MAGNETIC PULSE THERAPY AND RIFE HEALING
“EXCITING POSSIBILITIES IN PULSED, INTENSE,
MAGNETIC FIELD THERAPY: A PHYSICIST'S VIEW”
BY GARY WADE
(Originally
published in Health Freedom News 1998)
Imagine
devices that can disable and destroy microorganisms-viruses, bacteria and fungi
- by means of a pulsed, intense, magnetic field!
They are not devices for the distant future. They
are for today! Already several different pulsed magnetic field instruments are
being used in the alternative health field.
Many claims and suggestions are being made for and
about them. Let's look into their validity. Let's also look at a simple device
that uses a strong permanent magnet and an oscillating magnetic field generated
by a coil of wire. And, in addition, let's consider what broad band ultrasound
* directed inside animal and human tissue can do and how it can destroy
microorganisms.
During the 1920's and 30's, Dr. Royal Raymond Rife
discovered that every microorganism has at least one frequency of ultrasound
that at ultra-low intensity, can easily disable and/or destroy it. Strange as
this may seem, it is easy to understand when you learn more about the
substructures of microorganisms.
All microorganisms apparently have protein clump
structures, which are periodically spaced and elastically coupled. They are
capable of supporting resonant, standing, mechanical waves. Roughly half of the
viruses that attack humans are lipid coated. Let's consider the outer structure
(capsid coat ) of the common lipid-coated viruses that attack human beings. Figures 1A and B illustrate their geometrical
construction features. The structure in Figure 1B is called an icosahedral. As show in Figure
1A, it is composed of twenty identical equilateral triangles. Figure 2A and B illustrate two specific examples of virus
capsid coats. The dark disks in Figures 2A and B represent individual single
protein molecule spheroids. These spheroidal protein molecules are weakly
bonded to each other. This spheroidal protein structure is elastic. If the
protein capsid coats illustrated in Figure 2A and B are folded up to form the
completed virus capsid coat illustrated in Figure 1B, a structure will have
been formed that has periodically spaced, elastically coupled, protein clumps
that close back on themselves. As previously stated these closed on themselves
periodically spaced protein structures can support resonant standing mechanical
waves. Figure
3 shows several examples of these
periodically spaced closed structures found on the capsid coats formed from the
examples of Figures 2A and B. The bond between these adjacent protein molecules
are relatively weak. This means that if the amplitude (displacement from rest
position) of the protein molecules becomes too large during mechanical
oscillation, the physical / chemical bonds between the adjacent molecules will
rupture and this essential microbe structure is destroyed.
An ultrasound generator can supply the mechanical
oscillations. Figure 4A shows the periodically spaced closed
structure of Figure 3A laid out linearly for ease of graphic display. Figure 4B,C,and D illustrate some of the standing mechanical
wave oscillation modes that the periodically spaced closed structure of Figure
3A can support. The standing wave mode illustrated in Figure 4B where the
adjacent protein clumps oscillate 180 degrees out of phase is the most
stressful oscillation mode. When adjacent protein clumps oscillate 180 degrees
out of phase, one protein clump is moving upward while its adjacent clumps are
moving downward and visa versa. At maximum displacement of the protein clump
from their equilibrium position, the stress at where the adjacent protein
clumps are joined become a maximum. If the stress becomes large enough the
bonding between adjacent protein clumps breaks down and the essential or
critical structure for holding and delivering the virus genetic material is
critically damaged or destroyed. This means the virus can not infect a new
cell. Also, viruses that are forming and budding off of infected cells can be
destroyed by this same method. This destruction / disintegration of forming and
budding off viruses leaves holes in the infected cell's membrane, which can be
fatal to the infected cell, which is actively producing viruses.
ENTER THE PULSED MAGNETIC FIELD
At this point you may well be wondering how intense
pulsed magnetic fields can produce the mechanical oscillations at ultrasound frequencies
needed to destroy virus capsid coats as well as other periodically spaced,
elastically coupled, and closed on themselves critical structures in
microorganisms in general. Consider Figure 5, which illustrates the type of motion a
charged particle executes when it is placed in a crossed electric and magnetic
field. In Figure 5 the magnetic field is at right angles to the plane of the
page (perpendicular) and the electric field is in the plane of the page. If the
charged particle released from rest in such a crossed magnetic and electric
field is a proton embedded in water, then as the proton attempts to execute the
motion depicted in Figure 6, it must collide with / move about adjacent
water molecules. It does this moving about of adjacent water molecules in a
periodic fashion as depicted in Figure 6. This periodic moving back and forth
of water molecules is the generation of ultrasound. Regular water at room
temperature has approximately one in a million water molecules at any instant
in time disassociated into a hydroxyl ion (
For our more technically trained readers, I have
written the equations that describe the frequency of ultrasound generated by
the ions oscillating in the crossed electric and magnetic field, along with the
amplitude of oscillation in a separate technical section at the end of the
article.
