SYNERGISTIC ENERGY MEDICINE THERAPUTICS
FOR USE BY ALTERNATIVE HEALTH PRACTITIONERS
by Gary Wade, Physicist (5/15/07)
OBJECTIVE
- To present in some
technical detail several experimental energy based treatment modalities that
can be used simultaneously or sequentially to produce a synergistic therapeutic
outcome that in general greatly exceeds results coming from any one of these
treatment modalities used separately.
Furthermore, the medical practitioner and or any other reader of this
material should appreciate that this information should be common knowledge to
all medical practitioners and be put into practice regularly. It is hoped that
each practitioner will be creative with this presented information and
incorporate as much as possible various forms of the technologies and treatment
modalities discussed and illustrated below.
Specific objectives/goals will vary
somewhat from patient to patient.
However, in general, as a minimum, two goals will be sought during each
patient treatment
session: 1) Greatly accelerated
adenosine triphosphate (ATP) production, and 2) Killing off of both localized and systemic microbial infections.
ATP is the essential cell work
molecule. The energy obtained from
consuming food in the cellular respiration is stored in the ATP molecule. ATP production in adequate amounts is
essential for cell life, cell maintenance, cell repair, and maintenance of a
strong immune system. This implies that
ATP is essential for tissue repair in general.
The removal of microbial infections in the body tissue is essential for
maximum tissue repair and regeneration and good health in general. As examples of needed ATP production and
needed microbial kill off for tissue repair and regeneration we will consider
the situation surrounding strokes, Multiple Sclerosis (MS), and autistic
children. However, the principles and
technologies that will be considered can be applied to most tissue repair
needs/conditions and microbial driven health problems in general.
It has been empirically shown that both
hyperbaric oxygen treatments and high intensity static magnetic field
treatments are effective in returning stroke victims to near normal
condition(ref.1,2). In the case of
hyperbaric oxygen treatment, as the air pressure approaches 3 earth atmospheres
absolute a significant amount of oxygen dissolves directly into the blood
plasma of the lungs and is carried out to the body tissue without the need for
red blood cells. Each time in the treatment
cycle when the pressure is reduced back to normal atmospheric pressure, the
cells in the poorly vascularized brain injury area are again starved of oxygen
and produce hormone-like substances which initiate arterioles, veinlets, and
capillary growth into the damaged region(s).
Usually after 30 to 50 such hyperbaric oxygen cycles, the stroke region
is fully re-vascularized. Similarly,
after approximately 50 to 100 hours of intense magnetic field therapy (5,000 or
more gauss) the stroke region is also re-vascularized. What these two different treatment
modalities have in common is that they greatly increase the ability of the
affected (oxygen deprived) cells in and around the damaged region to produce
ATP. ATP is the cell fuel, which is
necessary for most cellular energetic activity. ATP powers the cell and all tissue repair and maintenance.
In the case of hyperbaric oxygen
treatment, the cellular ATP production is increased due to the added
availability of the needed oxygen for ATP production, the oxygen in the case of
stroke being one of the important limiting resources for needed ATP
production. However, in the case of
intense static magnetic field therapy, the applied magnetic field can
apparently greatly accelerate the enzyme reaction rates of key enzymes in the
respiratory chain inside the cell organelle the mitochondrion and thereby
increases ATP production. The applied
magnetic field generally often increases enzyme reaction rates (ref. 3). In other words the cell more effectively
uses all available oxygen and has a more efficient cellular metabolism. The removal of the applied magnetic field
may also trigger a hormone release from oxygen deprived cells to produce
re-vascularization into the region.
Approximately 85% of the time, a stroke
is caused by a small clot going to the brain and lodging in a small artery and
thereby stopping down stream blood flow.
The other 15% of the time a small to large artery blows out (ruptures)
causing a hematoma. This is usually
caused by high blood pressure. The
stroke causing blood clots are often apparently formed in association with high
blood pressure and it’s associated turbulent blood flow at the location of an
artery restriction region, where there is a plaque build up. Research has shown using catheter
temperature probes that these large plaque regions often have a temperature of
101 degrees F to 104 degrees F, indicating an active infection in the artery
wall (ref. 4). Biopsy of these artery
wall regions, usually show, bacterial and or fungal infections. Such an infection will have inflammation or
swelling associated with it that significantly adds to the restriction of
arterial blood flow. Also, the
infecting nano- bacteria usually have a calcium rich outer cell walls which are
actively involved in the formation and maintenance of the arterial plaque. The tissue of organs down stream from this
combination inflammation and plaque induced restriction can experience
significantly lower blood flow and therefore less oxygen supply. These oxygen deprived organs or tissues will
release hormone like compounds which have the end result of increasing blood
pressure until adequate blood flow through the various artery restriction
regions are achieved. By using the
right ultrasound frequencies to kill off the bacteria and fungus infections in
the artery wall, the inflammation can be removed and therefore significant
amounts of the restriction and associated higher blood pressure are
removed. This anti-microbial ultrasound
technology is Rife type technology, which will be discussed below.
The other main driver of high blood
pressure is dehydration. Being
dehydrated requires the human body to use a lower blood volume. This in turn requires the artery wall
muscles to contract so that the arteries have a narrower cross section. The
narrower artery cross sections require the heart to pump harder and faster to
get an adequate blood flow supply to all body organs and tissue. The majority of the middle aged and older
adult population are generally dehydrated to varying degrees. This problem is compounded by half the
country’s drinking water supply being fluoridated by 1 ppm or more and
therefore poisonous to most all biological chemical activities. If we had legislators which were technically
educated in chemistry, biology, and physics instead of the law (lawyers) we
would not have fluoridated water and all of its associated health problems (
brittle bones, premature aging, lower fertility, lowered immune system functioning, high cancer rate, much more
docile behavior (this is why both the Nazis and Soviets fluoridated the water
in their concentration camps), etc.)
All patients should be checked for dehydration and be encouraged to
drink approximately one gallon a day of good non fluoridated water, and to
avoid fluoridated water like the poison it is.
Multiple Sclerosis
In the case of MS it has been shown that
hyperbaric oxygen therapy as well as intense static magnetic field therapy can
be very therapeutic in at least partially reversing the condition (ref. 5). We may assume as one reasonable hypothesis
that the increase in oxygen from hyperbaric oxygen treatment facilitates ATP
production and tissue repair. However,
some MS seems to be associated with on going microbial infection in the neural
tissue. It may be an anaerobic microbe,
which is susceptible to damage and death from increased oxygen to the
tissue. Also, these patients are good
candidates for low intensity broad band ultrasound treatment to help in
cleaning out all forms of microbial infection.
