Royal Rife Answers Questions During John Cranes Trial

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" Bil Green " <magpulser

Sun, 8 Oct 2006 01:16:30 -0700

[rife-list] Royal Rife Answers Questions During John Cranes Trial

 

 

 

 

Questions that were sent to Royal Rife while he was in Mexico to answer

 

 

 

 

Answers to the above questions. These were sent back to Cranes Lawyer

from Mexico

 

 

 

1. Please state your name?

 

Royal Raymond Rife

 

2. Where do you reside?

 

As a tourist in Tijuana

 

3. Is it your intention to attend as a witness at the trial of this

action?

 

No

 

4. Are you the same Royal R. Rife who invented the system of

killing or de-activating pathogenic organisms by electronic waves or

frequencies produced by instruments similar to those made by Mr. John

Crane, one of the Defendants in this case?

 

Yes

 

5 If so, when did you begin your experimental work on this system?

 

1915

 

6. How long a period did your work cover, in developing the device

and the techniques of its use?

 

From 1920 to the present time - 40 years and development is still

continuing.

 

7. What is the basic theory upon which you sought to find a means of

killing pathogenic organisms?

 

The theory of coordinative resonance with frequencies which I proved

would kill microorganisms by electron

transfer and internal stresses of pathogenic cells owing to

electromagnetic and electrostatic forces.

 

8. What kind of pathogenic organisms did you study, in these experiments?

 

Tetanus, typhoid, gonorrhea, syphilis, staphylococci, pneumonia,

strertothrix, streptococi, tuberculosis, sarcoma, carcinoma,

leprosy, polio, cholera, actinomycosis, glanders, bubonic plague,

anthrax, influenza, herpes, cataracts, glaucomia, colitis, sinus,

ulcers and many other virus bacteria, and fungi.

 

9. From what sources were these organisms obtained?

 

The Hooper Foundation, Paradise Valley Sanatorium, from Northwestern

Medical University in Chicago, from the Mayo Clinic, and from many

medical doctors.

 

10. What sort of laboratory facilities did you have, for use in these

experiments?

 

I had one of the best privately equipped laboratories in the world

complete with a million volt X-Ray,

frequencyinstruments, electronic test equipment, precision lathes,

mills, drill presses, shaper and all equipment

necessary to make instruments, microscopes, glass blowing, and a

surgical room for animals with sterilizers of the steam type and a

pathology room complete with microscopes of all types virus

microscopes which I had designed and built for the isolation of

cancer virus, T.B. virus, typhoid virus and many other virus. I had a

stop motion microscope set up for the life study of microorganisms

from the cradle to the grave. I had animals in cages in the basement

with facilities for 1000 animals. The Rife Research Laboratory was

air-conditioned and humidity controlled to one tenth of one degree.

 

11. Where was your laboratory located?

 

On Alcott Street across the bridges mansion in Point Loma

 

12. Did you study viruses, among other pathogenic organisms?

 

Yes.

 

13. Were any special instruments required for your study of viruses?

 

Yes.

 

14. What were they?

 

Prismatic virus microscopes and Berkefelt porcelain filters, a

micromanipulator and electronic test instruments and frequency

instruments.

 

15. Were all of these obtained from ordinary commercial sources?

 

No - I could not buy them on the open market and they are still not

obtainable even today.

 

16. If some were not obtainable from ordinary commercial sources, how

did you obtain them?

 

I had to design and build these instruments to accomplish what I

wanted to attain with my research.

 

17. Who designed these?

 

I designed them.

 

18. Where were they made?

 

In the Rife Research Laboratory.

 

19. Describe these special instruments for us?

 

The universal microscope was described and published by the journal of

the Franklin Institute. Time does not permit me to describe all of the

many instruments that I designed and constructed. The micromanipultor

was used to dissect and operate on cells. The spectrometer was used to

measure the angle of crystals, the frequency instruments were used to

kill bacteria, virus, and fungi, the microscopes of the prismatic

virus were used to study living virus, bacteria, and fungi, a

petrographical micropolariscope was used to analyze chemicals and

color frequencies with polarized light, special rare gas glass

contained atmospheres were used to provide ionized radiation to

transmit energy to increase virulence and to devitalize all

microorganisms as desired.

