A
DISCUSSION OF LABORATORY RESEARCH
Royal
R. Rife
June
14, 1958
We
have proven definitely that cancer is a virus or the filterable
form and pathogenic portion of chemical constituents that
produces the disease. In 3 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
with 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 causative 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 will 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.
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 media made of a tyrode solution,
which 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 thru 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 polarized light. We cannot use polarized light because it
takes in everything. The light frequency is segregated into the
desired monochromatic 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 predominate chemical factor and its radicals.
We work only on the predominate 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 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.
I
stated years and years ago, that when the causative agent of
malignancy would be found, it would be found by a
micro-organism. Not unlikely, a 80 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
only other cells which have no figioytosis 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 longer have a B-X
or a B-Y; but we have a cryptomyses pleomorphia fungi, with all
its 14 stages; clear from the original hyphae from the spores
and the ascospores, on down the line. Any one of these 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 crytomyces 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 hove a crytomyces
pleomorphia fungi, or a B-X, or a B-Y, or a
rnono-coçcoi.d micro-organism, we have with every known
laboratory test - a B. coli ( from an organism of virus that was
filters 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-toxins 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 use 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.
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