Ian & Stuart's Australian Mac: Not for Sale/Another.not.for.sale (Australia).iso/wide open road/sumeria/Science/naessens.txt

Text File | 1994-06-30 | 14KB | 270 lines

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)
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 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 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: [phone]