But regardless of how modern the equipment, there is still a high false-negative ratio and by the time the mammogram detects something, we've lost two years during which we could have prevented the cancer if the somatoscopic blood tests had been used."

Naessen's day is coming, insists Schildwaechter: "A number of oncologists are impressed with his work, even if they won't admit it at the moment." He sighs, and adds, "Szent-Gyorgyi, the discoverer of ascorbic acid and one of the great Novel laureates, remarked that whenever you pioneer something you first have to realize you may be called a quack. But the Establishment will check you out, and if they find your discovery useful it will be accepted through the 'back door' - certainly without giving credit to the pioneer."

After three months' effort I did find two cautiously curious souls who were willing to look at the material through the back door and very much off the record. Even more off the record, they described Naessen's work as interesting, but hesitated about coming to Rock Forest with me to see the somatoscope in action.

Finally I found a young microbiologist, Jacqueline Conant, then working as an associate scientist with the Robert Wood Johnson Pharmaceutical Research Institute in Toronto, who was intrigued (and professionally brave) enough to make the trip with me - and one very nervous friend heading for his second appointment with his own blood.

The moment Naessens had drawn the blood in question and turned to slide it into the jaws of the somatoscope, that friend was heading up the stairs. Naessens flipped on the monitor, revealing a vastly improved picture. He laughed and shouted, "C'est meilleur!" calling my friend back.

The full cycle of somatids was no longer evident, and the red corpuscles seemed more defined, more robust. The fast-clotting blood, as Dr. Minden had described it, had changed its nature in three months.

Next, Naessens showed us a video tape of blood from a patient with very advanced cancer. If normal blood had a sparkling beauty to it, this murky broth of filaments and tendrils had something deeply depressing about it. All the sixteen stages in the somatidian pleomorphic cycle were clearly visible, floating like wreckage in the blood. I couldn't see anything resembling red corpuscles and asked Naessens if this were so. He pointed them out - bubbles filled with grit, their edges jagged filaments.

Then Naessens played a tape of the same patient's blood after three months' treatment with 714-X after six months and a year. The progress was clear and dramatic. From what looked like Kitts's last cough, the final tape revealed that bright dancing universe I'd come to recognize as life and health. My friend was cheered, more at seeing what diabolically cancerous blood looked like than at this unknown patient's restoration to health.

Jacqueline Conant had looked at everything with obvious fascination, asking many questions in tolerable French, but it was only on the way back home that I was able to find out what had been going on in her mind.

"It was like entering the last century going down there," she said. "It reminded me of Banting and Best's lab at the U. of T. Then in the middle of it all, there's this feat of high-tech engineering through which he is able to make some truly remarkable observations." But what did she think he was seeing?

"It's never been possible to see these particular entities before - and I call them entities because they do appear to be living. What's their nature?" she asked. "They could possibly be fragments of genetic material, all right, but what exactly is their biochemical structure?"

One of the things Naessens had shown her was an electron-microscope photograph of a sectioned somatid taken at 140,000 X it resembled something Norval Morrisseau could have painted. "I've never seen anything like it," she said, choosing her words with great care. "I certainly didn't recognize it to be of viral origin. It had definite structure, not structure as we normally know it, with a nucleus. But, there was definite order to this particular structure."

Could it be, as Naessens maintained, a precursor to DNA?

After a long silence, Conant replied, "It is conceivable. It's the particular building blocks of DNA that one has never yet been able to visualize. In the electron microscope we've seen certain genetic fragments, chromosomes - the structures are fairly well elucidated."

A mighty pause. "I have trouble with that term precursor, but I suppose, yes, it is conceivable." Then, with passion: "There are so many tools around today that we would be able to elucidate a lot of Naessen's work, and yet the exciting thing for me is the extraordinary power of that particular microscope."

For microbiologists such as herself, she said, "it would certainly permit better patient management and therapeutic monitoring. There are really all kinds of exciting applications for such a device both diagnostically and academically."

She paused again, and frowned thoughtfully. "He was certainly able to show that many of the various examples of forms in the blood are quite disease-specific." Naessens had shown her still photographs of somatid forms in the blood of AIDS, cancer, and multiple-sclerosis patients.

I told her Dr. Minden had described most of the forms as artifacts, and asked if the term did mean "bits of stuff." She laughed and said it did. But where did the stuff come from, I wondered, and why was there such a regular pattern in its forms? Could it all be the result of human handling of the samples?

She looked at me, gauging how far she wanted to go in her answer, and then, apparently, decided to jump: "There was very little manipulation between taking the blood, making the slide, and then viewing it. That's why there has to be something in it, and it certainly warrants further study. But it's so foreign to the accepted dogma, you know, that it's going to be a hard sell."

Perhaps Naessens will live long enough to see a front-door vindication of his life's work. In 1990, after receiving the positive results of non toxicity tests, Health and Welfare Canada agreed that 714-X could be supplied by Naessens to doctors whose patients were suffering from terminal cancer. Doctors have to apply to Ottawa, where authorities may try to talk them out of using it, but such requests now cannot be refused.

Naessen's frustration lies in not having approval for the medicinal's use in the early or precancerous stages of the disease, where he thinks it might be of the most use. But even with terminal patients he has begun receiving reports indicating that 714-X helps relieve pain and restore energy during a patient's final days or weeks.

As far as his troubles with the Quebec medical authorities go, they've resulted in a temporary draw. Naessens and his lawyer, Conrad Chapdelaine, decided to fight back against the eighty-two counts that were laid after his first trial.

They countersued, issuing subpoenas to Augustin Roy, among others. The medical college replied with a plea-bargain offer, and in the end dropped seventy-two of the counts and reduced Naessen's fine to $5,000. Naessens and his lawyer regarded the outcome as a technical victory, and so far there have been no more initiatives on the part of the authorities.

There is also growing interest in Naessen's approach to AIDS he was invited to the controversial conference on alternative treatments held in Amsterdam last May - also attended by Luc Montagnier, the French scientist credited with discovery of HIV.

In Europe, the Philippines, New Zealand, and Australia, physicians are using 714-X, and researchers, covertly and overtly, are investigating his work. Daily, results come in - favorable and unfavorable - the conclusion being that 714-X does work most effectively when the immune system has not been totally wrecked by disease.

This has always been Naessens's contention. And as the new biology and the new medicine emerge, the textbooks will be rewritten, as they always have been, this time the emphasis shifting from cure to prevention.

An eminent Canadian oncologist (whom I will do the courtesy of not naming) has recently agreed, after visiting Rock Forest at my suggestion, to supervise certain tests to validate Naessens's somatid theory, an action that could jeopardize his career if publicized.

In the U.S., and independent study on 714-X using human patients, sponsored by Charles Pixley, from Rochester, N.Y., has been under way since January of 1992.

In the Eastern Townships the man who may well be recognized one day as a Galileo or an Einstein continues the work he has devoted half a century to, seemingly unconcerned by the fuss, the orthodox hostility. He works in silence and concentration in his laboratory, its windows on the Magog showing a landscape scarcely changed since the glaciers retreated.

Others have begun to praise him, but he himself might be content to live by a line from Paracelsus: "I pleased nobody except the people I cured."