 

20. Which pathogenic organisms did you study in virus form?

 

Cancer virus, typhoid, tuberculosis virus, herpes virus, B-coli virus,

poliomyelitis virus, and about 40 other viruses that have never been

isolated before.

 

21. How did you obtain these viruses?

 

From pure cultures of known and medical diagnosed tissues of human

disease filtered through porcelain Berkefeld filters.

 

22. Describe your experiments by which you isolated these viruses?

 

After the filtered form was obtained, a micropipette is used to place

a drop of the fluid on a slide. This slide is placed on the

microscope stage of any of the 5 virus microscopes that I designed and

built. A special Bisely prism which works on a counter rotation

principle selects a portion of the light frequency which illuminates

these virus in their own characteristic chemical colors by emission

of coordinative light frequency and the virus become readily

identifiable by the colors revealed on observation. 8000 to 17000x

magnification is sufficient to see them. Before building the virus

prismatic microscopes, I sectioned over 15,000 slides trying all

types of acid and aniline dye strains with no results over a period of

10 years.

 

23. How did you determine whether these viruses were pathogenic?

 

By animal tests and from known sources and by microscope examination

which reveals the true identity of microorganisms to the trained

observer.

 

24. Describe your experiments made to prove that these viruses were

pathogenic?

 

On one series of cancer tests, I inoculated the virus which I had

isolated and filtered from an unulcerated breast mass into an Albino

rat, the tumor was allowed to grow and then I surgically removed the

tumor and again isolated and filtered the virus from a portion of the

ground up tumor and inoculated the next rat and repeated this

procedure 411 times to prove that this virus was the causative agent

of cancer. Tests on many other diseases such as those previously

mentioned are too numerous to even start on at this time.

 

25. About how long a period of time did your work/study of these

viruses, and proof of their pathogenic character, over?

 

15 years on virus only

 

26. Did you also study bacterial forms of pathogenic organisms

associated with these viruses?

 

Yes.

 

27. Did you find whether some bacteria were capable of releasing a

form of virus?

 

Yes. Virus are released from bacteria just as a chicken lays an egg.

 

28. How did you determine this?

 

By virus observation and cell study and virus photographs which I made

and one which John Crane made from a film of cancer virus which has

been copyrighted.

 

29. What are some of the bacteria which you found to be capable of

releasing a form of virus?

 

Bacillus coli, tuberculosis, typhoid, and many others.

 

30. Were certain kinds of culture media better suited than others to

the study of the relationship between thebacteria and virus forms?

 

A media developed by Arthur I. Kendall known as " K " media proved

superior to other types of bacteria media.

 

31. If so, why, or in what way, were some culture media superior to

others for this purpose?

 

Because of the results obtained.

 

32. Were any physicians or scientists associated with you in any of

these studies?

 

Yes

 

33. Who were they?

 

Milbank Johnson, M.D., Arthur I. Kendall, Ph.D., E.C. Rosenow, M.D.,

Coolidge of General Electric, O.C. Grunner,

M.D., Henry Siner, Dr. Copp, M.D., Alvin G. Foord, M.D., Ernest

Lynwood Walker, M.D., and Karl Meyer,

M.D., of the Hooper Foundation of San Francisco, George Dock,

M.D.,Waylen Morrison, M.D., Dr. Fischer, M.D.,

Verne Thompson, Ben Cullen, Ray Lounsberry, M.D., James B. Couche,

M.D., Charles F. Tully, D.D.S., Arthur Yale, M.D., R.T. Hamer, M.D.,

John Crane, Dave Sawyer, Don Tully, J. Heitger, M.D., Royal Lee,

Ph.D., T.O. Burger, M.D., Alice Kendall and many others.

 

34. Where did they work with you?

 

Work was conducted in various laboratories, offices, and buildings in

San Diego and in the United States. I traveled all over the world and

many doctors and scientists and executives visited me at my various

laboratories including the Rife Research Laboratory, The Point Loma

Lab set up at Dr. Tully's, The Rife Virus Microscope Institute, and

another microscope and dark room facility at San Diego, and I

furnished free of charge to the police crime laboratory thousands of

dollars worth of chemicals, precision instruments, electronic

instruments, and training in microscope techniques and laboratory

diagnosis and other equipment and glassware after I closed the Rife

Research Laboratory in 1946. Another laboratory for research work on

seawater conversion was set up and used at the foot of Canyon Street

in Point Loma.

