RIFE
RESEARCH AND ENERGY MEDICINE:
A PHYSICIST’S VIEW OF DR. RIFE’S NON-DRUG AND NON-SURGICAL
TREATMENT AND CURE OF MICROBIAL ASSOCIATED DISEASES
by Gary Wade
(This
is a revised and updated version of an article, which was originally released
in the
August 1994 issue of Health Freedom News.)
Rife Energy
Medicine---During the 1920’s and 30’s, Dr. Royal Raymond Rife produced some
rather astounding accomplishments in medicine and biology. First, he invented a
new kind of optical microscope. This microscope could be used to observe
viruses in live cells and tissue culture. (see Addendum A on Resources page)
Rife built five of these microscopes. Rife never published the plans to his
microscope and to this day those in the scientific establishment not familiar
with Rife’s work wrongly claim that it is generally impossible to see or
identify a virus with any optical microscope (see Rife microscope addendum).
Rife’s second
great accomplishment was to invent a variable frequency flashing light
ultrasound source which could kill bacteria, rickettsias, protozoa, fungi, and
viruses. By 1939, Dr. Rife had both identified the microbes and light flashing
rates ( ultrasound frequencies ) required to kill these microbes, which
were associated with fifty-two major diseases, including carcinoma and sarcoma
cancers.
In this
article we will describe what Rife’s frequency instrument was and how it could
destroy a microbe without harming the host / patient.
Figure 1
shows a schematic view of the Rife frequency instrument in operation treating a
patient. The frequency instrument consisted of an old style X-ray tube, which
had been back filled with helium and or argon gas at very low pressure and had
a current flow through the tube driven by a packetted sine and or square wave
voltage oscillations as depicted in Figure 2. Each time the plate-anode voltage
polarities reverse as depicted in Figure 2,
there is an associated current surge reversal and shock wave generation in the
tube gas. The shock wave travels to the tube wall and vibrates it producing
sound / ultrasound in the air at the tube outer surface. The electron current
collides with the tube gas optically exciting and ionizing the gas atoms. The
instantaneous light intensity output of the tube is approximately proportional
to the instantaneous tube current plotted in Figure 3.
Therefore, the plot of the light intensity from the tube gas discharge verses
time will have the same shape as that of Figure 3. Note that every other
current and or light pulse has a different peak amplitude. This difference in
current / light intensity amplitude is do to the preferential electron current
flow from the hot tungsten cathode to the metal plate anode. The hot cathode
when at a negative polarity (voltage) relative to the anode readily emits
electrons for acceleration across the tube. However, when the "anode"
is at a negative voltage relative to the hot tungsten cathode, the electron
current across the tube must build up from electrons released by positive ions
colliding with the plate, electrons emitted by the plate from photo-emission
caused by ultraviolet light from meta-stable atoms, and accelerated electrons
colliding with atoms and freeing new electrons to join the current flow. (For a
non-technical explanation of this and information on the practical rife device
please see;
NON-TECHNICAL
OVERVIEWor WHAT MAKES THIS
RIFE MACHINE DIFFERENT).
Note
that there are two shock wave pulses per single electrical oscillation cycle. Also,
note there are two light pulses per single electrical oscillation. In other
words there is a frequency doubling effect, i.e. a one million cycle per second
sine wave voltage across the Rife tube will produce ultrasound with strong
components at two million cycles per second. As a practical example, Rife found
that the common carcinoma breast cancer of his time, (which is now reaching
epidemic proportions among women), was killed by packetted sine and or square
wave voltages in the Rife tube of a frequency of 11,780,000 cycles per second.
This means light flashing rates and ultrasound of 23,560,000 cycles per second
will be produced by Rife’s tube.
For the
currently trained biologist and medical researcher, all of the above statements
about Rife’s work and accomplishments are suspect at best. The reason for this
is that they have a very limited knowledge of physics and no knowledge of
Rife’s research results. For example, they do not know that Rife isolated a
viral sized, spore like, motile form of the E-coli bacteria that when exposed
to prolonged ultraviolet light became a virulent carcinogen, which invariably
caused carcinoma cancer when injected into lab animals. The key to getting
Rife’s work and accomplishments into general medical and biological use is an
end to this ignorance about how and why Rife’s frequency instrument worked to
kill microbes.
