Royal Raymond Rife
1888-1971
Royal Raymond Rife was trained for six years by the Carl
Zeiss Optical Company in Germany. He became the inventor of powerful
microscopes, leading to the discovery of a beneficial phenomenon dealing with
viruses. Rife received the backing of Mr. Timken, of the Timken Roller Bearing
Company, who supplied funds to establish a laboratory in San Diego to finance
his research. Rife reasoned that if he was going to find a cure for diseases
such as cancer, it was important to be able to see the live virus that caused
the disease. In 1920, Royal Rife designed the first of several highly advanced
microscopes, recognized as the most powerful in the world, and the only one
that could be used to see viruses alive.
Rife’s microscopes had resolutions and
magnifications far more powerful than others of his day (or even today). Rife”s
Universal Microscope (1933) magnified 31,000 times; other microscopes of his
day magnified only 3,000 times. Rife found that making a microscope with
extreme magnification was not sufficient to see a colorless virus. Staining
them with existing aniline dyes was unsuccessful because the virus was too
small to absorb the colloidal particles. Rife noted that the different
frequencies of light caused certain microorganisms to illuminate (light up) in
their own resonant colors. So he invented a system of rotating prisms to select
the appropriate light frequency (color), essentially staining the specimen with
light.
Rife’s Microscope, the largest model
of which consisted of 5,682 parts and required a large bench to accommodate it,
overcame the greatest disadvantage of the electron microscope and its inability
to reveal specimens in their natural living state. With his invention, Rife was
able to look at living organisms. What he saw convinced him that germs could
not be the cause, but the result, of disease; that, depending on its state, the
body could convert a harmless bacterium into a lethal pathogen, that such
pathogens could be instantly killed, each by a specific frequency of light; and
that cells, regarded as the irreducible building blocks of living matter, are
actually composed of smaller cells, themselves made up of even smaller cells,
this process continuing with higher and higher magnification in a sixteen—step,
stage—by—stage journey into the micro—beyond.
Extrapolating from this resonant
effect of light, Rife experimented with electromagnetic radio waves and
discovered that for each type of virus, there was a particular resonant
frequency that would cause it to burst into pieces and be destroyed. Every substance
in the world has its own unique vibration, and this is true for human cells,
tissues, and organs as well. The same is
true for pathogens and diseases as they are also associated with specific
frequencies. He subjected test animals
in his laboratory to lethal doses of pathogenic germs and found that he could
invariably save their lives by subjecting their bodies for a few minutes to the
electrical energy of the properly chosen frequency.
Therefore, before the year 1930, he
had built his first microscope and demonstrated that he could electronically
kill pathogenic microorganisms. In the 1930’s in the United States, Royal
Raymond Rife used this insight to create a special optical microscope with
quartz lenses and rotating quartz prisms, polarized (monochrome) light, 5682
parts, and a much higher magnification of 60 thousand times and a resolution of
31 thousand times than was usual for optical microscopes.
The Science Museum (South Kensington,
London SW7 2DD, UK) possesses a Royal Rife Microscope. It has the inventory
number 1990-667 and was presented to the Science Museum in 1990 by the London
School of Hygiene and Tropical Medicine. The School had been given the Scope by
the daughter of the late owner, Dr B W Gonin, some fourteen years previously. This
is one of the very last Rife Microscopes in existence.
Dr. Royal Raymond Rife Created the
Original ‘Royal Rife Machine’, a frequency generating device which was used to
cure terminally ill cancer patients through selective electronic frequency
treatment programs. From the 1950s to 2010 A number of research scientists,
working independently, have slowly been verifying the scientific principles
upon which Rife”s clinical cures of the 1930s were based. A body of recognized
scientific evidence now overwhelmingly supports the original cancer theories
articulated and demonstrated by Rife 80 years ago. This includes modern AIDS
researchers.