 

35. What part did they have in any of these experiments or studies?

 

Initially the work and the origin was developed under my control and

guidance. Later their work became an interest of collaboration and

observation of the results attained. Initially I worked with loose

couplers to get an audio oscillation and then with the use of

transmitters, I tried to balance the audio and modulate the audio on a

carrier wave to transmit the audio energy but I found that both the

audio and the audio transmitted through a tube as an antenna worked

equally as well in a painless and harmless method to human tissue.

Coolidge furnished many tubes. Milbank Johnson, a multimillionaire,

setup and supervised three human research clinics. The first clinic

was set up under a special medical research committee of the

University of Southern California with Dr. Rufus B. von Klein Smidt on

the committee in the home of Ellen Scripps in La Jolla in 1934.

Johnson selected outstanding doctors to aid us in the clinical work

such as Docks, Morrison, Foord, Meyer, Kendall, Rosenow, Fischer of

the Children's Hospital in New York, and others helping or observing

were Heitger, Lounsberry, Copp, Alice Kendall, Henry Seiner, Grunner,

Burger, Hamer, Couche, Yale, and Cullen. Walker and I studied leprosy

and I isolated a virus which we jointly demonstrated was common to

rat, soil, and human leprosy and I found a frequency which would

eliminate leprosy. Dr. Gonin M.D. visited me and I sent Henry Siner to

demonstrate a virus microscope in England to the medical profession

there. Alice Kendall worked for me in the lab and so did Henry Seiner

and others. From 1950 and on, John Crane has continued on with this

research. The others were visitors and interested parties. Many

others have aided in promotion of this research and the AMA has

suppressed all effort and research knowledge of my developments.

 

36. Did you grow bacteria and viruses in various culture media?

 

Yes

 

37. How did you determine what they were?

 

They can readily be diagnosed by their own true colors which are

emitted when placed in any of the five virus microscopes that I

designed and built for this virus identification and study.

 

38. What study and experience did you have in the science of optics,

before commencing these experiments?

 

I studied for 6 years with Hans Luckel who was Carl Zeiss's optical

scientist and researcher. I also made all the

photomicrographs for the Atlas of Parasites which was done at the

University of Heidelberg. I also studied eye surgery for two years.

 

39. Over about what period of time had you made such study and gained

this experience?

 

Nine years before commencing on my own research.

 

40. Did you find ordinary microscopes, such as are obtainable from

commercial sources, adequate for the study of these viruses?

 

No

 

41. In what ways were they deficient?

 

They have insufficient power, poor detail and definition, and poor

resolution and cannot illuminate the virus with selective frequency

or frequencies of monochromatic beam light which is required to see

virus control of the light is very important.

 

42. What types of microscope did you find necessary to complete your

study of these viruses?

 

Prismatic virus microscopes which I designed and built for virus study

and research only. I have never tried to

commercialize on these instruments. They were offered to Baush and

Lomb but they couldn't justify the cost of tooling to build these

complex instruments and the doctors could not afford to buy them

either because they would have been too expensive for the average

laboratory to even consider.

 

43. In what ways did they differ from the commercially available types?

 

In the barrel were prisms which transmitted the light. The stage had

to be leveled and a series of condenser lenses between the patented

microscope lamp of mine and the Risely prism were located below the

stage. Special lens spacings were important to compensate for the

extra long tube length of 220 and 440 mm and a higher degree of

accuracy in stage adjustments was provided. In the Universal

Microscope, 7 turns of the dial moved the object under study one

micron. Slit ultra illumination was also provided.

 

44. Did you obtain the kinds of special microscopes you found to be

necessary?

 

Yes

 

45. How did you obtain them?

 

I built many and I purchased some and had them built to my specifications.

 

46.What types were they?

 

Standard research types, prismatic virus types, crystallographic,

petrographical-micropolariscope, polarized, and historical types.

 

47.What did these special microscopes do which the commercially

available types would not do as well?

