Microbe / parasite targets which
are rampant in the environment
The parasitic microbes / parasites listed in
1a) and 1b) are fairly common throughout much of the world. Humans
are quite susceptible to all of these microbes / parasites and regularly
contract infections of one or more of them. In general you can think
of multiples of tens of millions of people and or animals currently infected
with each listing of 1a) and 1b). Rife type technology can dispose
of these microbes / parasites easily and quickly. Let us move quickly
to end this needless suffering. Pick several microbes you would like
to find the lethal ultrasound frequencies for.
About half the viruses that infect plants and
animals have a outer coat (capsid) which has an intrinsic geometry as illustrated
in Figures 1A and 1B. In animals
the outer coat (capsid) of the virus is also covered with a bi-lipid layer
obtained from the infected
host cell from which the virus budded off of. Other virus types that
will not be talked about here have analogous or similar symmetries and
periodisities which make them also susceptible to easy disruption and distruction
from specific frequencies of ultrasound.
In Figure 2A
the black dots represent spheroid shaped large single protein molecules.
Usually two or more types of protein spheroids make up the virus capsid
coat. These large protein olecules are deformable and are elastic
in nature. Figures 2B and 2C
the periodically spaced, elastically coupled, closed on themselves protein
clump structures that are formed when Figure 2 is folded into an icosahedral
of Figure 1B.
When real viruses of the structural type as
illustrated in Figure 1B are in living tissue they are deformed into spheroids.
This is due to the interaction of the virus capsid with the environment.
The bi-lipid coat on the surface of the capsid has an affinity with water
and this tends to deform the capsid into a sphere with tension on its surface.
The capsid and its outer coat form a simi- permeable membrane and the phenomena
of osmotic pressure causes the capsid to expand and be under tension.
There are other hydrophobic and hydrophilic reactions that can cause and
contribute to capsid deformation. Figures 3A through F illustrate
The bonds between adjacent protein molecules
in the virus capsid coat are generally hydrogen bonds and these are relatively
weak chemical bonds. To a first approximation, we can treat each
protein clump (molecule) in the capsid coat as a simple harmonic oscillator
as illustrated in Figure 4C. Imagine in Figure
4C that the center of mass is a steel ball. Imagine that that
steel ball has two elastic cords attached to it and that the cords are
attached to the ceiling and floor respectfully. And furthermore,
the elastic cords are under some tension. Now imagine that the
ball is pulled back and then released. The ball will oscillate back
and forth at some constant frequency. If the tension is now increased
in the cords and the ball is again pulled back and let go, the ball will
again oscillate back and forth at a constant frequency, but now at a higher
In fact, the frequency of oscillation will vary approximately proportional
to the square root of the tension in the cords for small displacements
from equilibrium of the ball. If the ball is exposed to some small
rythmic driving force of the same frequency of oscillation that is natural
for the mass of the ball and the tension in the cords present, then the
amplitude (displacement from equilibrium) of oscillation will increase
until the energy release into the surrounding environment by the motion
of the ball and cords per oscillation cycle equals the energy being supplied
per cycle by the rhythmic force. However, the larger the amplitude
(displacement from equilibrium) of the oscillation, the larger the stress
on where the elastic cords are attached.
If the cords are not well secured to the ceiling or floor, the cords
may decouple before the system goes into equilibrium with the rhythmic
driving force. In the case of the periodically spaced, elastically
coupled, and closed-on-themselves virus capsid sub-structures seen in Figure
4A, the "floor " and "ceiling" connections are weak hydrogen bonds between
adjacent protein clumps of the virus capsid. Figure 4E illustrates
the most stressful standing wave oscillation mode on a ten member protein
clump ring. In this oscillation mode, adjacent protein clumps are
oscillating 180 degrees out of phase, that is, as one protein clump is
moving upward from its equilibrium position, the adjacent clumps are moving
downward and visa versa. This type of oscillation mode puts maximum
tension / stress on the weak hydrogen bonds holding the protein clumps
to each other. At some relatively small displacement amplitude, the hydrogen
bonds will fail and the ring /capsid coat will disintegrate. Rife
observed viruses exploding like little hand grenades when they were exposed
to their mortal oscillation rate (MOR).