In
the 1950s, John Crane-engineer, machinist, laboratory analyst, health
researcher and inventor-became Rife”s partner. Crane, born in 1915, worked at
Rife”s side from 1950 until Rife”s death in 1971. During this time, he learned
all the secrets of Rife”s cancer treatment . . . and all the details of its
suppression. Together, the two men designed and constructed new and better
equipment, and managed to interest a new generation of doctors in the
possibilities of a genuine, lasting and painless cancer treatment. And again
the authorities struck. Crane was jailed, equipment was smashed, records were
destroyed. Again the motives driving on the forces of suppression were the
same. By sharing the long hidden facts, as well as thousands of documents
preserved from the 1930s, Crane has enabled the full story to be told.
A Rife type microscope system where a matched
pair of objective and eyepiece lens systems are being used in conjunction with
a single machined block of quartz or clear sapphire (hidden from view by
partition). Determine a machined shape of all surfaces, relative
orientation, and dimensions of the machined block to obtain 500,000 power
magnification, with 5 angstrom resolution. Be sure to precisely
define the surface of both the entrance and exit ports for the light going from
the objective into the block and going to the eyepiece.
Assume focal length of objective lens is .2 meters with a
convergence angle of 2 degrees and the objective lens is 250 power. HINT:
Use whatever wavelength of light you want that is compatible with optical
materials used throughout the optical system. You will use total internal
reflection inside the machined block to cut down on (stop) light intensity loss
and you are allowed to use one normal mirror surface (i.e. silver deposited on
machined/polished plane surface).
THE SMITHSONIAN REPORT
The Universal Microscope
It is only a reasonable supposition, but already, in
one instance, a very successful and highly commendable achievement on the part
of Dr. Royal Raymond Rife of San Diego, California, who, for many years, has
built and worked with light microscopes which far surpass the theoretical
limitations of the ordinary variety of instrument, all the Rife scopes
possessing superior ability to attain high magnification with accompanying high
resolution.
The largest and most powerful of these, the Universal Microscope, developed in
1933, consists of 5,682 parts and is so called because of its adaptability in
all fields of microscopical work, being fully equipped with separate substage
condenser units for transmitted and monochromatic beam dark-field, polarized,
and slit-ultra illumination, including also a special device for
crystallography. The entire optical system of lenses and prisms as well as the
illuminating units are made of block-crystal quartz, quartz being especially
transparent to ultraviolet radiations.
This illuminating unit used for examining the filterable forms of disease
organisms contains 14 lenses and prisms, 3 of which are in the high-intensity
incandescent lamp, 4 in the Risley prism, and 7 in the achromatic condenser
which, incidentally, has a numerical aperture of 1.40. Between the source of
light and the specimen are subtended two circular, wedge-shaped, block-crystal
quartz prisms for the purpose of polarizing the light passing through the
specimen, polarization being the practical application of the theory that light
waves vibrate in all planes perpendicular to the direction in which they are
propagated.
Therefore, when light comes into contact with a polarizing prism, it is divided
or split into two beams, one of which is refracted to such an extent that it is
reflected to the side of the prism without, of course, passing through the
prism while the second ray, bent considerably less, is thus enabled to pass
through the prism to illuminate the specimen.
When the quartz prisms on the universal microscope, which may be rotated with
vernier control through 360 degrees, are rotated in opposite directions, they
serve to bend the transmitted beams of light at variable angles of incidence
while, at the same time, a spectrum is projected up into the axis of the
microscope, or rather a small portion of the spectrum to the other, going all
the way from the infrared to the ultraviolet.
Now, when that portion of the spectrum is reached in which both the organism
and the color band vibrate in exact accord, one with the other, a definite
characteristic spectrum is emitted by the organism.
In the case of the filter-passing form of the Bacillus Typhosus, for instance,
a blue spectrum is emitted and the plane of polarization deviated plus (+) 4.8
degrees.
The predominating chemical constituents of the organism are next ascertained
after which the quartz prisms are adjusted or set, by means of vernier control,
to minus (-) 4.8 degrees (again in the case of the filter-passing form of the
Bacillus Typhosus) so that the opposite angle of refraction may be obtained.