It was discovered in the 1920’s and 30’s by Dr. Royal Raymond Rife that
every microbe (virus, bacteria, fungus, etc. ) he studied had at least one
ultrasound frequency that destroyed it very easily. By very slowly scanning through the entire range of ultrasound
frequencies used by Rife and then some, it is possible to kill off the great
majority of microbes. This is what low
intensity broad band ultrasound units, such as the Ultra 10A, are all about. To get a good overview of Rife type
technologies, please read the article VIBRATORY ENERGY MEDICINE .
Autistic Children
In the case of autistic children, they
can be separated into two groups. One
group in which the children were born with abnormal brain structure and or
abnormal neural physiology. The second
group developed autistic behavior shortly after receiving one or more
vaccinations; i.e. MMR shots. This is now by far the dominate cause of
autism. With the continuous on going
increase in the number of mandatory vaccines for children the autism rate has
gone from approximately 1 in 5,600 to 1 in 160. Put simply, it is the vaccines stupid. This second group may therefore also be suffering from a vaccine
additive (toxin) and or an on going microbial infection in brain and or other
body tissue, which came from the
vaccine(s). It is not necessary for
neural tissue to be virus or microbe infected for the neurological
malfunctioning of autism to occur. It
is only necessary for toxins generated by the infection to be able to cross the
blood brain barrier or to disrupt the biochemistry of a key body organ such as
the liver. For example, the drug LSD
does not act directly on the brain, instead it inhibits the production of two
enzymes in the liver that are normally secreted into the blood and taken to the
brain. They are therefore also good
potential candidates for experimental low intensity broad band ultrasound
treatments from Rife type technology, such as the Ultra 10A unit.
It is believed that general tissue
oxygenation and significantly greater ATP production will be very helpful in
the improvement and recovery of all of the above discussed conditions. However, there is a need to go after possible
microbe infections (viral, bacterial, and ?) in the patients for whom the
infection may be driving their condition and stopping or greatly slowing their
recovery (tissue repair). And this will
also hold true for many other types of conditions that a alternative health
practitioner may encounter. Five energy
based methods for potentially achieving this goal of microbial cleansing are:
1) Low intensity broad band ultrasound
treatment, 2) Ozone decay light
therapy, along with infra red LED light
therapy , 3) High intensity “color”
therapy, 4) Charge density wave therapy, and 5) Pulsed magnetic field
therapy. These five methods will be
discussed in more detail below, but first we will concentrate on ATP production
enhancement.
OVERVIEW
OF PROPOSED TREATMENT MODALITIES FOR ENHANCED ATP PRODUCTION
Specifically, the proposal to achieve
greatly enhanced ATP production is to combine simultaneously the exposure of
the patient to ozone decay light / infrared LED light, a much larger than
ambient magnetic field, and a very high concentration of negatively charged
oxygen molecules. The function of each
of these modalities and how they interact in a way to give greatly enhanced ATP
production will be discussed below.
Negative Oxygen Molecule Ion - A negatively charged oxygen molecule is a
oxygen molecule with an extra negatively charged electron. The negatively charged oxygen molecule seems
to have at least three uses/functions in our body: 1) To help in the
transport of other oxygen molecules from the surface of red corpuscles in the
capillaries to the outside of the tissue cell bi-lipid membrane, 2) To help in transport of oxygen molecules
across the cell bi-lipid membrane into the cell, 3) To donate a spare electron when needed to be used in the series
of enzyme reactions of the respiratory chain of the cell’s mitochondria, which produce the great majority of the cell
fuel ATP.
1) Transport
of Oxygen Molecules in Interstitial Cellular Fluids- When red blood corpuscles enter the capillaries, they deform from
a plate/disk shaped geometry into a cone shaped shell, as shown in cross
sectional view in Figure 1. These deformed corpuscles form or obtain a
negative charge on their leading edge cone surface (ref. 6). It will be postulated that either one or
both negative oxygen molecules are created at or are attached to the surface of
the red corpuscles. ( Perhaps the
acupuncture meridian system is supplying some of these negative oxygen ions to
the red corpuscle surface. We will come
back to this possibility later on. )
And furthermore, as the red corpuscle transits the capillary, oxygen
molecules being released by the hemoglobin inside them interact at the
corpuscle surface with the surface negatively charged oxygen molecules to form
higher order negatively charged oxygen molecule clusters N(O2)-,
where N is a small integer. These
oxygen molecule clusters are maintained by the exchange forces from
sharing/fighting over the extra electron.
These clusters are only semi stable and will “dissolve” as they transit
the interstitial spaces between the cells.
These negatively charged oxygen molecule clusters move into the
interstitial spaces between cells.
These oxygen molecule clusters are being moved along into the tissue by
diffusion processes, pressure differential, and a weak electric field. This weak electric field is setup in the
body tissue by electric currents supplied to the tissue by the Schwann cells
surrounding motor nerve axons and dendrites of skin sensor nerves (ref. 7).
2) Transport
of Oxygen Molecules Across the Cell Bi-lipid Membrane- It has been determined that oxygen molecules
are transported across the cellular bi-lipid membrane by/with the calcium ion
(Ca ++) (ref. 8, 9). I am not talking
about oxygen going along with the calcium ion through calcium ion channels or
gates in the cell membrane. I am
talking about oxygen molecules actively coupling with calcium ions and
diffusing or being actively transported across the cell bi-lipid membrane. The N(O2)- cluster will have a natural affinity for the
Ca++ ion and water molecular cluster
because they are opposite in charge and will attract each other. On the average approximately one N(O2)-
cluster should be closely associated or over lapping with the Calcium ion
molecular water cluster. Furthermore,
it has been determined that the phosphorous oxygen bonds (two electron pairs)
in the phosphate group of the head of the phospholipid molecule of the cell
bi-lipid layer ( see Figure 2 ) must be raised to an
excited state for the Ca++ ion to be
efficiently and actively transported across the cell bi-lipid membrane into the
cell and carry/drag the oxygen molecules with it (ref. 8, 9). Light in the top end of the infra red
light frequency range such as emitted
from meta-stable oxygen molecule decay is effective in raising the
phosphorous-oxygen bonds to the excited states needed to facilitate the active
transport of the combination calcium-oxygen charged cluster across the cell
bi-lipid membrane. This meta-stable
oxygen molecule decay light is also called ozone decay light which will be
discussed below.
3) Electrons
for Respiratory Chain - When looking at
the respiratory chain for ATP production it will be noted that for conversion
of this food stuff into carbon dioxide, water, and ATP there is a set of enzyme
reactions that pass along two electrons to be used in a catalytic fashion for
ATP production (Figure 3). (Consult a biology text book for all the
details on ATP production in the respiratory chain.) According to the respiratory chain enzyme reaction equations
there is no need for extra electrons from an outside source to be supplied to
the series of enzyme reactions. This is
an error. In the real world crap
happens, i.e. a transport electron in the respiratory chain gets lost somehow. The production of ATP comes to a halt until another electron is
found. Question, where can the enzyme
find a spare electron? Answer, a
negatively charged oxygen molecule waiting to under go a reduction reaction to
make ATP can supply the needed electron.
