A must read, would the drug companies be happy about this one?
http://abovetopsecret.com/bmrg.html

Purpose:

Killing Pathological Micro-organisms. The Biological Molecular Resonance
Generator (BMRG) radiates a complex electromagnetic signal through the
entire human body, which selectively destroys the enzymes and other
biological molecules unique to viruses, bacteria, amoebas, spirochetes,
and other micro-organisms. AIDS, Ebola, Hanta, Dengue, Plague, Cholera,
Polio, Strep, Pneumonia, Staph, Syphilis, Human Papilloma Virus (HPV)
are some examples of the micro-organisms which could be selectively
destroyed inside the living human without harming the body itself.

Other Benefits:

In addition to destroying pathological micro-organisms, in later
generations of the invention, the BMRG technology should be able to
destroy defective genes, destroy cancer cells, correct the function of
defective enzymes allowing the return to health for the sick and dying,
and stimulate the release of toxic substances from the bodies of
environmental illness victims.

Description of BMRG operation:

The BMRG acts as both a diagnostic, and a treating instrument. The BMRG
Skin Conduction unit is a portable system and uses 4 or more adhesive
skin electrodes to send electrical current at multiple frequencies
through the body. A hospital, or clinic based BMRG unit requires that
the patient be placed between two large panels where an electric field
comprised of multiple frequencies are passed through his/her body. The
operator of the BMRG would control the instrument through a
"Windows"-based computer program interface. The first phase of treatment
would be a diagnostic "scan" of the patient. Then, treatment of the
patient would immediately
follow. After treatment, a follow-up "scan" would be made to determine
that the treatment had been effective. A secondary treatment and re-test
would be administered if it was indicated.

Detailed description of BMRG operation:

The first stage of the procedure is to run the machine in a Diagnosis
Mode. In this phase, the body is radiated with a wide spectrum of low
power currents or electric fields. The machine will measure the body's
response to the frequencies, and determine the frequency vs. power
absorption profile of the body. A power absorption spike at a certain
frequency would indicate the presence of a molecular bond which
resonates at that frequency. The frequency vs. Power Absorption profile
is referred to as a "frequency signature" of the body. The patient's
frequency signature will then be fed to a computer for analysis. A bank
of "disease frequency signatures" will be compared with the patient's
frequency signature. The disease frequency signatures will be determined
using
various techniques and be ready for comparison in the diagnostic phase
of the BMRG operation. If a disease frequency signature is detected, the
patient will be treated with selected subsets of the disease frequency
signature. Having determined the appropriate treatment frequency
signature, the Treatment Phase will begin. The microbe's frequency
signature is then applied to the body through the skin electrodes or via
the air between the two electrodynamic panels. These frequencies will be
supplied to the patient with enough power so as to destroy the
biological activity of the specific molecules which are unique to the
micro-organism. The patient
will be virtually unharmed because the power of any one frequency will
be small, but the additive power associated with the multiple
frequencies directed at specific molecules within this pathologic
organism will be sufficient to break the conformational bonds upon which
its enzymatic functionality depends.

Theory of Operation:

An oscillating current or Electric field will be impressed across the
human body at low power levels to diagnose, and at higher power levels
to treat a person who has been infected by a microorganism. When a
molecular bond's resonant frequency is impressed upon a molecule, that
molecule will absorb energy from the field. Thus, it will be possible to
detect the presence of certain molecular bonds by noting the coupling of
the electric field with the body. This is done by various electronic
detection methods. There is a characteristic number of individual
frequencies which are absorbed by the human body, and another
characteristic set of frequencies
which are absorbed by the enzymes, DNA, RNA, and the other
macromolecules of a microbe's cellular machinery. A discovery and
research phase will be needed in the development of this technology to
catalogue the signatures of the numerous pathologic microbes. This
library of "frequency signatures" will be stored in the analysis
computer of the BMRG. By making a comparison between the patterns
detected in the diagnosis phase of the patient scan with the microbe
frequency signature library, the computer will be able to detect
patterns which indicate the presence of a certain disease microbe. Thus,
the BMRG will be able to make a
distinction between the characteristic signature of a human body which
is disease free and one which is infected. Once the infection has been
diagnosed, it is now possible to impress that set of frequencies upon
the human body. The frequencies chosen are the bond resonance
frequencies of the molecules which are targeted for destruction. The
method by which these microbial molecules are destroyed is as follows.
Nearly every large biological macromolecule has many points which have a
negative or positive electrical charge. An example of this phenomenon
can be seen with common tap water, H2O, which has a partial positive
electric charge on
its Hydrogen atoms, and a partial negative electric charge on its Oxygen
atom. Likewise, in the case of the complex biological macromolecule,
there are many positive and negative sites on and within it. These sites
of positive and negative electrical charge are the points which respond
to the pushing and pulling of the Electric field that is impressed upon
the body by the BMRG. When the pushing and pulling of a molecular bond
is applied at the resonant frequency of that bond, the Electric field
energy is absorbed by that bond. With each cycle of the Electric field,
the bond absorbs more energy and is deformed more. There will be some
loss of
energy to the surrounding molecular structure during this process, but
if sufficient power is supplied to overcome the energy loss rate, the
molecular bonds will be broken. Typically, the bonds holding the
constituent parts of the large macromolecules together are Hydrogen
bonds, and these are relatively weak bonds compared to the covalent
bonds which are used in making the sequential atomic backbone of the
molecule. Thus, since destruction of conformation is all that is
required to inactivate the microbial metabolism, only small amounts of
electrical energy, supplied at the resonant frequency of the
conformational bonds which are specific to the microbe need be used. An
additional effect will be utilized to focus the treatment on the desired
biological molecule which will make the treatment more specific and more
effective. Therefore heat energy will be added to the molecule due to
the energy absorbed by the resonant bonds, and the associated damage to
the target molecule will be additive, disruptive, and
de-conformationalizing. Again, the overall strategy is that energy is
applied to specific molecular bonds within the microbe, and those bonds
are then broken by the kinetic (heat) energy which they have absorbed.
The net effect is to break the low energy bonds which create the shape
of the molecule. The molecular shape is the aspect of the biochemistry
which ultimately produces the biological
effect. By permanently distorting the shape of the molecule, the
organism is functionally inactive, and may be cleaned up by normal
immune system action.


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