Question: How do you get this crossed electric and
magnetic field in water?
Answer: You expose the water to a changing magnetic
field strength. It is known from experiment and theory, that when a magnetic
field at some location is changing in strength, an electric field is created
with it's direction at right angles to the direction of the existing magnetic
field at that location. In other words a crossed magnetic and electric field as
illustrated in Figure 5.
The frequency of mechanical oscillation is directly
proportional to the magnetic field strength. For example, if you increase the
magnetic field strength by a factor of ten, then the frequency of ultrasound
generated by the ion oscillation increases by a factor of ten. The amplitude
(displacement) of oscillation is directly proportional to the electric field
strength. The electric field strength is determined by how fast the magnetic
field strength is changing. It is directly proportional to the instantaneous
rate of change of the magnetic field strength. So, to have both higher
frequencies of ultrasound generated and for these frequencies to have high
intensity / amplitude, the magnetic field at the location of interest must be
both very strong and be changing it's strength at a high rate. Hence, what is
required is a high intensity pulsed magnetic field. This is achieved by rapidly
discharging a high voltage capacitor through an appropriately designed wire
coil. If such a coil is placed on the surface of a person, when it has a high
voltage capacitor discharge through it, it produces a continuum of magnetic
field strength throughout the body and therefore a continuum of oscillation
frequencies throughout the body along with a continuum of associated
oscillation amplitudes. The highest ultrasound frequencies with also the
highest displacement amplitudes will be generated by hydronium ions directly
under where the coil is placed. The lowest frequencies and lowest amplitudes of
oscillation will be at body locations farthest from the coil. Each time the
high voltage capacitor is discharged through the coil, the electric current
oscillates back and forth between the coil and the capacitor for approximately
ten oscillations for most capacitor and coil combinations of interest. Each
oscillation cycle being a little weaker than the pervious one. During each of
these ring down oscillations a crossed electric and magnetic field is generated
in animal tissue with the concurrent generation of broad band ultrasound, which
can destroy the critical periodically spaced closed on themselves protein
structures of microbes.
ENTER CHARGE DENSITY WAVES
Besides the broad band ultrasound generation, there
are other phenomena occurring which can disable microbes. The transient
electric field associated with the pulsed / oscillating magnetic field
generates charge density waves in your body's electrolytic fluids (salt
solutions). These charge density waves are traveling compressions and rareifications
of the normal salt solution ion concentrations. For example, when the transient
electric field produced by the pulsed magnetic field is at some angle into or
out of the animal's skin, the ions in the body fluids just under the dead skin
layer will momentarily separate themselves into a dipole charge layer in such a
way as to minimize the transient electric field at that location. That is the
positive ions such as potassium, sodium, magnesium, calcium, etc. and the
negatively charged ions such as chlorine, hydroxyl ion, etc. separate
themselves into two opposing layers of higher than normal concentration of each
ion in one of the layers and low than normal concentration in the other layer.
During the dipole charge layer formation process, which is being driven by the
transient electric field, some ion types are being drawn in toward the dead
skin layer while others are being forced away from the dead skin layer.
This is a dynamic process, when those ions are
pulled toward the dead skin layer, they leave behind a vacancy in their
concentration which is filled in by adjacent ions of their own kind and in turn
these ions leave a vacancy which is filled in by adjacent ions of their own
kind. In this way a rareification wave of ion density is propagated away from
the dipole layer generation region and into the body interior. Similarly, when
a ion type is forced away from the dead skin layer by the transient electric
field, a compression (higher than normal concentration) of that ion is formed
and this compression wave is also propagated into the body interior. Since
these charge density waves are effectively traveling excesses of either
positive or negative charge, they have traveling electric fields associated
with them. These traveling electric fields can when strong enough denature /
rearrange essential delicate protein structures on virus and bacterial
surfaces. One good example of this sort a activity, is the denaturing of the
proteins of snake venom by charge density waves generated from shocking the snake
bite region with high voltage discharges from the spark coil of a car. Another
example, the HIV virus has a glycoprotein molecule known as gp-120 displayed on
it's surface. This protein is designed to match up and attach to a very
specific protein CD4 on the target cell membrane. If the very specific shape,
size, and charge configuration of the gp-120 is rearranged / changed by the
transient electric field from the charge density wave, then gp-120 can not
attach to CD4 and the virus can not infect the target cells. The virus is
effectively destroyed. This displaying on the virus surface of a specific
protein with a specific size, shape, and charge configuration to attach to a
specific protein on the target cell is a standard virus attribute and therefore
provides for a simple method to deactivate viruses.
It should also be pointed out that the electric
fields from the net charge of the charge density waves causes adjacent cell
membranes to move to and fro as the charge density waves pass between them and or
around them (see Figure 6). This is do to the fact that body cells
maintain a dipole charge layer across their bi-lipid cell membranes. The
electric field of the charge density wave reacts with the charges of the cell's
dipole charge layer to make the cell membrane act like a sound speaker
diaphragm. However, here we are dealing with diaphragm oscillation rates in the
million cycles per second range (ultrasound). This form of broad band ultrasound
generation can also destroy microorganisms.
