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 within 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.
THE PROCESS TO PRODUCE THE CANCER VIRUS PHOTOMICROGRAPH
(Copyright 1953)
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
-
Not destroyed by X-Ray, ultra violet or infrared ray.
-
Thermal death point in 24 hours is 42 deg. C or 107.6 deg. F.
-
Sporogenous.
-
Non liquefying (media).
-
Non chromogenic and non aerobic.
-
- (Cathode) polarization.
-
Width of ovoid or microorganism is 1/20 micrometer.
-
Length of ovoid micro-organism is 1/15 micrometer.
-
Flagellated and nonparasitic.
-
Highly motile and plastic.
-
Highly pathogenic.
-
Seen at 12 3/16 degrees angle of refraction on universal microscope.
-
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 technique. 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.