 

Show virus and allow us to study them alive and identify them as virus

and allow us to diagnose them as to the disease of which they caused

and were associated.

 

48.What is necessary, in order to make bacteria and viruses visible

under the microscope?

 

First there must be high enough power to enable the observer to see

them and second they must be identified by a frequency of light which

coordinates with the chemical constituents of the virus or filterable

form in question. To my knowledge there is only one instrument today

which will even show these virus and that is the Rife prismatic virus

microscopes which I built for this work. The electron microscope is a

useless device for this study because the virus are killed instantly

and you don't know what form you are seeing them in and generally

appear as round balls of dried up chemical particles.

 

49.What different methods of staining bacteria and viruses are in

common use?

 

Acid and analine dye strains of many formulae are commercially available.

 

50. Did you find these common methods of staining sufficient for the

experiments you performed?

 

No

 

51. If not, what were their deficiencies?

 

They would not show the flagella, or the virus.

 

52. Did you devise another method of staining or making visible

bacteria and viruses?

 

Yes

 

53. What was this method?

 

I had devised a stain with Alfalfa hay and mercury for flagella on

B-Coli and typhoid to count their concentration. Virus were made

visible for the first time with a variable light frequency controlled

by a Risely prism of a counter-rotating nature, an iris diaphragm,

condenser lenses and other features previously mentioned.

 

54. Explain how it was done?

 

By rotation and variable monochromatic beam adjustment of the Rife

prismatic virus microscopes.

 

55. How did you obtain the instruments necessary to do this?

 

I built them in my research laboratory. Which is shown in movies that

John Crane has at RVMI.

 

56. What study and experience have you had in the science of

Bacteriology?

 

I studied bacteriology at John Hopkins University and the University

of Heidelberg and in my own research laboratory.

 

57. Over about what period of time did you get this study and experience?

 

40 years

 

58. Besides studying bacteria and viruses growing in culture media,

did you also make any study of their effects upon laboratory animals

inoculated with such bacteria or viruses?

 

Yes

 

59.What kinds of animal were used in such experiments?

 

Albino rats, Guina pigs, rabbits. I had about 800 rats which were used

constantly.

 

60.Where were such experiments performed?

 

In the Rife Research Laboratory in Point Loma.

 

61. Under whose direction?

 

Under my direction.

 

62. Did any other scientists or physicians assist you in any of these

studies of inoculated laboratory animals?

 

No, but I had men that worked for me and helped me.

 

63. Did any other scientists observe, without actually assisting, any

of these studies or experiments?

 

Yes. Dr. Kendall, Grunner, Johnson, Couche, Copp, Lounsberry, Burger,

Seiner, Cullen, Foord, Rosenow, Karl Meyer,

Walker, and others as stated before.

 

64. Who were they?

 

(Blank)

 

65.What part did they take in such studies?

 

By bringing cancer tissue, collaborating results, by using the virus

microscopes and observing my results and observations, by growing

virus and by conducting clinical tests on virus, bacteria and fungi on

cultures and human cases or patients for their own research and knowledge.

 

66. As a result of such studies, did you and Dr. Arthur I. Kendall

publish a report of some of your experiments or studies of filterable

forms of Bacillus Typhosus?

 

Yes

 

67.Was this report published in " California and Western Medicine " , the

journal of the California Medical

Association, in the December, 1931, issue?

 

Yes

 

68. Is this a copy of the article ? (Attach as Defendant's Exhibit A)

 

Yes

 

69. Was this Dr. Arthur Isaac Kendall, Ph. D., at that time the of Medical Research of Northwestern University Medical School?

 

Yes

 

70. In July, 1932, did you continue some of this study of bacteria

and viruses with Dr. Isaac Kendall in his laboratory at Northwestern

University Medical School?

 

Yes

 

71. At that time, did Dr. E. C. Rosenow, M.D., of the Division of

Experimental Bacteriology of the Mayo Clinic, Rochester, Minnesota,

observe some of this study made at Northwestern University Medical

School, in Dr. Kendall's laboratory?

 

Yes

 

72. Did Dr. Rosenow publish a report of this study in the July 1932

issue of the Mayo Clinic bulletin?

