June 14, 1958

We have proven definitely that cancer is a virus or the filterable form and
pathogenic portion of chemical constituents that produce the disease. In 8
out of 10 cases we can produce the disease or the symptoms of the disease
without any bacteria. I have a large slide file containing approximately
20,000 cancer tissue slides. They do not amount to much as far as the virus
of cancer is concerned. They show something, but they did not show the
virus of cancer to me. Later I found the virus after designing and building
five highly specialized virus microscopes.

I produced cancer tumors in rats from a virus which I isolated by
filtration from an unulcerated human breast mass, transplanting the virus
through a process of ionization and oxidation in a Tyrode solution rich
with "K" media that Dr. A.I. Kendall developed at Northwestern University.
I can take any bacteria relative to cancer and plant it in this medium.
After 24 to 36 hours, the bacteria will be in the transitional state. In
this state the virus is shed as the primordial cell from the bacteria. The
virus will produce cancer.

It is an impossibility to stain these filterable forms. Over a period of
many years I have developed an excellent technique wirth all types of
stains, but I've found none that will stain the virus.

When I first started work on this research in 1921, it was my presumption
that when the causitive agent of malignancy would be found, it would be
found to be caused by a micro-organism. Not unlikely, a so-called
non-pathogenic micro-organism which we have with us at all times. The
etiology of this theoretical and applied biology can no longer be denied
and I have demonstrated it time and again.

(page 2)

The shift in the metabolism of an individual may also alter that
micro-organism into something else. That I proved definitely years later.

I developed the first microscope for the work of studying these tissues.
With my best methods and techniques of staining I found nothing. Then by
using the "K" media made of a tyrode solution, which is a basic 9 elements
of salt and pig-gut, desiccated and dehydrated; this media has a faculty of
transforming micro-organisms into what we term the transitional state. In
that particular state after 36 hours, we found granular particles that are
a virus from this organism, free swimming in the state. We also found them
in the ends of the rod forms, so that they will refract to a proper color
of index of light refraction. We know that we can transplant this culture
and we can produce the symptoms of cancer. But we do not see the virus.

We come back into the field of optics again. Now as we take our intense
beam of light and pass it through the condenser system of our microscope we
produce a frequency of light that is in coordination with the chemical
constituent of the virus under observation.

In our microscope we use two rotating wedge shaped quartz prisms. As that
intense needle point beam of light is passed through the condenser lenses
and up into the optical system of the microscope, we rotate the prisms at
different degrees of refraction. In this way we produce a frequency of
light that is in coordination with the chemical constituents of the virus
under observation. This is the same as polarized light, but it is not (page
3) polarized light. We cannot use polarized light because it takes in
everything. The light frequency is segregated into the desired
mono-chromatic beam of light by varying the rotating quartz prisms. In this
way we find the proper index of refraction of light. We bend the light rays
through the circular angles until the proper frequency of light is found
that will show the virus in their own true characteristic chemical colors.
Then we find the predominant chemical factor and its radicals. We work only
on the predominant of course because that is the one that we see. As an
example the filterable form of the B. typhosus is placed on a slide and
focused in under the microscope. The prisms are set for the proper degree
of refraction for light for the coordinative chemical constituents and the
virus is brought into view and final focus. The virus of B. typhosus has
gone through a triple filtration of "W" Berkefeld filters and the liquid is
just as clear as a drop of dew. We see there beautiful turquoise blue
bodies swimming through the field. Brilliant!! Now if the prisms are turned
1/10th of one degree in rotation, there will be a perfectly blank field. If
the filterable form of B.Coli is placed on the slide, which belongs to the
same group as B.typhosus, and focused in with the microscope and rotating
prisms, the virus will be a reddish brown color. When this procedure is
repeated with the virus of cancer, we see a purplish red primordial cell
that is highly motile.

Now if the bacteria that we are isolating is motile, then the virus that is
shed from the bacteria is always motile. For example: if you take the virus
from tuberculosis, it is non-motile. The bacteria of tuberculosis is a
non-motile micro-organism.

(page 4)

I stated years and years ago, that when the causitive agent of malignancy
would be found, it would be found [to be] a micro-organism. Not unlikely, a
so-called non-pathogenic organism. In one stage not unlikely a blood
disease. That I have proven.

We have taken B-X or cancer virus that was isolated directly from an
unulcerated breast mass, injected it into the animal, and recovered the
virus back again. We have completed this over four hundred times
consecutively with the same technique to prove this method. After 100
consecutive times, it can be placed on the records.

Now we alter the media. We no longer have what we call a B-X; we have a
B-Y. This will no longer pass the "W" Berkefeld filter. We use a much
coarser porosity known as the "N". If we alter the media again, we see a
monococcoid micro-organism. This micro-organism can be seen with a good
research microscope, with the proper staining method. We stain this
micro-organism. We find it only in the monocytes of the blood. The
monocytes are the only other cells which have no figicytosis. When we alter
the media once again, we come from a fluid media into a hard base media. We
use either asparagus, or tomato with our agar. Asparagus is better, but
tomato will work. We no longer have a B-X or B-Y; but we have a cryptomyces
pleomorphia fungi, with all its 14 stages; clear from the original hyphae
from the spores and the ascospores, on down the line. Any one can be thrown
back in 24 hours into a B-X by putting them back on "K" medium, to be
capable of producing the disease. If we allow the cryptomyces pleomorphia
fungi to stand as a dormant stock culture for one year and plant it back in
its own original asparagus base medium, we no longer have a cryptomyces
pleomorphia fungi, or a B-X, or a B-Y, or a mono-coccoid micro-organism, we
have with every known laboratory test - a B. coli (from an organism of
virus that was filtered and isolated from an unulcerated breast mass of a
woman.)

I worked a great deal on tuberculosis. I isolated a virus from tuberculosis
which I consider is similar to what has been heretofore known as the poison
molecule of Vaughn that Vaughn of Ann Arbor isolated many years ago. He did
not isolate the organism but he isolated a chemical particle. Koch (Robert
Koch of Germany) originally isolated the virus of tuberculosis. He produced
the vaccines and anti-toxines that would kill the bacilli of tuberculosis,
but they would also kill the patient. Simply because with any known method
or means that you release from tuberculosis, this virus or the so-called
" poison molecule of Vaughn" they react upon the dead bodies of the rod form
and produce toxemia and death. I finally found an electronic frequency that
would kill these bacteria. I found the M.O.R. of the virus of Tuberculosis
and also the M.O.R. frequency for the rod form which we have had for years.
If two of the frequencies are used simultaneously, or one right after the
other, over the same carrier wave, the patient gets well, and the guinea
pig gets well. If you use either frequency individually you either kill the
patient or animal, or you accomplish nothing.

END

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