This ready availability of spare electrons keeps the ATP production at
an optimal production rate. To illustrate
this important phenomenon along with increased oxygen transport by negative
oxygen molecule ions, consider the experiment carried out by D.A.
Lapitsky. Lapitsky placed small animals
in a chamber with air of an abnormally low oxygen level. As the animals passed out and were about to
die from asphyxiation, he turned on negative ion generators in the chamber,
which generated negatively charged oxygen molecule ions. The animals became conscious, sat up,
sniffed the air, and began to run around the chamber. When the negative ion generators were again turned off the
animals soon passed out again (ref. 10, p. 52). I highly recommend that you read the book THE ION EFFECT by Fred
Soyka with Alan Edmonds ( ISBN #
0-553-20755-5 ).
Ozone Decay Light Therapy
and Infra Red LED Light Therapy- As
already stated above the infra red light emissions from meta-stable oxygen
molecules generated in the ozone decay process (see Figure 4) can raise the molecular bonds between the oxygen
atom and the phosphorous atom in the phosphate group on the phospholipid
molecules of the bi-lipid membrane to an excited state (see Figure 2). In this
excited state there is a rearrangement of charge configuration in the
phospholipid head of the lipid molecule in the cell membrane. This excited state with its associated
charge redistribution is required to cause efficient active transport of the
calcium ion and associated oxygen molecule(s) and or negatively charged oxygen
ion cluster across the cell bi-lipid membrane.
The human body is fairly translucent to this meta-stable oxygen molecule
decay light; specifically, the infra
red wave length 762 nm emitted by the 8 second half life meta stable Sigma
state going to the oxygen molecule ground state. This decay light can go into the body tissue and activate the
phospholipid molecule phosphorus and oxygen double bonds into an excited
relatively long half life state. It is
known from experiments that the rate of calcium ion transport (T) across the
cell membrane, which “drags” the oxygen ion complex with it, follows a high
power law of the intensity (I) of the infra red light in the frequency range of
that emitted from meta-stable oxygen molecule decay to the ground state (ref. 8, 9). In other words, T is approximately proportional to I to the Nth power, where N is a small
integer. For example, imagine that the
calcium ion /oxygen molecule transport rate across the cell membrane followed a
fourth power law of the infra red light intensity. This would mean that a doubling of the light intensity would
cause a 24 = 16 fold increase in transport. If the transport rate followed a sixth power
law of the light intensity, then with a doubling of the intensity there would
be a 26 = 64 fold increase in the transport rate across the cell
membrane. Of course this assumes that
there is that much calcium ion and oxygen available for transport across the
cell membrane. (This type of calcium ion transport is not to be confused with
calcium ion transport through specific calcium ion channels in the cell
membrane). The apparent reason for the
high power law of infra red light intensity has to do with the need to have two
or probably more adjacent phospholipid molecule heads in an excited state for
active transport of the calcium and oxygen molecule complex to be
efficiently actively transported across
the cell bi-lipid membrane. Therefore a
small increase in the intensity of the meta-stable decay light or some other
light in this wavelength region, for example light from a IR diode laser or
IR LED, generates a much larger
transport of the calcium ion and associated oxygen molecule ion clusters into
the cell. More oxygen is available for
ATP production and also negative oxygen molecules to keep the respiratory chain
moving efficiently.
As stated above the human body is fairly
translucent to this meta-stable oxygen molecule decay light. Upon absorption of this decay light by an
oxygen molecule inside the body, this oxygen molecule will go into a
meta-stable state. It can decay back to
normal oxygen emitting infra red light or it can chemically react or it can
pass its excitation energy onto another molecule. This meta-stable oxygen is very effective at damaging and
destroying many kinds of microorganisms and viruses. This is because meta-stable oxygen molecules are exceedingly more
chemically reactive than normal oxygen molecules. Anaerobic microbes are particularly susceptible to damage from
meta-stable oxygen molecules. This
could be particularly important in helping to clean out certain possible
infections in young children from vaccinations, which are driving their health
problems. This ozone decay light
applied along with experimental broad band low intensity ultrasound technology
can be expected to be a very powerful tool for cleaning microbe infections out
of the body.
While this meta-stable oxygen molecule
can/could be expected to be also harmful/damaging to normal cell chemistry,
this damage can be greatly mitigated by ample intake of anti-oxidant such as
vitamins A, E, and the mineral selenium and co-enzyme Q-10, etc.. Vitamin C should only be used after ozone
decay light therapy do to vitamin C’s strong chemical reaction with meta-stable
oxygen in the blood where it forms a toxic compound.
I first became aware of the potential
microbial transforming, debilitating
and killing power of ozone decay light when I read the unpublished work of my
friend Merlin Wolf. Many years ago
(~1969) he performed, for his company, a simple experiment in which he exposed
fungus cultures to ozone decay light.
He placed a group of fungus cultures contained in dishes with the glass
lids hermetically sealed on, into an air tight box which contained a high
concentration of circulating ozone gas.
After approximately twenty minutes exposure the fungus cultures were removed. Samples of ozone decay light exposed
cultures of fungus were placed on new growth media and cultured. The new cultures showed no spore formation,
only mycelium growth. These new
cultures were likewise transplanted to new growth medium for over ten
transplant generations and only mycelium growth was observed, but no spore
formation. This phenomenon may well
explain why pumping large amounts of ozonated air into basements, under houses,
and inside walls can either greatly reduce or generally eliminate health
problems from the spores of molds and fungi.
Merlin Wolf also evaluated for his
company the use of ozone in semiconductor clean room fabrication processes to
control and eliminate air born organic micro particulate. In a linear series of adjacent clean rooms
separated/partitioned by large glass windows/walls, one clean room had a
maintained constant ozone concentration level and the micro particulate count
was monitored verses time. Not only did
the micro particulate count continually and rather significantly decrease in
the ozone clean room, but also in all of the adjacent rooms. The nearer the clean room to the ozone clean
room, the faster the micro particulate count went down. All surfaces including dust particle
surfaces have a ultra thin layer of physically adsorbed oxygen and water
molecules. When the physically adsorbed
oxygen molecules on the dust surface absorb the meta-stable oxygen molecule
decay light, it goes into a meta-stable state which is exceedingly chemically
reactive and reacts to oxidize on the particle surface. Of course the oxygen in the room air also
absorbs the decay light and goes into the meta-stable state which reacts with
dust particles. In the case of organic
dust particles, generally carbon dioxide, sulfur and nitrogen containing gases
and water are formed. Over time with
ozone decay light exposure, the organic dust particle is converted to gas and
disappears. The common surfaces we come
into contact with each day have all kinds of spores, viruses, and bacteria on
them. These spores, viruses, and
bacteria also have an ultra thin layer of continually renewed physically absorb
oxygen and water. And they to can be
“dissolved” away by interaction with ozone decay light. All house and hospital surfaces could be
disinfected of these microbes by either the use of direct ozone at very low and
very safe concentration levels and or ozone decay light by its self. Special, yet to be invented, high frequency
gas light tubes that also generate meta-stable oxygen decay light (ozone decay light) could replace some of
the common high frequency fluorescent light bulbs/tubes in hospitals and homes.