 

Yes

 

73. Is this a copy of this publication of Dr. Rosenow's article

(Attach as Defendant's Exhibit B)

 

Yes.

 

74. About when did you begin your experiments in the effect of

electronic frequencies upon bacteria and viruses?

 

1920

 

75. How did you obtain the device or mechanism used to generate such

frequencies?

 

Some coils I wound myself. Other parts I purchased.

 

76. How did you determine whether particular frequencies had any

affect upon bacteria or viruses?

 

By observation with bacteria and virus under the Rife virus prismatic

microscopes in conjunction with the application of electronic energy.

 

77. Were you able to kill or de-activate any bacteria or viruses by

the application to them of electronic currents or

rays?

 

Yes

 

78. Can you name some of the bacteria and viruses which you were able

to kill or de-activate by such means?

 

Tetanus, typhoid, gonorrhea, treponema pallidum, staphylococci,

pneumonia, streptothrix, bacillus coli, tuberculosis, streptococci,

sarcoma, carcinoma, and many others. It was found that by using

combinations of these frequencies for the different microorganisms

that many other disease could be helped like sinus, ulcers, cataract,

arthritis, poliomyelitis, etc.

 

79. Is there a distinction between the terms " kill " and " de-activate "

as you have used them? That is to say, were any of these viruses or

bacteria deprived of their virulent activity without having to

completely kill them?

 

Yes. On some research it was found that after transfer to another

media no further reproduction would occur.

 

80. After treatment of viruses or bacteria by the application to them

of certain electronic currents or rays, as you have mentioned, was

there ever any change in the appearance of such bacteria or viruses

as seen under your microscope? If so, describe it.

 

Yes. Some types will explode or disintegrate and some will gather

together like log jams or agluetinate.

 

81. Were you acquainted with Dr. Milbank Johnson, M. D., during this

period?

 

Yes

 

82. Did he participate in any of your experiments or studies on the

effect of electronic frequencies upon bacteria and viruses?

 

Yes

 

83. Did he participate in any of your experiments or studies on the

effect of these electronic frequencies upon laboratory animals which

had been inoculated with various diseases?

 

Yes

 

84. Did you furnish one of your electronic frequency-generators to

Dr. Milbank Johnson for his use?

 

Yes

 

85. Over about what period of time did he use it?

 

8 years

 

86. Where did he make use of it?

 

In the Santa Fe hospital in Los Angeles and a private clinic in Pasadena.

 

87. Was this electronic frequency-generator used by him or under his

direction in the treatment of diseases of human patients?

 

Yes

 

88. Did he report to you the result of these treatments?

 

Yes

 

89. Did you observe the giving of any of these treatments?

 

Yes

 

90.Did you observe the results of these treatments?

 

Yes

 

91.What changes did you observe in the condition of any of the

patients so treated by Dr. Milbank Johnson with the instrument you

had furnished to him? Describe them in detail?

 

I observed some cataract cases, etc.

 

92.During the period of time when Dr. Milbank Johnson was so using

your electronic frequency-generator, were you acquainted with Dr.

James B. Couche M. D. (now deceased)?

 

Yes

 

93. Did Dr. James B. Couche participate in the work of Dr. Milbank

Johnson in the treatment of human patients with the frequency-generator?

 

Yes

 

94. Did you furnish Dr. James B. Couche, M. D., with one of your

electronic frequency-generators for his own use?

 

Yes. The beam Ray Corporation built two instruments for Dr. Couche.

 

95.When did Dr. Milbank Johnson die?

 

1942

 

96.Was the work of Dr. Milbank Johnson in treating human patients

with your frequency-generator continued after his death?

 

Yes

 

97.Did Dr. James B. Couche continue to use the frequency-generator

which you had furnished to him? If so, until about what date?

 

Yes. Until he died in 1959.

 

98.About when did Dr. James B. Couche die?

 

In the spring of 1959.

 

99. Did Dr. James B. Couche report to you the results of his use of

your electronic frequency-generator?

 

Yes

 

100. Did you observe any of the treatments given by Dr. James B.Couche

with your electronic

frequency-generator?