A monochromatic beam of light, corresponding exactly to the frequency of the
organism (for Dr. Rife has found that each disease organism responds to and has
a definite wave length, a fact confirmed by British medical research workers)
is then sent up through the specimen and the direct transmitted light, thus
enabling the observer to view the organism stained in its true chemical color
and revealing its own individual structure in a field which is brilliant with
light.
The objectives used on the universal microscope are a 1.12 dry lens, a 1.16
water immersion, a 1.18 oil immersion, and a 1.25 oil immersion. The rays of
light refracted by the specimen enter the objective and are then carried up the
tube in parallel rays through 21 light bends to the ocular, a tolerance of less
than one wave length of visible light only being permitted in the core beam, or
chief ray, of illumination.
Now, instead of the light rays starting up the tube in a parallel fashion,
tending to converge as they rise higher and finally crossing each other,
arriving at the ocular separated by considerable distance as would be the case
with an ordinary microscope, in the universal tube the rays also start their
rise parallel to each other but, just as they are about to pull them out
parallel again, another prism being inserted each time the rays are about ready
to cross.
These prisms, inserted in the tube, which are adjusted and held in alignment by
micrometer screws of 100 threads to the inch in special tracks made of
magnelium (magnelium having the closest coefficient of expansion of any metal
to quartz), are separated by a distance of only 30 millimeters.
Thus, the greatest distance that the image in the universal microscope is
projected through any one media, either quartz or air, is 30 millimeters
instead of the 160, 180, or 190 millimeters as in the empty or air-filled tubes
of an ordinary microscope, the total distance which the light rays travel
zigzag fashion through the universal tube being 449 millimeters, although the
physical length of the tube itself is 229 millimeters.
It will be recalled that if one pierces a black strip of paper or cardboard
with the point of a needle and then brings the card up close to the eye so that
the hole is in the optic axis, a small brilliantly lighted object will appear
larger and clearer, revealing more fine detail, than if it were viewed from the
same distance without the assistance of the card.
This is explained by the fact that the beam of light passing through the card
is very narrow, the rays entering the eye, therefore, being practically
parallel, whereas without the card the beam of light is much wider and the
diffusion circles much larger. It is this principle of parallel rays in the
universal microscope and the resultant shortening of projection distance
between any two blocks or prisms plus the fact that objectives can thus be
substituted for oculars, these "oculars" being three matched pairs of
10 millimeter, 7 millimeter, and 4 millimeter objectives in short mounts, which
would make possible not only the unusually high magnification and resolution
but which serve to eliminate all distortion as well as all chromatic and
spherical aberration.
Quartz slides with especially thin quartz cover glasses are used when a tissue
section or culture slant is examined, the tissue section itself also being very
thin. An additional observational tube and ocular which yield a magnification
of 1,800 diameters are provided so that that portion of the specimen which is
desired to be examined may be located so that the observer can adjust himself
more readily when viewing a section at a high magnification.
The universal stage is a double rotating stage graduated through 360 degrees in
quarter-minute arc divisions, the upper segment carrying the mechanical stage
having a movement of 40 degrees, plus or minus. Heavily constructed joints and
screw adjustments maintain rigidity of the microscope which weighs 200 pounds
and stands 24 inches high, the bases of the scope being nickel cast-steel
plates, accurately surfaced, and equipped with three leveling screws and two
spirit levels set at angles of 90 degrees. The coarse adjustment, a block
thread screw with 40 threads to the inch, slides in a 1 1/2 dovetail which
gibes directly onto the pillar post. The weight of the quadruple nosepiece and
the objective system is taken care of by the intermediate adjustment at the top
of the body tube. The stage, in conjunction with a hydraulic lift, acts as a
lever in operating the fine adjustment. A 6-gauge screw having 100 threads to
the inch is worked through a gland into a hollow, glycerine-filled post, the
glycerine being displaced and replaced at will as the screw is turned clockwise
or anticlockwise, allowing a 5-to-1 ratio on the lead screw. This, accordingly,
assures complete absence of drag and inertia. The fine adjustment being 700
times more sensitive then that of ordinary microscopes, the length of time
required to focus the universal ranges up to 1 1/2 hours which, while on first
consideration, may seem a disadvantage, is after all but a slight inconvenience
when compared with the many years of research and the hundreds of thousands of
dollars spent and being spent in an effort to isolate and to look upon
disease-causing organisms in their true form.
