Rife machines, John Crane A Study of

THE ROBERT CATHEY RESEARCH SOURCE

http://www.europa.com/~rsc
---------------------------------------------------------------------------
The following material was culled from John Crane's voluminous "A Study of
Electron Therapy" (According to the Copyright page: Library of Congress
Catalogue Card Number: 78-72588), and is apparently from Rife's book:
History of the Development of a Successful Treatment for Cancer, and Other
Virus, Bacteria and Fungi. It is not complete, as will become apparent. It
is also somewhat redundant, indicating that the parts I presume to be from
the book by Rife are different drafts, copied willy-nilly into Crane's
work. Indeed, it is suspected by several researchers that this is in
reality John Crane's writing, based on what Rife told him, and which Rife
merely signed as author. In any case its more information, and hopefully
Crane submitted a copy of the finished book to the Library of Congress, as
he undoubtedly applied for a copyright.

John Crane was an interesting man to my mind. I did not know him well, but
from my little experience with him, I found him to be a good and sincere
person. I carried on mostly telephonic communication with him over a period
of about 2 years. I finally met him shortly before he died, last year in
the Veterans Hospital in LaJoya, California, a little north of San Diego.
Amongst his last words to me were "We could accomplish so much if we all
worked together." I think Rife and John would be very gratified to learn
how many people are doing that now in private, truly independent research.
If Rife's research can be verified, there is no doubt that it will be due,
in part, to the efforts of John Crane.

A biography of Crane is being prepared for the internet, as well as
pertinent samples of his own writings to help illuminate the tortuous path
this technology has followed in last 46 years.

In the aforementioned book by John Crane, a very long bibliography was
compiled, apparently from John's own research as well as from Rife's
library. The following references were found:

* Rife, R.R., Rife Research Laboratory Manual 1920 to 1946: see
page 56, this book [A Study of Electron Therapy] for: History of
the Development of a Successful Treatment for Cancer, and Other
Virus, Bacteria and Fungi, Report No. Dev.-1042 Allied
Industries, 1953 pub. by Rife Virus Microscope Institute, San
Diego, Calif. Polarity Research Manual, Copyrighted '89 by John
F. Crane and Rife.
* Rife, R.R., The Rife Scrapbook, 1920 to 1971 containing some 400
publications about Rife and his world famous research.

In the copy I received of Crane's manual, page 56 was missing. In fact
several crucial pages are missing probably due to copying errors. And the
index indicated several segments which, also, were not there. The latter
deficiencies are almost certainly due to the disorganized method of
appending new data...it is basically a photocopy compilation. The final
Crane manual is the size of large city phone directory. All is as found,
except for some spelling corrections and notes, indicated in brackets to
obviate certain technical misunderstandings. I will append some
observations on the text in general in the near future, and any further
data that may be uncovered from Rife's original text. rsc, 27 September.
---------------------------------------------------------------------------

HISTORY OF THE DEVELOPMENT OF A SUCCESSFUL TREATMENT FOR CANCER AND OTHER
VIRUS, BACTERIA AND FUNGI

ROYAL RAYMOND RIFE

Introduction (TO CANCER)

Before my discovery of the cause of cancer and other diseases, I had sought
to find such evidence with standard Research microscopes. I observed all
types of malignant tissue to find some trace of the cause. I felt that the
start of malignancy would be originated by some type of micro-organism.

It became obvious that in order to find the cause, better means of
observation had to be developed. Thus five microscopes were designed and
built in the laboratory with a range of 5,000 to 50,000 X. Working in
magnifications of 17,000 X and higher revealed new cells and
micro-organisms requiring much skill and patience to focus and photograph.

After the isolation of the filtered virus and other pathogenic organisms,
the idea was conceived, that it would be possible to create an electronic
frequency that was in the correct coordination or resonance of the chemical
constituents of a given organism or virus, and to devitalize with said
frequency, the organism or virus in question.

The initial frequency instrument of this nature was first used and
developed in the laboratory in 1920. Due to the great advancement in the
field of electronics, these frequency instruments have steadily improved to
the present day.