 

Yes

 

101. Did you observe the results of any of the treatments given by

Dr. James B. Couche with your electronic frequency-generator?

 

Yes

 

102.What changes did you observe in the condition of any of the human

patients who had been so treated with your frequency-generator by Dr.

James B. Couche?

 

I saw cancer and tuberculosis cases that had completely recovered. I

saw Dr.Couches brother who had come over from England. He had a 30

year sinus condition with terrible drainage. Dr. Couche used the

frequency instrument on him and he was well in three weeks. Dr. Couche

had treated Dr. Hamer, M.D. for a sinus condition which cleared up.

Dr. Couche had treated Dr. Butterfield, M.D's brother-in-law who had a

stiff wrist * a tuberculosis of the bone which cleared up. Also I saw

a mexican boy who had osteomelitys of the bone which Dr. Couche

cleared up with the frequency instrument. I saw George Lemm being

treated by Dr. Couche for tuberculosis and he had come out from

Chicago to die. He was sent from the Vulclain home. As soon as they

found out that Couche was getting results, they tried to get all of

their patients back but Lemm said no that he was going to finish up

with Couche and he completely recovered.

 

103. Did you furnish Dr. Arthur W. Yale, M. D. (now deceased) with one

of your electronic frequency-generators? If so, about when?

 

Yes. He ordered an instrument from the Beam Ray Corporation in 1937.

 

104. Did Dr. Arthur W. Yale furnish you with any reports of the

results of his treatment of human patients with your electronic

frequency-generator device?

 

Yes

 

105. Did you observe the results of any of the treatments given by

Dr. Arthur W. Yale?

 

Yes

 

106.Did you observe the condition of any of Dr. Arthur W. Yale's

patients after they had been treated by him with your electronic

frequency-generator? If so, what change, if any, in their condition

did you observe?

 

Yes. They completely recovered from syphilis, cancer, tuberculosis,

and many other infections .

 

107.Did you perform any experiments on laboratory animals which had

been inoculated with any diseases, to determine the affect upon such

animals of treatment with your electronic frequency-generator?

 

Yes

 

108. What kind of animals did you use?

 

Albino rats, rabbits, Guina pigs.

 

109. With what diseases were these animals inoculated?

 

Sarcoma, carcinoma, tuberculosis, typhoid, etc.

 

110. Were any of these animals inoculated with cancer in any form?

 

Yes

 

111. Describe in detail the experiments with your electronic

frequency-generator?

 

Before the animal was inoculated a quarantine period of two weeks was

observed with stool analysis and metabolism check up made to be sure

that the animal was free of disease and in good health. On one series

of cancer tests I inoculated the cancer virus that I isolated from an

unulcerated human breast mass into an Albino rat and grew the tumor. I

surgically removed this tumor and again isolated the virus and

inoculated the next rat. I did this 411 times on one series of tests

to prove that the BX or the virus which I had isolated was in reality

the causative agent of cancer. This procedure is shown in a

documentary film which John Crane has of this work and it also shows

the virus of cancer before and after devitalization with a Rife

frequency instrument. An air bubble is shown coming into the cover

slip because I had not sealed it. We also did a great deal of work on

tuberculosis with animals and proved that the rod form and the virus

form must both be devitalized to attain results which requires two

frequencies * One for each form before recovery can occur. The

treatment for all of the diseases proved successful and hundreds of

tests were conducted on each disease with adequate controls before

the critical frequencies were established.

 

112. Did you compare the subsequent condition of the animals so

treated with your frequency-generator with the condition of " control "

animals which had been inoculated with disease but not treated with

your frequency-generator? If so, describe the difference, if any,

which you observed in their condition.

 

Yes. The inoculated controls died and the controls which were not

inoculated were not affected.

 

113. About how many experiments of this kind did you make?

 

50,000 [note: on the original document 100,000 had been type-written,

crossed out and 50,000 added by hand] animal tests and 400 [15,000

type-written, crossed out and 400 written by hand] test tubes daily

on my experiments.

 

114. Over about what period of time did you conduct these experiments?

 

26 years

 

115. Did you find, from these experiments, that it made any difference

which particular frequency you used in the treatment of any certain

disease?