Infra Red LED Light
Therapy- The top end of the infra red
spectrum is very useful at exciting various enzymes and proteins in the body to
be able to carry out useful functions.
In particular enzymes in the respiratory chain that produce ATP can
absorb top end infra red light and use it to increase their rate of ATP
production rather significantly. ATP is
the key to all tissue repair processes.
You can go onto the Google search engine and find large numbers of
research papers on how to use infra red LED light to treat all kinds of
conditions. Also, you can find lots of
web sites to sell you infra red LED products for experimental medical
treatment.
Magnetic Field
Therapy- It is empirically known that
intense static magnetic fields ( 5,000
gauss + ) can have a very therapeutic
value for various health conditions , i.e. Alzheimer’s Disease, General Brain
Injury, Muscular Dystrophy, Multiple Sclerosis, Parkinson’s, Stroke Impairment,
Sports Injuries, Back, Knee and Joint Problems. (ref. 11). From
scientific research it is known that static magnetic fields speed up many
enzyme reaction rates (ref. 3). In
particular key enzymes involved in ATP production.
From what has been stated above, it can
be inferred that a judicious combination of negative oxygen molecule ion
therapy, ozone decay light therapy, infra red LED light therapy and static magnetic field therapy can
achieve greatly enhanced ATP production, which facilitates tissue regeneration
and repair (healing). Below will be
presented a proposed set of experimental physical constructs to achieve the
above stated judicious combination of modalities.
Physical
Hardware for Increasing ATP Production
Each alternative health practitioner that
attempts/tries out the various treatment modalities discussed here will do it
in their own way. This is due to
available treatment space, financial resources available, technical/hands on
ability, and personal preferences. I
will give you my thoughts on application to practice and the rest is up to the
practitioner and their associates and their patients to experiment with.
1) Artificial
Magnetic Field Environment - By laying
down a large number of insulated wire turns onto the boundary of the
area/region (perhaps an entire room or building) being used for treatment and
running a very smooth D.C. current through this coil, a rather significant
increase in magnetic field can be achieved inside the treatment area. It is
nearly essential that the generated magnetic field be of approximately the same
polarization (direction) in the treatment area as the earth magnetic field is
in the treatment area. For example, in
the Los Angeles area the earth’s magnetic field enters the ground or has a dip
angle of approximately 58 degrees below the horizontal. And the horizontal magnetic field component
points approximately to the earth’s geographic north pole, which is in the
approximate direction of the earth’s south magnetic pole. Dr. Dean Bonlie who has worked extensively
in treating patients with intense ( 5,000 gauss +) magnetic fields has found or
determined that the patient’s body and particularly their mitochondria are
apparently magnetically polarized or their substructures reordered by the earth’s magnetic field while they
sleep. It is during this polarized
sleeping period that the body does much or most of it repair and maintenance
work, while having the earth’s magnetic field significantly increase the enzyme
reaction rate of the key enzymes involved in ATP production. For magnetic field therapy the patient
should be oriented in the magnetic field such that it is approximately (within
plus or minus 45 degrees of) the same orientation the patient experiences while
sleeping in their bed in the earth’s magnetic field. For example some people sleep mainly on their back, some on their
side, some on their right side, and some on their belly. Some people sleep with their head pointing
north, some pointing east, some etc..
In other words when using the static magnetic field treatment on the
patient, have the patient positioned in the magnetic field as they were home
sleeping. Without the earth magnetic
field, people would produce significantly less ATP and have a compromised
immune system. When people get out of
bed and continually move around during the day, the magnetic polarization in
the body from the sleeping in a particular orientation in the earth’s magnetic
field has a persistence.
The magnetic field treatment option
for increased ATP production is a bit tricky to implement due to potentially
detrimental effects outside the coil perimeter. Outside the coil perimeter the magnetic field is reversed in
direction to that inside the coil.
Therefore the artificial magnetic field outside the coil tends to cancel
out the earth’s magnetic field and leave in it’s place a reversal field
polarity, or a null field or a weaker field depending on the distance from the
coil and the strength of field generated by the coil. This affect is a serious health concern for at least several coil
diameters away from the coil edge. For
example imagine that an entire treatment room perimeter had a coil on it. Now all the rooms on the other side of the wall
from this treatment room would have magnetic fields approximately opposite to
the earth’s magnetic field with a varying of magnetic field strength across
this room and rooms adjacent to them.
Over the long term this situation could potentially cause health
problems for people inhabiting these rooms.
For this reason if the magnetic field option is going to be attempted,
it is best to have the magnetic treatment room/house isolated away from other
work/treatment areas. You will need to
find a physics teacher or student to help you design your coil and DC power
supply. The DC power output needs to be
very low ripple (smooth). The other
option is to obtain magnetic sleep pads and treat the patients on these sleep
pads. The magnetic fields from the sleep
pads are very localized. Such magnetic
sleep pads are obtainable from Magnetic Co (1-800-265-1119).
2) Negative Oxygen Molecule Ion
Generation, Confinement,
and Absorption - By placing several negative ion generators
into the enclosed treatment area a high concentration of negatively charged
oxygen molecules can be built up in the air of the treatment area. Then by having the patient hold onto, sit on
or lay on ( make a good electrical contact with the body surface ) a low voltage (+40 to +160 volts) high
impedance (10 meg ohm to 20 meg ohm resistance) positively charged surface
(electrode), the patient can attract to their body surface copious amounts of
negatively charged oxygen molecules to be absorbed both through the lungs and
acupuncture points. This circuit with
electrically conducting fabric is soon to be available at rifeenergymedicine.com under the name Oxygen Ion
Energizer. The patient needs to be in
contact with the positive surface (electrode).
The reasons for this electrode connection are two fold. One is to take away electrons and thereby
charge the body surface to a positive voltage, which will draw into the body
surface negative oxygen molecule ions.
The second is to not build up a negative charge from taking in
negatively charged oxygen molecules until the build up of negative charge on
the body surface repels any more negative ions from reaching the body
surface. The practitioner needs to be
aware of the need to also be earth grounded or charge themselves up like the
patient, if they are going to be in the treatment area for long.