Working together back in 1931 and using one of the smaller Rife microscope
having a magnification and resolution of 17,000 diameters, Dr. Rife and Dr.
Arthur Isaac Kendall, of the department of bacteriology of Northwestern
University Medical School, were able to observe and demonstrate the presence of
the filter-passing forms of Bacillus Typhosus. An agar slant culture of the
Rawlings strain of Bacillus Typhosus was first prepared by Dr. Kendall and
inoculated into 6 cc of "Kendall" K Medium, a medium rich in protein
but poor in peptone and consisting of 100 mg. of dried hog intestine and 6 cc
of tyrode solution (containing neither glucose nor glycerine) which mixture is
shaken well so as to moisten the dried intestine powder and then sterilized in
the autoclave, 15 pounds for 15 minutes, alterations of the medium being
frequently necessary depending upon the requirements for different organisms.
Now, after a period of 18 hours in this K Medium, the culture was passed
through a Berkefeld "N" filter, a drop of the filtrate being added to
another 6 cc. of K Medium and incubated at 37 degrees C. Forty-eight hours
later this same process was repeated, the "N" filter again being used,
after which it was noted that the culture no longer responded to peptone
medium, growing now only in the protein medium. When again, within 24 hours,
the culture was passed through a filter-the finest Berkefeld "W"
filter, a drop of the filtrate was once more added to 6 cc.of K Medium and
incubated at 37 degrees c., a period of 3 days elapsing before a new culture
was transferred to K Medium and yet another 3 days before a new culture was
prepared. Then, viewed under an ordinary microscope, these cultures were
observed to be turbid and to reveal no bacilli whatsoever. When viewed by means
of dark-field illumination and oil-immersion lens, however, the presence of
small, actively motile granules was established, although nothing at all of
their individual structure could be ascertained. Another period of 4 days was
allowed to elapse before these cultures were transferred to K Medium and
incubated at 37 degrees C for 24 hours when they were then examined under the
Rife microscope where, as was mentioned earlier, the filterable typhoid
bacilli, emitting a blue spectrum, caused the plane of polarization to be
deviated plus 4.8 degrees. Then when the opposite angle of refraction was
obtained by means of adjusting the polarizing prisms to minus 4.8 degrees and the
cultures illuminated by a monochromatic beam coordinated in frequency with the
chemical constituents of the typhoid bacillus, small oval actively motile,
bright turquoise-blue bodies were observed at a magnificatinn of 5,000
diameters, in high contrast to the colorless and motionless debris of the
medium. These observations were repeated eight times, the complete absence of
these bodies in uninoculated control K Media also being noted.
To further confirm
their findings, Drs. Rife and Kendall next examined 18-hour-old cultures which
had been inoculated into K Medium and incubated at 37 degrees C., since it is
just at this stae of growth in this medium and at this temperature that the cultures
become filterable. And, just as had been anticipated, ordinary dark-field
examination revealed unchanged, long, actively motile bacilli; bacilli having
granules within their substance; and free-swimming, actively motile granules;
while under the Rife microscope were demonstrated the same long, unchanged,
almost colorless bacilli; bacilli, practically colorless, inside and at one end
of which was a turquoise-blue granule resembling the filterable forms of the
typhoid bacillus; and free-swimming, small, oval, actively
motile,turquoise-blue granules. By transplanting the cultures of the
filter-passing organisms or virus into a broth, they were seen to change over
again into their original rodlike forms.
At the same time that these findings of Drs. Rife and Kendall were confirmed by
Dr. Edward C. Rosenow, of the Mayo Foundation, the magnification with
accompanying resolution of 8,000 diameters of the Rife microscope, operated by
Dr. Rife, was checked against a dark-field oil-immersion scope operated by Dr.