Figures 5B, C, and D illustrate several
standing wave oscillation modes that a ten member protein clump ring can
support. Maximum stress / tension occurs at the location of standing
wave nodes and the weakest regions on the protein clump ring is where the
clumps bond together with mainly hydrogen bonds. That is approximately
half way between
adjacent protein clump centers of mass. Therefore, we see that the
oscillation modes illustrated in Figures 5B and D are very destructive
where as that of 5C is only marginally destructive.
Figures 6A and B illustrate two more
very simple virus capsid coats. By following the instructions and
building the capsid coat models, you can see how many types of periodically
spaced, closed-on-themselves protein clump structures you find and also
how many overlapping and tangential closed protein clump structures you
Needed Equipment to Accomplish
a) Microscope with TV camera
b) B & K 10 MHz sweep function generator
c) VCR with time readout on video tape capability
d) Sweep controller box (see Alteronics below)
e) Ultrasound transducer that mounts on microscope stage (see
f) TV monitor
g) 20 MHz oscilloscope (optional)
Alteronics- Equipment available from Alteronics
(1-530-589-4926). Ask about their new combination sweep function generator
and controller box unit built for just this type of experimental research.
A great deal of very useful work can be done
at relatively low magnification (~400 power) when dealing with one cell
animals and multicell parasites. However, when trying to find the
lethal ultrasound frequencies for bacteria much higher power is needed
(1,200 to 2,500 power) and some special light staining technique such as
Rife used are very helpful and definitely needed for good research results
(finding the lethal ultrasound frequencies).
is the conceptual flow chart for carrying out the experimental research.
The intensity (energy / area / time ) of ultrasound output of the piezoelectric
transducer of Figure 7B is a very non-linear
function of the peak to peak voltage of the driving voltage signal.
The intensity increases to the fourth power of the peak to peak driving
voltage. For example, if the peak to peak voltage of a sine wave
driving voltage is doubled, the sine wave pressure wave output intensity
is increased by a factor of 16 = (2)(2)(2)(2).
It is only the sine and cosine voltage wave forms which are transformed
into cosine and sine wave pressure waves respectfully (see Figure
8). All other voltage wave forms are transformed by the piezoelectric
transducer into another type of wave form. For example, a voltage
triangle wave form is transformed into a pressure square wave form
by the piezoelectric transducer
(see Figures 9A and B).
All commercially available piezoelectric transducers
have an effective cut off frequency above which they can not produce
significant and generally useful ultrasound output. The best commonly
available PZT piezoelectric transducers that I use, begin to quickly lose
their ultrasound producing ability a little above 12 MHz. To get
around this shortcoming, there is a trick. That is, to use a voltage triangle
wave form at a frequency below the cut off frequency of the piezoelectric
material being used and use the hidden higher frequency ultrasound components
in the generated pressure square wave to kill the microorganisms.
Figure 9C, D, and E illustrate the first
three hidden Fourier components in the pressure square wave of Figure
9B which was generated by the transducer being supplied with the voltage
triangle wave form of Figure 9A.
10A and Figure10B show
the power absorption / power radiated verses frequency curves for some
mechanical resonators / oscillators. The curve of Figure 10B where
b=bo is a more realistic looking shape for real viruses, which are in general
the easiest structures to destroy due to their high symmetry. Everything
stated in the caption of Figure 10A still holds true, only it is more obvious
in Figure 10B.
Here are the technical details for implementing
the experimental setup shown in the flow diagram of Figure 7A, in order
to kill specific microbes.
Examples of scanning technique
1) The controller box going from 0 to +10 volts in time T and
connected to VCG input on a B & K sweep function generator set
to 10 MHz.
For our purposes, we need to know the relationship (the particular equation)
between frequency (F) and time (t) in the experimental run when the controller
box voltage starts at 0 volts and linearly progresses to +10 volts in time
T. Refer to Figure 11.
F = M t + B
F = First variable, M
= Slope of line, t = Second variable,
B = F axis intercept
(Rise / Run)
Run = t2 - t1, Rise = F2 - F1 ,
M = (F2 - F1) / (t2 - t1)
Figure 11, F1 = 10 MHz, F2 = 2 MHz, t1 = 0, t2 = T.