Now that we have a some understanding of how a
crossed electric and magnetic field and charge density waves can be used to
generate broad band ultrasound in body fluids (saline solutions), consider the
circuit schematic of Figure 7 (see THE TECHNICAL CORNER at in of article).
In Figure 7 we have a 555 timing chip oscillator driving a simple LC tank
circuit that has a small very strong permanent magnet at the coil center. The
555 oscillator is tuned to match the resonance frequency of the LC tank circuit
(see technical section for details). The tank coil oscillations provide the
rapidly changing magnetic field strength to produce the electric field at right
angle to the magnetic field of the permanent magnet. We can therefore expect
the generation of broad band ultrasound, which can destroy microorganisms. The
maximum frequency of ultrasound generated by this device is determined by the
magnetic field strength at the pole face of the permanent magnet. As a rule of
thumb it is approximately one million cycles per second per one thousand gauss.
Neodymium magnets of ten thousand gauss are commonly available, so with such a
magnet we can expect to have approximately ten mega hertz as our maximum
ultrasound frequency generated. A large percentage of microbes can be expected
to have one of their lethal ultrasound frequency at or below ten mega hertz.
So, what we have here is a simple cheap way to possibly treat many microbial
problems.
You technoid readers with a more apocalyptic bend of
mind, will note that the device of Figure 7 can be scaled up in size to treat
the entire human body all at once. For example, consider Figure 8 where we have a auto junk yard electromagnet
with a coil securely mounted on it. This coil can be powered by a standard 60
cycle wall current or preferably by a high power audio speaker amplifier
running at several thousand cycles per second. The potential need for such an
industrial size whole body treatment unit is the danger of possible coming
plagues. As Dr. Len Horowitz has so clearly documented in his book, AIDS and
Ebola; Nature, Accident or Intentional?, government research scientists around
the world have both accidentally and purposely created very deadly viruses and
bacteria. Some of these scientists and governments have also purposely released
some of these deadly viruses and bacteria to selected populations, i.e.
"special vaccine batches". A community operated de-plaguing center
can be set up in any community that has an auto junk yard electromagnet or its
equivalent. We are dealing here with the scum of the earth and we can put
nothing pass them. Not even reducing the world population down to 500 million
over the next 50 years using deadly plagues, some of which maybe very geno-type
specific. They have a Nazi mentality, which needs to be housed permanently in a
federal prison.
CONCLUSION
When properly used pulsed magnetic fields can
produce broad band ultrasound which can, as Royal Raymond Rife showed in the
1920's and 30's, destroys microorganisms which can maintain a disease state in
the body.
The next time you hear a spokesperson / authority
figure for the allopathic medical establishment bad mouthing and pooh-poohing
alternative health energy medicine, please send them a copy of this article and
suggest to them that they should go back to school and take some physics, for
energy medicine is the medicine of the future and is becoming available now.
(See links below for less technical articles)
THE
TECHNICAL CORNER
The frequency of
oscillation of charged particles in a crossed electric and magnetic field is
given by:
F = (Q)(B) / ( 2P )(M) ; Equation 1
where Q is the
charge in coulombs on the particle, M is the particle mass in kilograms, and B
is the magnetic field intensity in webers per meter squared at the particle
location.
The amplitude of
displacement (S) of the ultrasound waves given by Equation 1 is approximately:
S = (2ME) / (QB2) ; Equation 2
where E is the
electric field strength in volts per meter, Q is the magnitude of the charge on
a particle in coulombs, and M and B are as before.
555 CHIP SQUARE
WAVE OSCILLATOR CIRCUIT
The resonance
frequency of the tank circuit (see Figure 7) formed by L and C2 is Fr.
1
Fr = ------------------
2 ( LC2 )1/2
The out put
frequency of 555-chip circuit of Figure 7 is Ft.
1.44
Ft = -------------------
2R1C1
For the circuit to
be at maximum out put power for maximum ultrasound generation in the tissue Fr
= Ft. Choose a C2 and L combination that gives a Fr that is in the upper
frequency range of the 555 chip's operating range, i.e. 105 sec.-1 . Now choose a R1 and C1
combination that makes Ft = Fr. Resistor R1 can be a composite resistance made
up of a resistor pot and resistor in series. By varying the pot value while
whetting the voltage amplitude across the coil with an oscilloscope, the
circuit can be tuned to resonance ( maximum voltage amplitude across coil).
* Broad band
ultrasound - A continuum of ultrasound frequencies covering a large range of
ultrasound frequencies. Ultrasound is generally considered to be any frequency
of sound (mechanical vibration) above twenty thousand oscillations per second.
References:
1) Health Freedom
News, August 1994, Pg. 36.
2) Health Freedom
News, November / December 1994, Pg. 24.
3) Lancet,
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