Rife] Rife Research Documentation

[Guest guest]

" Michael Tigchelaar " <michaeltigchelaar

Tue, 29 Aug 2006 18:30:55 -0700 (PDT)

[Rife] Rife Research Documentation

 

 

 

 

HISTORY OF THE DEVELOPMENT OF A SUCCESSFUL TREATMENT FOR CANCER AND

OTHER VIRUS, BACTERIA AND FUNGI by 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.

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. Ford, 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 technique 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.

 

 

 

 

------------ --------- --------- ---