Using these values we obtain
M = (- 8 MHz / T). Substituting in initial values of frequency
and time ( 10 MHz and 0) into our straight line equation above we obtain:
F = ( - 8 MHz / T ) t + 10 MHz
What this last equation tells us is that once you place the total time
(T) for the scan into the equation you can find the frequency of the generator
at any specific time t. So using the time (t) readout on the video
camera / VCR you can determine the frequency at which the microbe disintegrated
2) Controller box voltage output going from +10 volts to
0 volts in time T. See Figure 12.
Using the same procedure as before we obtain:
F = ( + 8 MHz / T ) + 2 MHz
Suggested Lethal Ultrasound
Let us first deal with cancer. If cancer
is suspected, it is important not to kill off a tumor too quickly.
If large amounts of tumor are killed off, you now have a bacterial feeding
ground which can lead to toxemia which in turn can lead to kidney and liver
failure. So, if the suspected cancer you have is susceptible to specific
frequencies of ultrasound, as the great majority of cancers were in Dr.
Royal Raymond Rife's time, you should consider perhaps one treatment cycle
every two or three days giving the body adequate time to deal with the
kill off. However, if you live in California or some other "progressive"
state which prefers their citizens not to think too much for themselves,
you must ignore this entire last paragraph, despite my constitutional rights
of free expression.
Under California law (AB 1707.1) "The sale, offering for sale,
holding for sale, delivering, giving away, prescribing or administering
of any drug, medicine, compound or device to be used in the diagnosis,
treatment, alleviation or cure of cancer is unlawful unless (1) an application
with respect thereto has been approved under Section 505 of the Federal
Food, Drug and Cosmetic Act or..." .
In California, you are only allowed to treat cancer with 1) whole body
poisoning chemotherapy which heavily damages the immune system and is sometimes
carcinogenic in nature, 2) X-Ray radiation which is massively carcinogenic
in nature, and 3) disfiguring and disabling surgery.
Your health and well being in California are, for all practical purposes,
of very low priority to law makers. In my opinion, the law makers
are a combination of dupes and PAC whores of the vested pharmaceutical
/ AMA interests of the main stream allopathic establishment. Under
the guises of public health and safety, the allopathic medical establishment
have (under the law) effectively taken away much of your control over your
own body and the right to choose your own health / illness care treatment.
The average chemo and radiation "doctor" makes well over two hundred and
fifty thousand dollars a year for what in my opinion is essentially quackery.
The cancer industry in the U. S. is a two hundred billion dollar a year
business. It is time to take back what is rightfully ours by changing
the laws. Our state and ferderal legislative bodies need to do what
the Legislative Assembly of Alberta, Canada did in May 1996 when they got
fed up with their allopathic medical establishment. Here is the paragraph
they added to their law books.
" A registered practitioner shall not be
found guilty of unbecoming conduct or be found to be incapable or unfit
to practice medicine or osteopathy soley on the basis that the registered
practitioner employs a therapy that is non-traditional or departs from
the prevailing medical practices, unless it can be demonstrated that the
therapy has a safety risk for that patient unreasonably greater than the
Is this not a common sense, honest, and intelligent way to practice
medicine and give 'We the People' safe, effective medical treatment options?
Are your state legislative representatives capable of writing a bill that
would put this paragraph on our law books and give 'We the People' the
medical treatment options we need, but are currently denied to us by vested,
monopoly like interests? We need a bill that covers all licensed
health care professions.
Since, I am not a allopathic medical doctor, I can
not give you medical advice under the law in California and many other
states. So what follows is in no way to be considered medical advice.
It is only I, Gary Wade, excersizing my right of free verbal and written
expression under the Constitution of the United States of America.
As a practical matter, if you wish to experiment on yourself to see if
you can kill off a cancer tumor on yourself, you will need a piezoelectric
transducer, possibly a controller box, and a standard sweep function generator
used by electronic technicians. Get a sweep function generator that
has a four digit LED readout (a 10 MHz B & K unit will
do). There are over a dozen ultrasound equipment manufactures in
the US. The ultrasound transducers from any of these manufactures
However, the best and cheapest piezoelectric transducer available is
from Alteronics listed above. Also, Alteronics
has a cheap and reliable controller box available. There are several
experimental treatment protocols you can try. First, you can simply
slowly scan through the full frequency range of the sweep function generator
while on the triangle wave setting, using the controller box. The
function generator is set to maximum output voltage and is always of a
positive polarity. Secondly, you can slowly scan through and around
either 11,780,000 or 23,560,000 cycles per second ( one or both of
these frequencies were used by Rife to kill the BX cancer virus).