Acupuncture points are designed to take
in negatively charged oxygen molecules and place them into the meridian system
network for distribution to body organs and tissue See Figure 5C). Figure 5D shows a twenty four hour meridian “energy” supply
to body organs chart. Each major organ
has a two hour period in which it is the major receptacle of “energy”
(negatively charged oxygen molecules) from the meridian system. Furthermore, that same organ has another two
hour period twelve hours away from the major one hour period in which it also
receives a larger than normal supply of the “energy” from the meridian
system. This twenty four hour clock
chart for the organs is sun rise and sun down calibrated. Midnight on the chart would be half way
between sun down and sun rise time.
Therefore, the chart times are always changing compared to normal clock
time, since sun rise and sun down continually change compared to normal clock
time throughout the year. Also two
other conditions are at play, namely your location in your in your time zone
and are you on day light savings time or not?
The important message to get from this meridian organ chart is that
depending upon what the patient’s problems are it might be best to treat the
patient with negative ion therapy during one of the major or minor one hour
periods in which the involved or concerned organ(s) gets its main attention
from the meridian system.
Measurements by ultra high impedance
volt meters show that acupuncture points usually maintain a positive voltage of
5 to 10 volts relative to the body’s average voltage, i.e. compared to the
potential from an electrode connected to the brachial plexus. The body has/maintains a bi-polar
charge/voltage distribution on its surface ( see Figures 6). This
bi-polar charge/voltage distribution flips polarity back and forth about every
15 to 20 minutes. The negatively
charged side of the body draws in positive ions such as CO2+
and O2+ and the positively charged side draws in negative ions such as O2-. These negative ions then migrate over the
body surface under the influence of the weak , but significant voltage gradient
on the body surface until they reach a acupuncture point and are absorbed. The CO2+ and O2+ accept electrons from the body
surface and or the air passages and lungs and become CO2 and O2. This removal of electrons from the body surface allows the body
to maintain one body side at a relatively positive charge for negative ion
attraction. A key point to understand
is that if the body surface is not being maintained at some positive voltage by
some external device, then there is a need for both positive and negative ions
to be present in roughly similar amounts.
The main sources of positive and
negative ions in our normal environment are sun light (photo ionization),
cosmic rays, natural background radiation from the break down of trace amounts
of radioactive isotopes in the environment, pine needles in the mountains,
which can produce copious amounts of negative ions. The main source of ions for the great majority of people is the
break down of radioactive isotopes. The
various radioactive isotopes during break down commonly emit high energy (fast)
electrons, high energy (fast) protons, and high energy (fast) alpha
particles. As these high energy
particles pass through the air they make many thousands of collisions with air
molecules breaking them up into positive and negative ions. Some of the main resultant ions generated
are O2- ,O2+,and CO2+. The O2- is absorbed by
acupuncture points on animals and CO2+ is taken in by
stomata on the bottom side of plant leaves which are negatively charged
compared to the top of the leave side.
Near the surface of the earth the positive ions concentration generally
is significantly greater then the negative ion concentration. This is do to the earth surface having a net
220,000 volt negative charge and the bottom of the ionosphere having a 220,000
volts positive charge. The ions
generated at the earth surface find themselves in between two charged surfaces. The positive ions (CO2+)
remain near or go toward and collect at the negative surface (the earth
surface) and the negative ions (O2-) go toward the
ionosphere. Animals by having a dipole
electric field on their surfaces are able to draw onto themselves both CO2+
and O2-.
3) Ozone Decay Light Treatment - >Let us
assume the treatment area is a room of lets say 20 ft. X 15 ft. X 8 ft.. It should be a relatively easy matter to
have a large mirror ( 6 ft. X 6 ft. ) placed on the ceiling or wall and have it
sealed in air tight with a wooden surrounding frame and transparent glass
window. (Do not use silicon as a
sealant. Use an epoxy.) The mirror and glass window can be made from
one or more mirrors or glass windows as long as the enclosure is air
tight. This could also be done in a
much smaller room or enclosure for patient privacy and treatment convenience,
i.e. a large closet (see Figure 7 and Figure 8).
The distance from the mirror surface to
the glass window should be about one foot.
Ozonated air is fed into the enclosure from a corner and it leaves from
the opposite diagonal corner through a hose that feeds back into the ozone
resistant air pump that feeds the ozone generator or that vents to the outside
world or perhaps into a jacuzzi or swimming pool. When the meta-stable oxygen generated from the ozone decay
process goes to the ground state (see Figure 4), it emits
infra red light from the top end of the infra red spectrum, which passes
through the window glass onto the patient who is in their under ware or nude
and therefore exposing their skin to near maximum amount of ozone decay
light. The closer the patient to the
window the better. Note: Do not have any other mirrors face off
directly against the mirror in the ozone decay light box. This would cause a laser action effect that
would greatly decrease or destroy the
desired result of increased ATP production and anti-microbial action. Additional mirrors for concentrating the
decay light on one person should make an angle of at least 60 deg. with the
mirror in the ozone decay chamber (see Figure 8).
Another method for getting ozone decay
light benefits is to be ozone body bagged.
That is the patient gets into a specially constructed body bag or tent,
while in the nude with only their head sticking out. Strongly ozonated air is pumped into the body bag or tent and the
bag swells up creating a volume of ozonated air which has ozone decaying and
meta-stable oxygen going to the ground state releasing infra red light. If the inside of the bag or tent is a
non-oxidizing light reflective surface better and quicker results can be
obtained. This ozone bagging will need
to be carried out in a well ventilated room.
Still another method for meta-stable
oxygen decay light to be generated is with an ozone decay light laser. This meta-stable oxygen laser produces a beam
of Infra Red light from the top of the infra red light spectrum which can be shown onto an infected or
injured area of the body (see Figure 9). This
infra red laser light can both create meta-stable oxygen molecules to fight
infection in the tissue while at the same time greatly accelerate oxygen
transport into cells for accelerated ATP production and associated accelerated
tissue repair. An experimental ozone
decay light laser will soon be available by commissioning agreement through
rifeenergymedicine.com.
OVERVIEW
OF TREATMENT MODALITIES FOR DESTROYING MICROBES
Many diseases and ill health conditions
are microbe driven. Sometimes these
microbe infections are easily recognized and well known. Other times these infections are very hard
to detect and are not recognized as being present. Apparently much of what is considered normal aging and normal
aging health problems are actually low grade long term microbe infections. With these non-detected and or unsuspected
long term low grade infections eliminated, the patient quite often experiences
a renewed vigor for life with the energy and endurance to pursue life to it’s
fullest.
Below are listed five energy based
treatment modalities for destroying microbes in human/animal tissue. A brief description of each of these
modalities is given along with references for future research and study. The practitioner should by now realize that
longer overall treatment times will be necessary for most patients on many of
their office visits. It may well become
desirable to have evening and late night treatment sessions a couple or so days
a week to take advantage of the working of the meridian system.