The isolation of cancer virus and other micro-organisms was an
accomplishment with which I felt a great deal of pride. Finally in 1931, I
discovered the transformation of cancer virus and the successful treatment
for cancer and other diseases by actual observation of the universal
microscope while applying the frequency instrument. Thus, this data is
presented for evaluation. With the frequency instrument, no tissue is
destroyed, no pain is felt, no noise is audible, and no sensation is
noticed. A tube lights up and 3 minutes later the treatment is completed.
The virus or bacteria is destroyed and the body then recovers itself
naturally from the toxic effect of the virus and or bacteria. Several
disease forms may be treated simultaneously.

GENERAL DISCUSSION OF VIRUS OBSERVATION

The major portion of the cancer tests of the tumors used in the initial
tests were procured from the Paradise Valley Sanatarium in National City,
California. The pathology of these tumors was checked through their
laboratory as malignant.

The prime reason that viruses have never been observed in their true form
of their association with a disease is because the best standard research
microscopes will not show them; first, on account of the lack of great
enough magnification and second, owing to the minuteness of these
particles, it is impossible to stain them with any known method or
technique using acid or aniline dye stains; hence a substitute stain was
found. The viruses were stained with a frequency of light that coordinates
with the chemical constituents of the particle or micro-organism under
observation.

The variation of the light frequency is accomplished by use of a variable
monochromatic beam of light that is tuned to coordinate with the chemical
constituents of particle, virus, or micro-organism is observed by use of
the core beams from the patented Rife Microscope Lamps, which provide
illumination through a series of rotating quartz prisms in the universal
microscope and thence through the slide containing the specimens and on to
the eyepiece. Rotation of the light beams in the quartz prisms controls the
increase or decrease of the light frequency. With complete control of the
illuminating unit, a frequency is created that is in coordination with the
chemical constituents of the virus under observation and thus it is
possible to observe the virus in its chemical refractive index. The control
of the illumination (in the universal microscope and the other Rife
Research microscopes) is a most important factor in visualizing the virus
of any pathogenic micro-organism. This cannot be accomplished by any
conventional sources of illumination. This points out why other research
groups have failed to find cancer virus.

We believe and have proven to our satisfaction that the so-called virus is
in reality the premodal cell of a micro-organism. We also have proven that
it is the chemical constituents and chemical radicals of the virus under
observation which enacts upon the unbalanced cell metabolism of the body to
produce any disease that may occur. We have in many instances produced all
the symptoms of the disease chemically without the inoculation of any virus
or bacteria in the tissues of experimental animals.

We have classified the entire category of pathogenic bacteria into 10
individual groups. Any organism within its group can be readily changed to
any other organism within the ten groups depending upon the media withih it
is fed and grown. For example, with a pure culture of bacillus coli, by
altering the media as little as two parts per million by volume, we can
change that organism in 36 hours to a bacillus typhosis showing every known
laboratory test even to the Widal reaction. Further controlled alterations
of the media will end up with the virus of poliomyelitis or tuberculosis or
cancer as desired, and then, if you please, alter the media again and
change the micro-organism back to a bacillus coli.

METHODS OF CULTURE AND TECHNIQUES OF ISOLATION OF THE VIRUS OF CANCER

The methods and principles that were used in this procedure were as herein
related. An unulcerated breast mass that was checked for malignancy by
their laboratory and ourselves came to our laboratory from the Paradise
Valley Sanitarium of National Cirty, California. The experiments of 1931
and 1932 were conducted in our Point Loma Laboratory, then known as the
Rife Research Laboratory.

Ten millimeter blocks of this tumor (in 1932) were placed in "K" media and
incubated at 37.5 degrees C with no results. After many long procedures and
attempts to grow the cancer virus had failed, the discovery of the growth
method of cancer virus was found. A test tube containing a sample from the
unulcerated breast mass was sealed and placed in an argon gas filled loop
with 15 mm vacuum and activated with 5000 volts. This produced a decided
change of ionized cloudiness in the media. (This media was of tyrode
solution and desiccated slime (sic) intestine). This test tube was then
checked for cancer virus, but at this point none were visible. Then the
test tube was subjected to a 2-inch water vacuum and incubated for 24
hours. Upon examination the solution in the test tube was teeming with
cancer virus which were the most highly motile and the smallest in size of
any of the viruses previously isolated.

These BX or cancer viruses refracted a purplish red color with the
monochromatic beam.