 

Yes

 

116. Did any disease respond exactly the same to all frequencies or a

wide variety of frequencies? If so, which one?

 

No

 

117. Were you able to determine whether each kind of bacteria or

virus which you tested was affected most by some particular frequency?

 

Yes

 

118. What happened when you used a different frequency on it?

 

It was not affected.

 

119. Did you make a moving picture showing the interior of your

laboratory and some of its equipment?

 

Yes

 

120. Did this moving picture also show some of your experimental

work on laboratory animals?

 

Yes. Some cancer work is shown.

 

121. In this moving picture, who is the person shown performing

surgical operations on laboratory animals?

 

I performed all surgery at the Rife Research Laboratory.

 

122. Who now has this moving picture? Did you give it to him?

 

John Crane. Yes

 

123.Did you ever explain to John F. Crane, one of the defendants in

this case, the principles upon which your electronic

frequency-generator is used in the treatment of diseases?

 

Yes in 1950.

 

124. Did you also inform him of the particular frequencies which you

had found to be effective in the treatment of various diseases?

 

Yes. Verne Thompson and I gave the frequencies to John Crane.

 

125. When did you furnish him with this information?

 

In 1950.

 

126. Did you ever request any governmental department or agency to

make a test of your electronic

frequency-generator to determine its effect upon diseases? If

so, which one or ones?

 

Yes. The Department of Health, Education and Welfare and the National

Research Council * Committee on Growth *Washington D.C., The American

Cancer Society, The Damon Runyon Fund, The Slone Kettering Institute,

The International Cancer Clinic and many others. They have shown no

interest in an electronic method.

 

127.Did any one of them express willingness to make such a test, or

even to observe such a test? Is so, which one?

 

Yes. The American Cancer Society was interested until they found out

that John Crane and I are not medical doctors and then they called

John Crane from New York and stated that they had decided to cancel

the proposed project which would have shown them how to isolate the

virus, make it virulent, grow the cancer tumors and how to

electronically eliminate the cancer. They spend millions on drugs but

nothing on electronics unless it will supplement drugs like X-Ray and

radioactive treatments which put terrible scar tissue and burns

inside the body and then the person has to have a great amount of

dope and pain killers to keep the pain down. The drug racketeer makes

ten billion dollars annually on cancer alone and with this money they

have been able to have an unconstitutional law put on the books which

stated that people will only be treated for cancer by medical doctors

with X-Ray, radioactive treatments, and surgery creating a drug

monopoly to kill cancer; slowly.

 

128. Did any one of them ever actually make a test of your

electronic frequency-generator, using the frequencies which you had

found to be effective, so far as you know?

 

No

 

129.Did you ever request any medical school to make a test of your

electronic frequency-generator, using the frequencies which you had

found to be effective?

 

Yes

 

130. Other than the work of the Special Committee under Dr. Milbank

Johnson, did any medical school express a willingness to make such a test?

 

Yes. Work was done at the Hooper Foundation of the University of

California and at Northwestern University Medical School in Chicago

by Ernest Lynwood Walker and Arthur I. Kendall.

 

131. Did you ever request any medical society to make a test of your

electronic frequency-generator, using the frequencies which you had

found to be effective? If so, which one or ones?

 

Yes. The American Medical Association .

 

132.Did any medical society express a willingness to make, or to

observe such a test?

 

No

 

133. So far as you know, has any medical society ever made a test

of your electronic frequency-generator, using the frequencies which

you had found to be effective?

 

No

 

134. Have you ever made or observed a test of the effect of the

electronic frequency-generators, of the type produced by John F.

Crane, one of the Defendants in this case? If so, tell us the kind of

test or tests, who made such a test or tests, and what result you

observed.

 

Yes. I saw the instrument kill earthworms., (bacillus coli and others.

I showed John Crane how to accomplish this work.) ()Added later to the

answers

 

 

135. Have you been awarded a Research Fellowship in Bio-Chemistry by

any nationally-known Institute for Scientific Research?

 

Yes

 

136. What is the name of it?

 

Andean Anthropological Expedition

 

137. Is this a copy of the award, together with a copy of the covering

letter or transmittal from the Andean Anthropological Expedition?

(Attach as Defendant's Exhibit C).

 

Yes