1) Low
Intensity Broad Band Ultrasound Treatment-
The fundamental point to understand is that every microbe that Dr. Royal
Raymond Rife worked with had at least one frequency of mechanical vibration
(sound/ultrasound) that killed it very easily using a very low intensity of
sound/ultrasound.
Today, there are fairly large lists of so-called Rife
frequencies available on the internet that are used by various voltage square
wave devices/machines which have been moderately successful in treating a long
list of conditions. These are machines
in which the patient generally holds onto cylindrical electrodes or sits on or
stands on pads, etc.. However, the
frequencies used by these machines are not in general the frequencies Dr. Rife
used in destroying the microbes Rife worked with using his frequency
instrument. There are many conditions
for which these frequencies are not very effective. And, there are many conditions for which no frequencies are known
at all.
To overcome these shortcomings an
ultrasound generation machine is needed that slowly scans through all of the
frequency range that Rife was known to have worked with and then some. Just such a machine is the experimental low
intensity broad band ultrasound unit, the ULTRA 10A. The ULTRA 10A by using various voltage wave form patterns
applied to a piezoelectric element produces complex harmonic patterns
(frequency sets) of sound/ultrasound.
By slowly changing the frequencies of the voltage wave form patterns, the
complex harmonic frequency patterns of sound/ultrasound produced by the
piezoelectric element can be slowly varied.
In other words, by the proper choice of voltage wave form scanning
patterns applied to a piezoelectric transducer element, the entire range of
ultrasound frequencies used by Rife in his research and then some can be
generated. If you do not know the
frequency of the ultrasound that kills the microbe, it does not matter as long
as you can scan through that ultrasound frequency at a slow enough rate and at
some associated minimum intensity to do
the job of killing/disabling that microbe.
2) Microbe
and Viral Treatment with Ozone Decay Light -
When ozone decays, it breaks apart into a single oxygen atom and a
oxygen molecule of two bound together oxygen atoms (see Figure 4). The
single oxygen atom is very chemically reactive and quickly reacts with
something. The oxygen molecule coming
from ozone decay is often in an excited meta-stable state. The meta-stable oxygen molecule is
exceedingly more chemically reactive
then the normal oxygen molecule and very anti-microbial. Aerobic and anaerobic bacteria as well as
viruses are very susceptible to damage and destruction by both meta-stable
oxygen molecules and single oxygen atoms.
The oxygen molecule has two such meta-stable states, one of which has a half life in air of
approximately 8 seconds (the Sigma state) and the other a half life in air of
approximately 45 minutes (the delta state).
When these excited meta-stable states decay to the ground state, they
emit an infra red light photon from the top end of the infra red spectrum. Namely, 762 nm for the Sigma state going to
the ground state and 1,275 nm for the delta state going to the ground
state. When this light goes into the
body tissue, it has a fair probability of being absorbed by a oxygen
molecule. That oxygen molecule which
absorbs this light goes into the meta-stable state. By having the patient lay/stand in front of a strong ozone decay
light source in their under ware, significant meta-stable oxygen can be
generated inside the body of the patient and a microbe die off can be
expected. For more localized treatment
of an infected area or an area that needs tissue regeneration, a experimental
low intensity meta-stable oxygen molecule laser can be used. An experimental low intensity meta-stable
oxygen laser will be soon available by commissioning agreement from
rifeenergymedicine.com.
3) High
Intensity “Color” Therapy - Many
viruses and bacteria are susceptible to disruption and destruction by specific
light frequency ranges for each specific microbe. By using one or more high pressure mercury arc lamp source(s) and
then putting light color filters on it (narrow band infra red filters are
included), a light source is generatede that will destroy and or disrupt
specific viruses and bacteria (see Figure 10 ). For
detailed information consult the article,
DNA DISRUPTION IN VIRUSES AND
ANIMALS BY THE USE OF SPECIFIC FREQUENCIES OF ELECTROMAGNETIC RADIATION WHICH
MATCH THE RESONANCE FREQUENCXIES OF THE DNA SECTION WHEN THE DNA SECTION IS
CONSIDERED AS AN ELECTRICALLY CONDUCTIVE ANTANA STRUCTURE By Gary Wade,
Physicist, 12/29/02 , on the web site rifeenergymedicine.com. Note that even a light frequency that is a
fair amount off the ideal resonance frequency and or its harmonics for the
virus/microbe in question can still deactivate the virus/microbe as long as the
light has a relatively narrow frequency spread (a relatively pure
“color”). You can obtain viral DNA
genome length information to be used in needed light frequency calculations,
at nebi.nim.nih.gov/pmgifs/genomes/vis.html
. The velocity (V) of the electrical
wave on the DNA is approximately equal to: V = 1 / (LC)1/2; where L
is the inductance per unit length and C is the capacitance per unit
length. In general the L and C values
are unknown or not well known.
A patient should be exposed to
such a light source while in their under ware or nature suit. The exposure should be for something like
ten minutes or so while the patient attempts to get their entire body surface
exposed to the light and in particular any obviously infected regions.
To get a whole new way to see how light
can be used for treatment of health
problems, it would be a particularly good idea to look into the work of Darius
Dinshah. I recommend the book, LET
THERE BE LIGHT, by Darius Dinshah, ISBN # 0-933917-00-7.
4) Charge
Density Wave Therapy - Charge density
waves are a moving compaction or rarefaction of ion density in an ionic
medium. For example your body’s blood
plasma and interstitial fluids are a salt solution similar to ocean water. The blood plasma and interstitial fluids are
full of all kinds of positive and negative ions (Na+, K+,
Cl-, Mg++, Ca++, HCO2-, OH-,
etc.). By applying a rapidly changing
electric field to the boundary layer (your dead skin) of the salt solution,
moving compaction and rarefaction waves (charge density waves) in the salt
solution can be generated. These charge
density waves can have rather strong electric fields associated with the
interface between the moving charge density wave front and the undisturbed
ionic medium. As a specific example
consider the case where a person is holding on to a cylindrical metal electrode
in each hand. Let one electrode be at a
positive voltage ( positively charged ) and the other be at a negative voltage
( negatively charged ). The positive
electrode will attract a layer of negative ions to the other side of the dead
skin layer from the electrode and repel the positive ions a little back into
solution away from the dead skin layer.