Kendall and an ordinary 2-mm. oil-immersion objective, x 10 ocular, Zeiss scope
operated by Dr.Rosenow at a magnification of 900 diameters. Examinations of
gram and safranin-stained films of culture of Bacillus typhosus, gram and
safranin-stained films of blood and of the sediment of the spinal fluid from a
case of acute poliomyelitis were made with the result that bacilli,
streptococci, erythrocytes, polymorphonuclear leukocytes, and lymphocytes
measuring nine times the diameter of the same specimens observed under the
Zeiss scope at a magnification and resolution of 900 diameters, were revealed
with unusual clarity. Seen under the dark-field microscope were moving bodies
presumed to be the filterable turquois-blue bodies of the typhoid bacillus
which, as Dr.Rosenow has declared in his report (Observations on filter-passing
forms of Eberthella-typhi-Bacillus typhosus - and of the streptococcus from
poliomyelitis, Proc.Staff Meeting Mayo Clinic, July 13, 1932), were so
"unmistakably demonstrated" with Rife microscope, while under the
Zeiss scope stained and hanging-drop preparations of clouded filtrate culture
were found to be uniformly negative. With the Rife microscope also were
demonstrated brownish-gray cocci and diplococci in hanging-drop preparations of
the filtrates of streptococcus from poliomyelitis. These cocci and diplococci,
similar in size and shape to those seen in the culture although of more uniform
intensity, and characteristic of the medium in which they had been cultivated,
were surrounded by a clear halo about twice the width of that at the margins of
the debris and of the Bacillus typhosus. Stained films of filtrates and
filtrate sediments examined under the Zeiss microscope, and hanging-drop,
dark-field preparations revealed no organisms, however. Brownish-gray cocci and
diplococci of the exact same size and density as those observed in the
filtrates of the streptococcus cultures were also revealed in hanging-drop
preparations of the virus of poliomyelitis underthe Rife microscope, while no
organisms at all could be seen in either the stained films of filtrates and
filtrate sediments examined with the Zeiss scope or in hanging-drop
preparations examined by means of the dark-field. Again using the Rife
microscope at a magnification of 8,000 diameters, numerous nonmotile cocci and
diplococci of a bright-to-pale pink in color were seen in hanging-drop
preparations of filtrates of Herpes encephalitic virus. Although these were
observed to be comparatively smaller then the cocci and diplococci of the
streptococcus and poliomyelitis viruses, they were shown to be of fairly even
density, size and form and surrounded by a halo. Again, both the dark-field and
Zeiss scopes failed to reveal any organisms, and none of the three microscopes
disclosed the presence of such diplococci in hanging-drop preparation of the
filtrate of a normal rabbit brain. Dr. Rosenow has since revealed these
organisms with the ordinary microscope at a magnification of 1,000 diameters by
means of his special staining method and with the electron microscope at a
magnification of 12,000 diameters. Dr. Rosenow has expressed the opinion that
the inability to see these and other similarly revealed organisms is due, not
necessarily to the minuteness of the organisms, but rather to the fact that
they are of a nonstaining, hyaline structure. Results with the Rife
microscopes, he thinks, are due to the "ingenious methods employed rather
than to excessively high magnification." He has declared also, in the
report mentioned previously, that "Examination under the Rife microscope
of specimens containing objects visible with the ordinary microscope, leaves no
doubt of the accurate visualization of objects or particulate matter by direct
observation at the extremely high magnification obtained with this
instrument."
Exceedingly high powers of magnification with accompanying high powers of
resolution may be realized with all of the Rife microscopes, one of which,
having magnification and resolution up to 18,000 diameters, is now being used
at the British School of Tropical Medicine in England. In a recent
demonstration of another of the smaller Rife scopes (May 16, 1942) before a
group of doctors including Dr. J.H. Renner, of Santa Barbara, Calif.; Dr. Roger
A. Schmidt, of San Francisco, Calif.; Dr. Lois Bronson Slade, of Alameda,
Calif.; Dr. Lucile B. Larkin, of Bellingham, Wash.; Dr. E. F. Larkin, of
Bellingham, Wash.; and Dr. W. J. Gier, of San Diego, Calif., a Zeiss ruled
grading was examined, first under an ordinary commercial microscope equipped
with a 1.8 high dry lens and X 10 ocular, and then under the Rife microscope.