We have not thoroughly determined the phenomena that takes place with this
technic of culturization, but we believe that this method brings the
organism from the ultraviolet band into the visibility of refraction. (This
method does not alter the virulence of the virus in any way). This virus is
bi-polar (and will attract to both the positive and negative poles), but
requiring both the + & - parts to produce a reaction in the tissues of the
experimental animals. Our method used in this procedure was as follows:

Albino rats were generally used. The animal chosen for this experimental
work is carried no less than 12 day through quarantine. The animal is
shaved at the point of inoculation and placed under a partial anesthesia.
The needle for inoculation is filled with triple sterilized petroleum jelly
and the inoculum and passed no less than 20 mm under the epidermis to the
point of inoculation. In 3 to 4 days almost invariably there is an open
lesion which appears in the thyroid area. This recedes at the end of that
time and the growth of the tumor starts at the seat of inoculation which is
a mammary gland. These tumors develop very rapidly owing to the metabolic
rate of the albino rat. In many cases these tumors have grown to weight
exceeding that of the animal. Upon surgical removal of this mass and upon
microscopical examination---a true malignancy is shown. That proved that
the virus was pathological. These experiments were carried through no less
than one hundred times with the same methods and careful technic with the
same end results. We sincerely believe that this leaves no doubt as to the
fact (that the BX organism initially isolated from the unulcerated human
tumor and recovered from the tumor produced by that BX virus and that BX
virus again recovered) that BX is the primary cause of cancer. We have in
our own classification called this virus of cancer--BX. We do not expect
any laboratory to be able to produce BX on account of the technic involved
and the lack of adequate optical equipment. This BX or any other virus
cannot be seen with the conventional microscope and illuminating systems as
we have explained often before. That these tiny live living entities (known
as BX virus) cannot be stained with any of the conventional acid or aniline
dye stains as they are much smaller in dimension than the molecular
particles of said stain and can be seen only by a frequency of light which
coordinates with their chemical constituents. All viruses require their own
individual frequency of the mono-chromatic beam to make them visible to the
human eye.

We have come to the conclusion that the illuminant in the fields of high
powered microscopy is a more important factor than the high power in
magnification of the microscope because without this source of illumination
these particles called virus are invisible with any amount of magnification
o we have used Koch's postulates in our methods of recovery which are that
the organism inoculated into the host must again be recovered in its true
form from the host and thus, as stated before this has been repeated
hundreds of times proving to our own satisfaction that BX or cancer virus
is the cause of malignancy.

This BX virus can be readily changed into different forms of its life cycle
by the media upon which it is grown.

A pure culture of cancer virus is taken from a known tumor and filtered
through a 000 Berkefeld (sic) W porcelain filter under 10 mm vacuum. From
this filtrate a sample is drawn off with a thin glass tube which has
previously been heated, sterilized, and drawn to a fine orifice. One
micro-drop is placed on a quartz slide and covered with a quartz cover
slip. The slide is positioned on the stage of the universal microscope. The
universal microscope is focused on the cancer virus and a 16 mm or 35 mm
camera is mounted to expose the (positive) negatives. The (positive)
negatives are developed and dried and then placed in a 1000 watt enlarger
and exposed for .9 second to a 3 inch by 4 inch glass slide negative which
is developed in microdal fine grain developer. From this slide, the
photomicrograph copies are reproduced.

CHEMICAL RELATIVITY TO CARCINOMA Coordinative Constituents

(A) Dibenzanthracene as a carcinogenetic agent.

1. Di-derivative of dis[sic, cis?]
meaning separated
by or doubling up.

2. Benz - (Benzene C6 H6)
Benzol as a C6 H6
derivative C6 H6 nCH2

3. Anthracene - C14 H10 =
3C6 H6 - C4 H8 white
solid Hydrocarbon used in preparation
of indigo and aliza[rin].

(B) Napthalene (C10 H8) almost
the same as C14 H10 (moth balls)

Cancer Virus Characteristics

1. Not destroyed by X-Ray, ultra violet or infrared ray.
2. Thermal death point in 24 hours is 42 deg. C or 107.6 deg. F.
3. Sporogenous.
4. Non liquefying (media).
5. Non chromogenic and non aerobic.
6. - (Cathode) polarization.
7. Width of ovoid or microorganism is 1/20 micrometer.
8. Length of ovoid micro-organism is 1/15 micrometer.
9. Flagellated and nonparasitic.
10. Highly motile and plastic.
11. Highly pathogenic.
12. Seen at 12 3/16 degrees angle of refraction on universal microscope.
13. Color of chemical refraction: purple red, which results from the
coordinative constituents reaction upon the degree of light frequency
applied.