A similar situation will occur at the negative electrode region, except
there will be a reversal of the ion types displaced. Now, if the polarity of the electrodes are rapidly reversed
(negative electrode becomes a positive electrode and visa versa) there will be
a reordering of the ions facing off against the electrodes. The formally positive electrode will now
repel the negative ion layer away causing a negative ion charge density wave (
a charge density compression wave) to
move away from the dead skin layer into the body. Because the electrode is now charging up to a negative voltage it
will draw in a positive ion layer to face off against it. However, the positive ions moving toward the
dead skin layer leave a depletion of positive ions from where they moved
from. Other adjacent positive ions fill
in their former space. In turn these
positive ions have their former space filled in by adjacent positive ions. And
so on and so forth. This is a charge
density depletion wave. Both the compression
and depletion charge density waves have electric fields at their interface to
the medium through which they are moving.
The strength of these electric fields is determined by how fast the
polarity flip/reversal is completed and the magnitude of the voltage used. If the electric field is strong enough it
can interact with proteins in the blood, on virus surfaces, and on bacteria
surfaces and rearrange their structures so they no longer perform their normal
function. In general proteins in living
systems are strings of amino acids that are folded up into specific
configurations and are held in these configurations by cross liking hydrogen
bonds and short range van der Wall forces.
These hydrogen bonds are very weak chemical bonds. The proteins have various net positive and net negatively charged regions
on them. The electric field of the
moving charge density wave interacts with these net charge regions and puts
forces on these protein molecules. If
the forces are high enough hydrogen bonds can be broken and the protein
rearranges itself. In general the size,
shape, and specific charge configuration of a specific protein is crucial to
the proper functioning of that protein.
For example, in South America when a person gets bitten by a poisonous snake,
they pull a spark plug wire off the car and shock the holly crap out of the
bite region (ref. 11). The charge density wave electric fields rearrange the
snake venom proteins into relatively harmless proteins (see Figure 11). In a
similar fashion, as a charge density wave overcomes a virus the electric field
of the charge density wave can rearrange the virus surface proteins responsible
for attachment of the virus to the target cell. With these surface attachment proteins non-functional the virus
can not infect new cells. Similarly,
when charge density waves pass over the surface of bacteria they can denature
delicate bacteria proteins used by and often essential for bacteria’s on going
proper functioning and continued existence.
There are several forms of charge
density wave generation devices available.
One of them is a de-rated stun gun which has had it’s output voltage
lowered to approximately 25 thousand volts from 80+ thousand volts. This stun gun is used mainly for snake
bites, but can also be used for spider bites and insect bites. Another tried and true device is Edgar
Cayce’s Violet Ray. The Violet Ray
device produces not only charge density waves, but also ozone, negative oxygen
molecule ions, and bottom end of ultra violet light spectrum light. The Violet Ray is often found to be very
useful in treating insect and spider bites, skin infections, inflammation and
soreness in muscle and joint tissue.
The Violet Ray can be purchased on the internet. A third device is the Wolf Tech. It is very similar to the Violet Ray, but is
much smaller in size and is battery operated.
It is a great device for the practitioner to have in their pocket.
(The Wolf Tech can be
found at
http://braintuner.com/electroacu.htm#Wolf-Tek)
5)
Pulsed Ringing Magnetic Field Therapy for
Microbial Control
The
rapid discharge of a high voltage capacitor through a coil of wire can produce
anti microbial phenomena. If the
capacitance of the capacitor and the inductance of the coil of wire are chosen
properly, they can produce a high frequency oscillating magnetic field when
wired together through spark gaps. The
rapidly changing magnetic field produces strong electric fields in the space
around the coil. And these electric
fields are also rapidly changing in strength.
The electric field will produce charge density waves in the body’s
electrolytic juices and eddy currents throughout the body tissue. We have already discussed the charge density
waves. The electrical eddy currents
when they enter the range of 100 microamperes per square centimeter to 200,000
microamperes per square centimeter they begin to biologically deactivate all
manor of viruses and microbes as discussed in U.S. Patent # 5,188,738. The properly designed magnetic pulse units are very
useful for fighting microbial and viral infections while at the same time
promoting tissue repair.
For Tissue Repair After Infections Are Under
Control
Pulsed Magnetic Field Therapy – Many phenomena occur when animal tissue is
exposed to rapidly changing magnetic fields.
Which phenomenon is most observed depends on the strength, rate of
change of, and duration of change of, the magnetic field. As discussed above these charge density
waves and electrical eddy currents can be very anti microbial. Another useful
and interesting phenomenon that can be caused by a repeatedly pulsed magnetic
field is dedifferentiation of fibroblast cells and some types of precursor
endothelial cell types into embryonic looking cells. This dedifferentiation of fibroblast cells is very
important. When a person suffers
severe/traumatic physical injury, i.e. tissue damage, fibroblast cells, which
normally are dispersed in the body fatty tissue and circulate in the blood,
migrate to and accumulate at the damaged tissue site to form an emergency
tissue patch. If the damage is not to
severe the injury will be nearly fully repaired with only minor scar tissue
remaining in the area. The scar tissue
is mainly made up of fibroblast cells that have laid down and are maintaining a
tough collagen protein fiber matrix, which holds all the surrounding tissue
together. When these cells are made to
dedifferentiate by exposure to the appropriate pulsed magnetic field, while
they are part of and are maintaining scar tissue or damaged tissue soon to
become scar tissue, the result is that some of the cells do not go back to
being fibroblast and endothelial cells.
Instead they become the type of cell that should be there at their
location in the damaged tissue or on the scar tissue edge, if the damaged
tissue or scar tissue were not there.
By exposing the damaged tissue or scar tissue to repeated pulsed
magnetic fields for approximately 5 to 15 minutes varying from twice every day
to once every other day for approximately one to six weeks often much of the
damaged tissue or scar tissue can apparently
be repaired/ removed and be replaced with normal healthy tissue.
The fibroblast and endothelial cells are
believed to be made to go embryonic due to drastic changes in ionic
concentrations in the cell cytoplasm and therefore the cell nucleus. These ionic concentrations react with the
cell DNA and DNA coupling proteins opening up some gene sets and closing down
others. It is apparently the rapid
onset of a strong pulsed electric field generated by the pulsed magnetic field
which causes some cell ion gate types to either open and or be set into their
natural mechanical resonate vibration mode which effectively makes the gates
open and then can be forced fed ions by the same oscillating electric field
(see Figure 12, Figure 13B, and Figure 14).
Experiments that I conducted at the Center for Complex Infectious
Diseases showed a relatively wide range
of combinations of range of pulsed electric field rise times, pulsed electric
field strengths, electric field pulse time widths, pulse rates, and total time
of exposure to pulses that could produce the desired results of having
fibroblast cells become embryonic looking and embryonic like in their behavior.
An experimental pulsed magnetic field
generator device for experimental treatment of damaged tissue (scar tissue) and
damaged tissue that is in danger of becoming scar tissue will soon be available
by commissioning agreement from rifeenergymedicine.com. It is recommended for experimental treatment
on joint and cartilage damage, tendon damage, ligament damage, adhesions from
surgery and traumatic accidents, i.e. sports injuries and car crashes. It is also for experimental treatment of
infections. It is recommended that
veterinarians experiment with this technology, in particular on such large
animals as horses that are often very difficult to work on by other methods for
the problems mentioned above.