Whereas 50 lines were revealed with the commercial instrument and considerable
aberration, both chromatic and spherical noted, only 5 lines were seen with the
Rife scope, these 5 lines being so highly magnified that they occupied the
entire field, without any aberration whatsoever being apparent. Dr. Renner, in
a discussion of his observations, stated that "The entire field to its
very edges and across the center had a uniform clearness that was not true on
the conventional instrument." Following the examination of the grading, an
ordinary unstained blood film was observed under the same two microscopes. In
this instance, 100 cells were seen to spread throughout the field of the
commercial instrument while but 10 cells filled the field of the Rife scope.
The universal microscope, of course, is the most powerful Rife scope,
possessing a resolution of 31,000 diameters and magnification of 60,000
diameters. With this it is possible to view the interior of the 'pin-point'
cells, those cells situated between the normal tissue cells and just visible
under the ordinary microscope, and to observe the smaller cells which compose
the interior of these pin-point cells. When one of these smaller cells in
magnified, still smaller cells are seen within its structure. And when one of
the still smaller cells, in its turn, is magnified, it, too, is seen to be
composed of smaller cells. Each of the 16 times this process of magnification
and resolution can be repeated, it is demonstrated that there are smaller cells
within the smaller cells, a fact which amply testifies as to the magnification
and resolving power obtainable with the universal microscope.
More then 20,000 laboratory cultures of carcinoma were grown and studied over a
period of 7 years by Dr. Rife and his assistants in what, at the time, appeared
to be a fruitless effort to isolate the filter-passing form, or virus, which
Dr. Rife believed to be present in this condition. Then, in 1932, the reactions
in growth of bacterial cultures to light from the rare gasses was observed,
indicating a new approach to the problem. Accordingly, blocks of tissue
one-half centimeter square, taken from an unulcerated breast carcinoma, were
placed in a circular glass loop filled with argon gas to a pressure of 14
millimeters, and a current of 5,000 volts applied for 24 hours, after which the
tubes were placed in a 2-inch water vacuum and incubated at 37 degrees C. for
24 hours. Using a specially designed 1.12 dry lens, equal in amplitude of
magnification to the 2-mm. apochromatic oil-immersion lens, the cultures were
then examined under the universal microscope, at a magnification of 10,000
diameters, where very much animated, purplish-red, filterable forms, measuring
less then one-twentieth of a micron in dimension, were observed. Carried
through 14 transplants from K Medium to K Medium, this B. X. virus remained
constant; inoculated into 426 Albino rats, tumors "with all the true
pathology of neoplastic tissue" were developed. Experiments conducted in
the Rife Laboratories have established the fact that these characteristic
diplococci are found in the blood monocytes in 92 percent of all cases of
neoplastic diseases. It has also been demonstrated that the virus of cancer,
like the viruses of other diseases, can be easily changed from one form to
another by means of altering the media upon which it is grown. With the first
change in media, the B. X. virus becomes considerably enlarged although its
purplish-red color remains unchanged.
Observation of the organism with an ordinary microscope is made possible by a
second alteration of the media. A third change is undergone upon asparagus base
media where the B. X. virus is transformed from its filterable state into
cryptomyces pleomorphia fungi, these fungi being identical morphologically both
microscopically to that of the orchid and of the mushroom. And yet a fourth
change may be said to take place when this cryptomyces pleomorphia, permitted
to stand as a stock culture for the period of metastasis, becomes the
well-known mahogany-colored Bacillus coli.
