( Originally published in Health Freedom News, August
/ September 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 a 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
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
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 shown 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,B,C,D 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 6A,
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 (OH-) and
a hydronium ion (H+) . Both the hydroxyl and the hydronium ion in water
will attempt to execute the motion illustrated in Figure
5 , if exposed to the crossed electric and magnetic fields. However,
the hydronium ion will execute the motion at a much higher rate (frequency)
then the hydroxyl ion because of it's much smaller mass (*)
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
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
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
ENTER CHARGE DENSITY WAVES
Besides the broad band ultrasound generation, there
are other phenomenon 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 6A &
Figure 6 B,C ). 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 end 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
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 a 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.
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
THE TECHNICAL CORNER
The frequency of oscillation of charged particles
in a crossed electric and magnetic field is given by:
F = (Q)(B) / (2 * )(M) ;
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) ;
where E is the electric field strength in volts per meter, Q is the magnetude
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.
Fr = ------------------
2 ( LC2 )1/2
The out put frequency of 555 chip circuit of Figure 7 is Ft.
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 frequeny 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 varring the pot
value while whatching the voltage amplitude accross the coil with an oscillascope,
the circuit can be tuned to resonance ( maximum voltage amplitude across coil
1) Health Freedom News, August 1994, Pg. 36.
2) Health Freedom News, November / December 1994, Pg. 24.
3) Lancet, July 26, 1986, Pg. 229.
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.