Conclusion
An alternative health practitioner can
physically modify their office with various energy medicine therapeutic devices
and setups. This will allow the
practitioner to evaluate their patient’s needs and apply a treatment protocol
that can quickly show very positive healing results. Conditions which before were near hopeless or would take an
exceedingly long time to resolve can be remedied or alleviated relatively
quickly. The overall health level and
vitality of the patient can be brought to a whole new level, which the patient
may not have experienced since their youth.
Editorial note
Of course no matter how good the energy
medicine technology used is, the patient has to have an adequate balanced
nutritional intake to take full advantage of energy medicine technology. Unfortunately much of the American
industrial food supply is grossly lacking in nutritional value. It is very short on vital minerals,
vitamins, and essential oils. This is a
result of mineral depleted soils throughout America. We have industrial food preparation processes that greatly
degrade food mineral, vitamin, and essential oil content. These nutritional degradation problems are
compounded by hundreds of rather more than questionable food additives, which
are known to be toxic and disruptive to the body’s biological
functions/chemistry. In particular,
Monosodium Glutamate (MSG) is slowly killing much of America. This MSG is hidden in processed foods under
40+ different names, so you will not catch on to what is being done to
you. You see besides all the terrible things MSG does to your
body biochemistry, it is also addictive.
This allows the processed food manufacturers to knowingly produce a very
nutritionally poor “food” which you will want to consume a lot of because of
the addictive MSG content.
Let us not forget fluoride. We have the fluoridation of approximately
half the drinking water supply in America.
The basis for fluoridating the water supply is based on fraudulent
research and dishonest representations of the research. The cancer rate climbs by 1% per year in
every city/water district once the drinking water has been fluoridated by 1
ppm. This fluoride poisoning of America
is being promoted by the aluminum industry, the fertilizer industry, the American
Dental Association, and the U.S. Public Health Service. For any competent researcher the evidence
against fluoride use in drinking water
is overwhelming. What is required is a
class action law suit against those responsible for this would be crime. We need judgments against those responsible
similar to those against the tobacco companies.
Special Interest / Greed Medicine
In the first part of the twentieth
century the allopathic medical system became the dominant medical system in
America. This occurred through
financial support from pharmaceutical companies and concurrent political
lobbing to make and change laws to favor allopathic medicine. The American Medical Association under the
control and leadership of Dr. Morris Fishbein gained full control (hegemony)
over illness/health care in America.
All other alternative medical systems and treatment modalities other
than drugs, radiation, and surgery were effectively suppressed. Electro medicine was effectively destroyed,
i.e. I have in my library an electro medicine article from 1926 (replete with
electrical circuit drawings) in which all manor of diseases including cancer
were successfully being treated by Dr. Abrams’ Oscilloclast. The political and legislative actions of the
AMA suppressed and removed all such technology from medical practice. It is time to reform the AMA and it’s
control over medical school curriculum and licensing. It is time to supplant pharmaceutical medicine with alternative
energy based forms of medical treatments.
Most allopathic doctors are now open to investigating some forms of
alternative energy medicine. They see
the clear need for other approaches in treatment, particularly in cancer
treatment. It is literally a sin
against humanity that over 11,000 people a week in America alone die horrible
deaths from cancer. If you read Barry
Lyon’s book, The Cancer Cure That Worked, you will see that this cancer death
rate is all because the USC School of Medicine Special Research Committee did
not release the 1934, 1935, and 1937 clinical trial reports to the public on
Dr. Royal Raymond Rife’s cure for cancer, which was approximately 95%
successful in treating so called terminal cancer.
When the people of Alberta Province in
Canada got fed up with the standard allopathic medicine offering, they had
their legislature add one paragraph into law, which freed the allopathic
practitioner to use alternative energy based medical treatments. That one paragraph is most reasonable and
fair. See if you do not agree.
“A registered practitioner shall not be
found guilty of unbecoming conduct or be found to be incapable or unfit to
practice medicine or osteopathy solely 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 prevailing
treatment.”
Now why has “your” state legislature not
put this paragraph into your state law books?
Why has your allopathic doctor, chiropractor, naturopath, etc. not been
freed to use alternative energy based medical treatment? Why don’t you contact your state legislature
and ask them to put this paragraph into your state law books? That is right, get off your ass and do
something about this disgraceful pharmaceutical medical system we are living
under. Help free up your doctor to
practice the best medicine they can for your benefit and the profits of the
pharmaceutical companies be damned.
IF YOU FOUND THIS ARTICLE OF REAL VALUE, PLEASE MAKE A HARD COPY WHILE STILL AVAILABLE.
References:
1) Use
Google search engine and put in: Hyperbaric oxygen treatment for stroke.
2) Personal
observations on stroke victim treated at The Advanced Magnetic Research
Institute in Laguna Nigiel, CA and other work done by Dr. Dean Bonlie of
Calgary, Alberta, Canada.
3) Magnetokinetic
Effects on Radical Pairs: A Paradigm
for Magnetic Field Interactions with Biological Systems at Lower Than Thermal
Energy by Jan Walleczah, Bioelectromagnetics Laboratory, Department of
Radiation Oncology, Medical Center – Ao38, Stanford University, Stanford, CA
94305- 5124.
4) Go
on Google and put in: Thermal Heterogeneity Within Human Atherosclerotic
Coronary Arteries Detected in Vivo.
5) Go
on Google and put in: Hyperbaric oxygen in treatment of multiple sclerosis.
6) Information
received in a Physics department coloqueim lecture in the mid 1970’s.
7) The
Body Electric by Robert O. Becker, M.D. and Gary Selden (see Chapter 4), ISBN
# 0-688-06971-1
8) Brewer,
A.K. and R. Passwater, Physics of the Cell Membrane. 1. The Role of the double Bond Energy states, Am Lab 6:59-72, 1974.
9) Brewer,
A.K. and R. Passwater, Physics of the Cell Membrane. 2. Flourescence and
Phosphorescence in Cell Analysis. Am
Lab 6: 19-29, 1974.
10)
The Ion Effect by Fred Soyka with Alan
Edmonds (ISBN # 0-553-20755-5).
11)
Work of Dr. Dean Bonlie carried out at
his clinics. Contact Dr. David
Stokesbary, M.D. , Director of Advanced Magnetic Research Institute in Laguna
Niguel, CA 92677, (949)-367-0877 or
AMRI.com.
12)
Lancet, July 26, 1986, pg 229.
13)
Go to rifeenergymedicine.com and
read: Exciting Possibilities in Pulsed,
Intense, Magnetic Field Therapy: A Physicist View by Gary Wade.