The Amazing
Wonders of
Gaston Naessens
Gaston Naessens
Super-microscopes and
suppressed cancer treatments
| Nexus Magazine February--March 1994 | by Steven R. Elswick. Editor, Extraordinary Science |
HISTORICAL NOTES
THE MODERN UNIVERSAL MICROSCOPE
THEORY OF OPERATION
THE SOMATID CYCLE
714X
THE SECOND CHANCE
THE MODERN UNIVERSAL MICROSCOPE
THEORY OF OPERATION
THE SOMATID CYCLE
714X
THE SECOND CHANCE
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.
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 three 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)
organisations 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 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 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.
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 autolike 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 the
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 original 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-Bemard et Turenne, technical specialists and defence contractors
near Paris.
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° 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 upon each at 90° 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 rays before
being injected onto the specimen.
Two
light sources, the first (1) an incandescent one with a wavelength of about
3600 angstrom, the second (2) an ultraviolet one with a wavelength of about
2200 angstrom beat against each other to produce a third wavelength of which
passes through a monochromatic filter (3) to produce a monochromatic ray.
This ray is exposed to magnetic fields (4)-the Zeeman effect- that
divides tt to produce numerous parallel rays (5) that. In turn pass through
a Kerr-cell (6) that increases the frequency. It is this light
source, invisible to the naked eye, that strikes the specimen slides. The
Image is reconstituted by the microscope. Credit: Guide Resources
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 which do not use lenses, but rather
apertures which are smaller than the wavelength of light. One such
microscope engineered in Cornell University has achieved a resolution of 400
angstroms—a far cry from the 150 angstroms achieved by Naessens' 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 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 do not 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 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.
In a long
lost chapter of history in 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 dominate medical philosophy for the past century.
Now, a hundred years later,
Gaston Naessens has discovered an ultramicroscopic, 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, and had
a sixteen-stage life cycle. Only the first three stages of the somatid 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 reasons such 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 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 today which has embraced
Pasteur's germ theory wholeheartedly. Naessens' work is repeatable. The ability
to culture somatids is a bellwether to the rewriting of microbiology!
Naessens
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"
The research of Gaston Naessens
has culminated in the discovery of 714X—an enzyme which helps the immune system
to 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 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, "germs are not the cause of, 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 wipes out the immune system and
other bodily resources.)
The cancer death toll between
1970 and 1986 was approximately 6 MILLION. Sadly, the conventional treatments of
chemotherapy and radiation therapy are nothing more than slow death sentences
that enrich the cancer industry. Possible miracle cures are quickly quashed by
the FDA (Food & 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 & RESEARCH is one organisation working
closely with the FDA and the IRB (Institution Review Board) to do work with 714X
legally and ethically. 714X is an injected medication and must beprescribed by a
doctor.
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