TECHNIQUE OF "BX" INOCULATION

Our method of inoculation of experimental animals with "BX", the virus of
cancer, is as follows:

The animal is first shaved and sterilized with alcohol and iodine solution
at the point of inoculation and placed under partial anesthesia. This
avoids subjecting the animal to shock. An extra long, very small needle is
used. The needle is filled with the inoculum and the needle placed in the
syringe. The needle is inserted no less than 30 mm from the point of
inoculation to the epidermis. The point of inoculation is in most cases by
a mammary gland for the reason that the "BX" involved was recovered from an
unulcerated human breast mass.

In 3 to 4 days a lesion appears in the thyroid area. The cause of this is
unknown, but the lesion recedes and heals over and a growth starts in the
mammary gland of the experimental animal. These growths have exceeded the
weight of the experimental animal in many cases. The tumor is surgically
removed and the "BX" is again recovered in all cases.

An important factor and check is to make at least 10 transplants from the
initial isolation of "BX". These transplants are made at 24 hour intervals
in the original "K" media. It increases the virulence and speeds up the
growth of the tumor. With these experiments that have been repeated on over
100 experimental animals, we are convinced that this method definitely
proves the virulence and pathology of "BX" virus.

If there are any workers interested in following this technic, we will
furnish them with the formula of "K" media and all of the basic principles
involved. However, it is beyond the scope of the average microscope to
visualize these minute virus.

THE TREATMENT OF "BX" OR CANCER

The actual cure of cancer in experimental animals occurs with the use of
our frequency instrument. To attain these astounding results, a long and
tedious process is started to determine the precise setting of the
frequency instrument that is the mortal oscillatory rate of this virus.
When the setting is found, it is repeated 10 consecutive times after the
frequency instrument has been placed back to the same setting before a
specific frequency is recorded. These results are observed under the high
power of the universal microscope and when the mortal oscillatory rate is
reached, the "BX" forms appear to "blow up" or disintegrate in the field.
The inoculated animals are then subjected to the same frequency to
determine if the effect is the same on the "BX" virus in the tissues of the
experimental animals as with the pure culture slides; these successful
tests were conducted over 400 times with experimental animals before any
attempt was made to use this frequency on human cases. (breaks here with a
period. The next page comes after several pages describing viral
characteristics as compiled by Crane from Rife notes and other information)

...of carcinoma.

The first clinical work on cancer was completed under the supervision of
Dr. Milbank Johnson, M.D. which was set up under the special medical
Research Committee of the University of Southern California. Sixteen cases
were treated at the clinic for many types of malignancy. After 3 months, 14
of these so-called hopeless cases were signed off as clinically cured by
the staff of five medical doctors and Dr. Alvin G. Foord, M.D., Pathologist
for the group. The treatment consisted of 3 minutes duration using the
frequency instrument which was set on the mortal oscillatory rate for "BX"
or cancer (at 3 day intervals). It was found that the elapsed time between
treatments attains better results than cases treated daily. This gives the
lymphatic system an opportunity to absorb and cast off a toxic condition
which is produced by the devitalized dead particles of the "BX" or cancer
virus. No rise of body temperature was perceptible in any of these cases
above normal during or after the frequency instrument treatment. No special
diets were used in any of this clinical work, but we sincerely believe that
a proper diet compiled for the individual would be of benefit.

THE DETERMINATION AND DIAGNOSIS OF CANCER

We can determine in over 90% of the cases of persons having carcinoma by
the examination of a blood smear (with the technic heretofore explained) in
30 minutes. We have also found that in many types of epithelioma that the
carcinoma tissue carries no conductivity with a pendulum galvanometer which
enables us to outline and determine the location of a tumor without the use
of X-Ray photographs. It has also been determined that any case of
malignancy treated with either X-Ray or radium or other radio-active
materials shows decided radio-activity and harmful tissue effects for many
months after the treatments have been given. Destroyed tissue or tissue
that has been harmed is a natural parasitic feast. We have also found that
tumors treated with this method respond less readily to the treatment of
our frequency instruments.