This is achieved by using hidden Fourier components of 11,780,000
or 23,560,000 cycles per second. For example, looking at the equation
associated with the pressure square wave in Figure 9, we see the second
hidden Fourier frequency component has a frequency of 11,780,000 cycles
per second, if the triangle voltage wave frequency coming from the function
(11,780,000 cycles per second) / 3 = 3,926,666 cycles per second.
Similarly, the second hidden Fourier component is 23,560,000 cycles
per second, if the triangle voltage wave form has a frequency of
7,853,333 cycles per second. So, by slowly scanning through these
lower triangle voltage wave form frequencies, the hidden Fourier higher
frequency pressure sine waves are generated.
The third experimental protocol is perhaps
the most interesting. It has been found empirically by several independent
researchers that a pressure square wave of 2127 cycles per second can quickly
destroy many types of cancer tumors. However, as stated earlier,
you do not want to kill off a tumor to quickly. A conservative treatment
approach that has achieved successful results is as follows: Running
the function generator at maximum output, place the transducer on or near
the tumor for one minute. Then wait three days to see if the kill
off was O.K. or too big ( very painful inflammation of tumor tissue).
If O.K. continue treatment . If, not then wait until all this subsides
before treating yourself again. When treating yourself again use
one half the treatment time used before. Again, wait a couple of
days to see how big the kill off was.
It is best to kill off the cancer in small amounts over two or three
months. This will allow the liver and kidneys to do their jobs without
making the body toxic. Large amounts ( 5 to 10 grams) of vitamin
C can be taken daily with lots of water (minimum of 10 oz. per gram of
vitamin C) to detox. A buffered vitamin C is probably best for most
people. However, do not use a buffered vitamin C with calcium in
it. This form of vitamin C seems to promote cancer growth.
The actual mechanism that kills the cancer
cell when using the 2127 cycles per second pressure square wave is not
known. However, my quess is that one or more of the Fourier pressure
wave components hidden in the 2127 cycle pressure square wave closely matches
the mechanical resonance frequency of one or more of the cell's specific
ion gates. Cancer cells have very abnormal ion concentrations in
them. If ion gates for specific ions are opened up by these Fourier
components the ion concentrations can be changed drastically inside the
cancer cell and the bi-lipid membrane potential difference can fall drastically.
If this potential difference fall is too large the cell can not recover
Documents 1 and 2 are photo copies of actual
Rife research note book pages. A set of approximately twenty
24 such pages were supplied to me by Jasson Ringas. Table 1 is a
compilation of the key frequency data for the microbes listed in those
In table 2 are listed some of the standard
disease treatment frequencies used by voltage square wave generators, such
as those made by John Crane. When electrodes are used on the body,
which have voltage square waves applied to them, these voltage square waves
among other things produce discontinuous steady state ion transport in
the body electrolytic fluids. This discontinuous steady state ion
transport produces sets of pressure square waves that have the full spectrum
of relative phase differences, but all centered about the same frequency.
These pressure square waves have the same center frequency as the driving
/ applied voltage square wave. And just as indicated in Figure 9
there are many hidden Fourier higher frequency components in the pressure
square wave. Using voltage square waves to produce pressure square
waves in body fluids is very inefficient. However, by using a voltage
triangle wave put into a piezoelectric transducer, much more powerful pressure
square waves can be produced. Therefore, using voltage triangle waves
of the same frequency as listed in Table 2, we can expect much quicker
and dramatic results. By using the formula given with Figure 9, you
can use a standard sweep function generator and using the sine wave output
function to see which hidden Fourier frequency(ies) are actually responsible
for the dramatic results often seen.
Gary Wade can be contacted at the American Institute of Rehabilitation.
All information posted on this web site is
the opinion of the author and is provided for educational purposes only.
It is not to be construed as medical advice. Only a licensed medical doctor
can legally offer medical advice in the United States. Consult the healer
of your choice for medical care and advice.