To that end
I will now describe and illustrate how the Rife frequency instrument can
destroy a virus. I will illustrate how a specific virus can be destroyed by a
specific frequency of ultrasound. This ultrasound is generated by the Rife
frequency instrument by three methods. In the first method, note that light
carries linear momentum and that when the pulse of light from the Rife
frequency instrument is absorbed and or reflected by the patient’s skin layer
that skin layer must recoil in the direction of light flow from the tube to
conserve linear momentum. When the light pulse has ended, the skin relaxes back
toward its non-light pulse exposure position. In other words, periodic light
pulses generate periodic pressure pulses in the patient’s skin layer, which
travel into the patient’s body. The Rife frequency instrument converts the
patient’s entire exposed skin surface into an ultrasound transducer for the generation
of ultrasound. Even though the efficiency of ultrasound production is
exceedingly low by this method, it is still adequate to kill microbes, because
we are dealing here with a resonance phenomenon. In the second method, the
plasma shock waves inside the Rife tube vibrate the tube wall causing
generation of ultrasound in the air. This ultrasound travels to and enters the
patient. In the third method, the oscillating electric fields from the Rife
tube travel out into the room and interact with (vibrate) the charged ions in
the patient’s body. These vibrating ions generate ultrasound in the patient of
the same frequency as the electric field vibration rate of the Rife ray tube
(no frequency doubling effect).
As a
practical example, Rife would treat his cancer patients using his
frequency instrument for three minutes of exposure once every three days.
Usually his "terminally" ill cancer patients would be cancer free in
about thirty such treatments or less, as was verified in the 1934, 1935, and
1937 test clinical trials carried out by the U.S.C. Medical School Special
Medical Research Committee. That same committee then suppressed the research
results.
The reason for
the short three-minute treatment is to kill off only a thin outer layer of
cancer tumor tissue at one time. This allows the body’s immune system to remove
this layer before the next treatment. The entire cancer tumor could have been
killed / destroyed in a single Rife frequency instrument treatment of perhaps
one to one and a half hours. However, then the cancer patient would have a
large mass or masses of dead cancer tissue in them, which would become a feast
for a massive bacterial infection. This bacterial infection could lead to liver
and kidney damage and general toxemia.
The Rife
frequency instrument killed the "normal" carcinoma cancer cell of
Rife’s time by rupturing the thousands of BX cancer viruses they contain and
thereby dumping the BX cancer virus contents into the cancer cell cytoplasm.
This BX cancer virus as Rife named it in 1931 is not a virus by the normal
standard usage of the term virus today. Rife based his definition on the fact
that the BX cancer virus could pass through the finest Berkett porcelain filter
of the time (000 filter). The BX cancer virus is ovoid in shape, .066 microns
along the major axis and .05 microns along the minor axis. It is motile, driven
by a proton transport flagella the same as its bacterial parent, the E-coli
bacteria. When this BX cancer virus is ruptured it spills out its gnome,
ribosomes, RNA, enzymes, and various proteins. When thousands of these ruptures
occur all at once in a carcinoma cancer cell the results are fatal to the
cancer cell. A similar situation occurs in the sarcoma cancer cell when the BY
cancer viruses are all disintegrated at once, The BY cancer virus is another
form of the BX cancer virus which Rife found caused sarcoma cancer after it had
been exposed to prolonged ultraviolet light exposure.
To see how the
ultrasound generated by the Rife frequency instrument can destroy a virus we
will examine the outer protein coat (capsid) structure of a virus. Most viruses
of interest which cause disease in plants and animals have an icosahedral
capsid structure as illustrated in Figure 4A and B.
A specific example of this icosahedral capsid structure is illustrated in Figure 5.