It is Dr. Rife's belief that all micro-organisms fall into 1 of not more than
10 individual groups (Dr. Rosenow has stated that some of the viruses belong to
the group of the streptococcus), and that any alteration of artificial media of
slight metabolic variation in tissues will induce an organism of one group to
change over into any other organism included in that same group, it being
possible, incidentally, to carry such changes in media or tissues to the point
where the organisms fail to respond to standard laboratory methods of
diagnosis. These changes can be made to take place in as short a period of time
as 48 hours. For instance, by altering the media - 4 parts per million per
volume - the pure culture of mahogany-colored Bacillus coli becomes the
turquoise-blue Bacillus typhosus. Viruses of primordial cells of organisms
which would ordinarily require an 8-week incubation period to attain their
filterable state, have been shown to produce disease within 3 days' time,
proving Dr. Rife's contention that the incubation period of a micro-organism is
really only a cycle of reversion.
He states:
"In reality, it is not the bacteria themselves that produce the disease,
but we believe it is the chemical constituents of these micro-organisms
enacting upon the unbalanced cell metabolism of the human body that in
actuality produce the disease. We also believe if the metabolism of the human
body is perfectly balanced or poised, it is susceptible to no disease."
In other words, the human body itself is chemical in nature, being comprised of
many chemical elements which provide the media upon which the wealth of
bacteria normally present in the human system feed. These bacteria are able to
reproduce. They, too, are composed of chemicals. Therefore, if the media upon
which they feed, in this instance the chemicals or some portion of the
chemicals of the human body, become changed from the normal, it stands to
reason that these same bacteria, or at least certain numbers of them, will also
undergo a change chemically since they are now feeding upon media which are not
normal to them, perhaps being supplied with too much or too little of what they
need to maintain a normal existence. They change, passing usually through
several stages of growth, emerging finally as some entirely new entity - as
different morphologically as are the caterpillar and the butterfly (to use an
illustration given us). The majority of the viruses have been definitely
revealed as living organisms, foreign organisms it is true, but which once were
normal inhabitants of the human body -living entities of a chemical nature of
composition.
Under the universal microscope disease organisms such as those of tuberculosis,
cancer, sarcoma, streptococcus, typhoid, staphylococcus, leprosy, hoof and
mouth disease, and others may be observed to succumb when exposed to
certain lethal frequencies, coordinated with the particular frequencies peculiar to each
individual organism, and directed upon them by rays covering a wide range of
waves. By means of a camera attachment and a motion-picture camera not built
into the instrument, many "still" micrographs as well as hundreds of
feet of motion-picture film bear witness to the complete life cycles of
numerous organisms. It should be emphasized, perhaps, that invariably the same
organisms refract the same colors. when stained by means of the monochromatic
beam of illumination of the universal microscope, regardless of the media upon
which they re grown. The virus of the Bacillus typhosus is always a turquoise
blue, the Bacillus coli always mahogany colored, the Mycobacterium leprae always
a ruby shade, the filter-passing form of virus of tuberculosis always an
emerald green, the virus of cancer always a purplish red, and so on. Thus, with
the aid of this microscope, it is possible to reveal the typhoid organism, for
instance, in the blood of a suspected typhoid patient 4 and 5 days before a
Widal is positive. When it is desired to observe the flagella of the
typhoid-organism, Hg salts are used as the medium to see at a magnification of
10,000 diameters.
In the light of the amazing results obtainable with this universal microscope
and its smaller brother scopes, there can be no doubt of the ability of these
instruments to actually reveal any and all microorganisms according to their
individual structure and chemical constituents.
With the aid of its new eyes - the new microscopes, all of which are
continually being improved - science has at last penetrated beyond the boundary
of accepted theory and into the world of the viruses with the result that we
can look forward to discovering new treatments and methods of combating the
deadly organisms - for science dose not rest.
To Dr. Karl K. Darrow, Dr. John A. Kolmer, Dr. William P. Lang, Dr. L. Marton,
Dr. J. H. Renner, Dr. Royal R. Rife, Dr. Edward C. Rosenow, Dr. Arthur W. Yale,
and Dr. V. K. Zworykin, we wish to express our appreciation for the help and
information so kindly given us and to express our gratitude, also, for the
interest shown in this effort of bringing to the attention of more of the
medical profession the possibilities offered by the new microscopes.