RESEARCH ON BACILLUS X (CANCER VIRUS) AND METHODS AND TECHNIC OF ISOLATION

In 1920 to 1925, some 20,000 pathological tissues were sectioned and
stained in the most precise and careful manner, but failed to show any
unknown bacteria or foreign material under the highest power of our No. 1
microscope. Attempts were made to culture blocks of tissue taken in the
most sterile manner from an unulcerated breast mass of proven (BX)
malignancy. These blocks were cut in 5 mm cubes and placed in test tubes
containing "K" media. This media is made from dehydrated, desiccated pig
intestine and a tyrode solution. "K" media has the faculty of transforming
most organisms into their transitional state and is used with
micro-organisms to liberate their virus or premodal cells.) The tubes were
incubated at various temperatures from 30 to 40 degrees with no results.
Then one of the experiments showed results. The test tubes were placed in
an Argon gas filled loop excited by 5,000 volts and again examined after 24
hours. There was a decided change and a cloudiness in the culture media,
however microscopic examination showed no organisms were visible. By
chemically analyzing the "K" media, it was concluded that the electronic
bombardment had produced an ionization in the "K" media. To counteract this
ionization, the test tubes were placed in a 2-inch water vacuum and
incubated at 37.5 degrees C for 24 hours. Subsequent examination at 20,000
X revealed the "K" media to be teaming with the smallest of any forms
observed. These forms of the cancer virus were called "BX" and refract a
purplish red in a monochromatic beam of the microscope.

This method of ionization and oxidation brought the chemical refraction of
the "BX" out of the ultra-violet and into the visible band of the spectrum.
Owingh to the fact that these test tube specimens had gone through so many
trials, we again started from scratch and repeated this method 104
consecutive times with identical results. The "BX" virus was given a
complete breakdown to determine its chemical constituents and
characteristics, which are previously noted in this report.

By continued microscopical study and stop motion photography, it was found
that the "BX" virus had many changes and cycles as so with other
micro-organisms. The virus can be readily changed to other forms or cycles
of themselves by the media upon which they are grown. By altering the "K"
media slightly acid, we no longer have a "BX" as we have classified this
cancer virus, but we have what we term a "BY". In this stage or form, it is
still a virus, but considerably enlarged from the initial "BX". Still
retaining a purple red refractive index, but will no longer pass the
porosity of the W (?) porcelain or diatomaceous earth filter. In this
stage, the "BY" requires a much coarser "N" filter.

The next stage finds this micro-organism, now known as the monococcoid form
in the monocytes of the blood of over 90% of carcinomatous individuals.
This form can be readily seen when properly stained with a combination of a
silver nitrate and gentian violet with the standard research microscope.

As we change the media again and this time going from a fluid to a hard
base media (using asparagus or tomato agar), we no longer have a "BX", or
" BY", or monococcoid micro-organism, but we have a cryptomyces pleomorphia
fungi. Any of these forms can be changed back to "BX" within a period of 36
hours and will produce in the experimental animal a typical tumor with all
the pathology of true neoplastic tissue, from which we can again recover
the "BX" micro-organism. This complete process has been duplicated over 300
times with identical and positive results.

After one year, we take this same stock culture of dormant cryptomyces
pleomorphia fungi and plant it back on its own asparagus base media; there
is no longer a cryptomyces pleomorphia, no longer a monococcoid organism
such as is found in the monocytes of the blood, there is no longer a "BX"
or "BY" form, but there is, from the initial virus isolated directly from
an unulcerated human breast mass, a BACILLUS COLI, that will pass any known
laboratory methods of analysis.

We are positive from our careful work and technic, that the causative agent
of malignancy can be definitely identified as bacillus coli as the basic
form.