Each dark circle represents a spherical protein molecule clump. When the virus
capsid of Figure 5 is folded together as indicated in Figure 4A and B, a simple
virus capsid model has been formed. Examination of this capsid model shows a
large number of intersecting and overlapping closed rings of protein molecule
clumps. These closed rings of periodically spaced protein clumps are
illustrated in Figure
6A and B. In classical physics when studying standing wave
phenomenon the periodically spaced protein clumps, as illustrated in Figure 6A
and B, are known as the mass beads on a string with circular boundary
conditions problem. Figures 7A, B and
C, illustrated this classical physics problem.Figures 8A, B, C,
and D illustrate some of the standing wave motion modes
which the closed periodically spaced protein clump rings of Figure 6A can
sustain. Figure 8A shows a ten member protein clump ring linearized for ease of
graphing wave motion displacement of the center of the protein clumps from
their equilibrium position. Figure 8B shows the most stressful oscillation mode
for the ten member protein clump ring. In this oscillation mode, adjacent
protein molecule clumps are always going in opposite directions and therefore
putting maximum stress on where they are bonded together. If this oscillation
mode is raised to a high enough displacement amplitude the ring will rupture,
If enough rings are ruptured, the virus capsid disintegrates. The Rife
frequency instrument when set to the frequency which corresponds to the most
stressful oscillation mode for the virus of interest, as illustrated in Figure
8B, will destroy that virus capsid coat and therefore destroy the virus. The common
virus capsid coat was chosen to show how the Rife frequency instrument could
destroy a microbe which has closed on themselves periodically spaced protein
clump structures. Bacteria, protozoa, rickettsias, and fungi all have versions
of these closed on themselves periodically spaced protein clump structures, in
their structure, which makes them susceptible to destruction by the Rife
frequency instrument (specific frequency of ultrasound). Advancements
in electron technology have made it possible to obtain Rife frequency
instrument results (generation of specific frequencies of ultrasound) using
several different approaches. For example, electrodes applying a square wave
voltage to the bare skin, oscillating capacitively coupled high voltage discharges
through gas discharge tubes touching the bare skin, multi wave multipole
electromagnetic radiation devices, intense very rapidly changing (pulsed) in
strength magnet field devises, and a piezo-electric transducer driven by an
appropriate voltage signal source. In our present circumstances where
antibiotic resistant bacteria are about to become rampant, anti-viral drugs are
largely still just a bio-tech dream, and the war on cancer has been a dismal
failure for the cancer patient, but not for the so-called cancer researcher. It
is long since time for Rife's 1930,s work to be implemented. Final note:
When looking at Rife’s actual lab notebook for the mortal oscillation rate for
a particular microbe, you find a frequency and a wavelength listed for that microbe.
However, further examination of the notebook shows that the given frequency and
wavelength are not related to each other. In other words the product of the
wavelength times the frequency listed for various microbes does not give a
constant value for wave propagation. The logical conclusion is that Rife was
using two frequencies of electrical oscillation in his frequency instrument.
One frequency Rife gave directly and the other is implied by the wavelength
given, because when you have a wavelength you always have an associated
frequency from the fundamental relationship that wavelength multiplied by the
associated frequency equals wave propagation speed. When using two different
frequencies of electrical oscillations in an amplifier circuit which Rife used
in his frequency instrument, there are two obvious possibilities of what can be
done: 1) One oscillation frequency can be used to amplitude modulate the other,
and 2) The two oscillation frequencies can be added together and then
amplified. This article has assumed the first possibility. If I had assumed the
second possibility, then qualitatively the results would be the same except
that there would now be a new additional strong ultrasound frequency component
generated by the tube of a frequency equal to the difference between the two
frequencies Rife used. This situation is illustrated in Figures 9A
and B. I have attempted to verify the validity of this second possibility using
"known" mortal oscillation rates for specific microbes obtained from
correspondence between Rife and his associates. However, so far all my
calculated results are contradictory. Gary Wade is
currently the President of the American Institute of Rehabilitation and can be
reached e-mail at RifeTech E-Mail. IF YOU FOUND THIS ARTICLE OF REAL VALUE, PLEASE MAKE A HARD COPY WHILE STILL AVAILABLE.
REFERENCES: 1)
The New Microscopes, by R.E. Seidel, M.D. and M. Elizabeth Winter, Journal of
The Franklin Institute, Vol. 237, Feb. 1944. 2) What Has Become of the Rife
Microscope?, written by Christopher Bird, New Age Journal, March 1976. 3) The
Cancer Cure That Worked!, written by Barry Lynes. Published in Canada by Marcus
Books. 4) The Royal R. Rife Report, compiled by Alison Davidson, (see page 83),
Published by Borderland Sciences. .5) See lecture given by Gary Wade on
September 25, 1999 at the Rife Conference held in Edmonton, Alberta, Canada,
Title: Finding The Actual Ultrasound Frequencies To Kill A Microbe Under A
Microscope.