"BX" is a bipolar virus, that is, retraction occurs to both positive and
negative poles, but both the positive and negative forms of this virus are
required to produce tumors in experimental animals. We have never publicly
announced that "BX" is the cause of cancer, but we have succeeded in
producing from its inoculation the tumors as stated before with all the
true characteristics and pathology of neoplastic tissue from which we have
repeatedly recovered the "BX" virus. Many researchers have attempted to
repeat this technic but have failed for the prime reason of the lack of an
adequate microscope.

THE LIFE CYCLE AND TREATMENT OF TUBERCULOSIS

The purpose of this paper is to describe some of the principles and methods
of the isolation and culturization of the Bacillus of Tuberculosis and its
treatment. This particular organism is one of the more complicated of the
pathogens and its process of development. We classify this organism in the
Fungoid Group although it is not considered in the same field of mycology
as it has no spores or skis-spores. This organism was isolated in pure
culture in 1879 by Robert Koch and remains to this day a masterpiece of
patient work. He succeeded in isolating the bacillus of tuberculosis in the
pure form by devising a method of plating technic. He was the first to
contrive and pour the agar petri dish plates. By this method of isolating
the colonies, as they would appear on the surface of the plates, he was
able in due time to continually produce a pure strain of the organisms.
These organisms in the pure state pass from the initial rod form through
nine stages in the fungoid group. Most all observers have seen the more
common forms in the branching and mycelium stages. These forms were
recorded and photographs same were made by the writer and Dr. A.I. Kendall,
M.D. in Dr. Kendall's laboratory in Northwestern University in 1932 and
from these initial forms, we succeeded in isolating by the alteration of
the media, the other eight branching forms. Before succeeding in the
attainment of the virus form, we considered this virus form as the premodal
cell of the bacillus of Tuberculosis. For example: If the initial rod form
of the organism is inoculated into the experimental animal, the lymphatic
chain produces in from 10 to 12 weeks all the symptoms of the disease and
by inoculating the virus or premodal cell form, the same symptoms are
noticed in 36 to 48 hours. This was repeated many times by the writer in
1932 with 100% identical results. Tests point out that this occurs not only
with the bacillus of Tuberculosis, but in many cases with other organisms;
in this form, they also produce the disease. The Universal microscope shows
that virus, under refractive light to be a jade green in color, highly
refractive, and non-motile. We find with this organism, the same as with
all pathogenic organisms, that if the parent rod is motile, the virus of
that parent rod is motile. If non-motile, both are non-motile. there is no
other form of these fungoid growths through the complete life cycle that
was found to produce the disease. So we have often stated, the so-called
incubation period of a micro-organism is in reality a cycle of reversion.
Until that organism grows to a transitional or premodal state, it does not
produce the disease. We have found that this virus of the bacillus of
tuberculosis is the so-called poison molecule of Voghn. In experimental
work with anti-toxins and vaccines, Vaghn found, as did Robert Koch, that
they could definitely destroy the rod form of the organism, but the
experimental animals would invariably die. We feel that the phenomena that
they created with their anti-toxins and vaccines was merely releasing from
the rod form, the virus, which in this form re-enacts upon the dead body of
the rod and produces toxemia and death to the patient. With our Frequency
Instrument treatment for this disease in question, the devitalizing
frequencies of the rod form and virus form are used simultaneously and the
results attained have been successful on experimental animals and on human
individuals. There is much that can be accomplished by the continuances of
this research and experimental work on one of the most complicated of the
pathogenic micro-organisms.

Rife pro Rife machine

"Royal rife developed "Five" Rife machine prototypes ,the fith rife machine(beam ray)was reported to be the most powerful"

""I can assure you that no one, not even myself, could help but be astounded at the results we are now obtaining with the assistance of our new machines and our new band of MOR's.(Mortal oscillatory rate)" (Letter from Dr. Johnson to Dr. Gruner (copy sent to Dr. Rife) dated, November 4, 1936."."

"None of Dr. Rife's previous instruments ever had the capability that this instrument had.. Dr. Johnson pointed this fact out in his letter. "The major difference between this new Rife Ray #5 Clinical instrument and Dr. Rifeâ€™s previous instruments is the fact that this new instrument could produce over one hundred harmonic side bands simultaneously. It was this new harmonic sideband capability in this Beam Ray Clinical instrument which makes this sweep we are discussing on this page possible."

The worlds most advanved multi purpose Fully Automatic Rife/Hoyland System Read more here