ANTI-AGING
AND ENERGY MEDICINE
By Gary Wade
(5/12/07)
ARE CONTINUOUS LOW GRADE SUB
CLINICAL VIRAL AND MICROBIAL INFECTIONS DETERMINING THE VELOCITY OF THE
PHYSIOLOGICAL AGING RATE AND THEREFORE PROBABLE LIFE EXPECTENCY FOR EACH
INDIVIDUAL (YOU)? AND IF SO WHAT CAN BE DONE ABOUT IT?
The short
answer is a qualified yes. Now
for the discussion to support the qualified yes and what can be done about it.
When the live blood of the average person is observed by high power optical
microscopes, a variety of bacteria or other microbes will be seen. If the blood
is cultured on the right growth media, those observed microbes and others will
be observed growing on the cultures. What is not observed in the blood
optically, except with very special ultra high power optical microscopes such
as a Rife type microscope (ref. 1,2,3), are the nano bacteria, the mycoplasma,
rickettsias, and viruses. All of these microbe types mentioned above can and
will lead to and cause continuous cellular death throughout the body. Let us examine
some of the ways this cellular death occurs including chemical poisoning.
Example 1 - Let us suppose an individual has a virus infection of some body
tissue or organ. In general the viral infection can be of two kinds. One where
the virus is of the type that takes over cellular machinery and produces so
many virus copies inside the cell that the cell swells up and ruptures open
releasing the viruses to go off and infect new cells and repeat the process. In
this process the infected cell dies and will need to be replaced. In the second
kind of viral infection, the virus takes over the cell machinery and produces
viruses that bud off the infected cell membrane and go on to infect new cells.
In this type of viral infection the infected cell is not directly killed by the
virus, but is generally not capable of carrying out it’s normal functions.
These infected cells are however killed by certain types of white blood cells
and will need to be replaced by the cell division of uninfected cells.
Example 2 -
Let us suppose an individual has a traumatic physical injury, such as a bicycle
crash, a car crash, a fall down the stairs, a sports injury, surgery, etc.. By
traumatic physical injury, I mean an injury where tissue is ripped and/or
ruptured. There will be bruising (internal bleeding) and torn tissue. The
various microbes found in the blood will after a traumatic physical injury have
access to new tissue damaged regions where the microbes can multiply greatly in
numbers (an infection) and kill/eat large numbers of cells, which will need
replacing after the infection is taken care of. Sometimes the low grade
infection at a injury site last for many years. With this traumatic physical
injury also comes the generation of scar tissue, which has it’s own set of problems,
which can be converted to a healing resource as will be discussed below.
Example 3 -
Suppose an individual takes in a toxic chemical(s) in their air or food or
drink, for example 1 ppm of fluoridated water. These toxic chemicals can over
time lead to significant cell disfunction and cell death in one or more tissue
sets in that individual’s body. These dead cells from chemical poisoning will
need to be replaced by other cells dividing. A great example of this sort of
poisoning is what is called chemotherapy for cancer patients, where the
standard allopathic medical treatment is often as bad or worse than the cancer
they are supposedly treating. Another good example is the fluoridation of
water. The fluoride ion for example is a general enzyme poison and disrupter.
No technically competent person would ever want to drink 1 ppm fluoridated
water, yet half of our country’s water supply has now been fluoridated. Perhaps
we need a lot less technically incompetent lawyers as our state legislators.
Once a city’s water supply has been fluoridated at 1 ppm the cancer rate goes
up by approximately 1% per year from then on in that city until cancer is a
given event for almost all people. This may well help explain why the cancer
rate in the U.S. has gone from around one in twenty in the first part of the
twentieth century to approaching one in two currently. The fluoridation
poisoning of water in the U.S. was started shortly after world war 2.
When cells in
any particular tissue location are killed or die off other cells in the
neighborhood start dividing to replace the lost cells and or stem like cells
migrate into the region to divide to replace the lost cells or pin point cells
as discovered and named by Dr. Rife move into the damaged area and become the
type of cell needed to replace lost cells (ref. 3). When these cells divide
their chromosomes loose approximately 50 to 80 telomeres from each end of each
chromosome, so that in both daughter cells resultant from the cell division
process, there are now 50 to 80 telomere unit lengths shorter at the ends of
the daughter cell chromosome ends. When these daughter cells divide again in
the future, the daughter cells from that cell division will loose another 50 to
80 telomeres from each end of each chromosome in both daughter cells. Over the
years as cell deaths continue to occur and cell division to replace lost cells
continues, the number of telomere units become smaller and smaller in number
until the daughter cells can no longer divide and do tissue repair, the person
begins the process of shriveling up and dying.
Shortly before
birth the baby has cells throughout it’s entire body that have chromosome
telomere tail lengths of around 2,000 telomere units. Each telomere unit
consists of a single strand of DNA made up of six genetic code bases (GGGTTA),
where A is adenine, T is thymine, and G is guanine. So we see that the person
only has so much growth and repair ability determined by their initial number
of telomere units at the end of each cell chromosome at birth. Furthermore, it
should be pointed out that cellular metabolism rate and therefore organ, gland
and tissue metabolism rates are apparently a function of telomere lengths
(number of telomere units) at both ends of the chromosomes. After the telomere
lengths shorten significantly from that of youth, the cellular metabolism and
hormonal secretion rates from various glands decreases significantly. What the
exact mechanism connection is not yet known. Once the telomere lengths have
shortened to a critical length the cell can no longer divide.
As we continue
this “normal aging process” of life where we are regularly exposed to toxic
chemicals and the very large number of viruses and microbes of the world, we
continually suffer cell death and cell replacement. However, we have only a
very finite ability to replace cells and maintain a adequate metabolism rate
for adequate immune system functioning. Over time (aging) one or more vital
organs or tissue sets can no longer adequately repair or maintain itself due to
telomere shortening fails, and you die. For example, cancer (failed immune
system), heart disease (infections in the heart and arteries), liver failure
(often viral caused or chemically induced, i.e. tylenol and alcohol used
together), kidney failure (often viral or bacterial infection or chemically
induced), etc..
The Fixes -
What can be done to slow down, halt, and reverse this “normal aging process”,
namely continuous cell death and cell division to replace lost cells? Some of
the answers to this question are probably known by the reader and some should
be quite a surprise. Most readers realize that good or proper nutrition is
essential for a healthy immune system and optimum cellular functioning. Good
nutrition in conjunction with high dosages of various vitamins, minerals and
supplements can halt and reverse degenerative diseases and greatly slow the
process of cell death from microbe infection and chemical poisons and therefore
slow down needed cell replacement. For example, as shown by the work of Dr. Fred
Klenner, M.D., Dr. Ewan Cameron, M.D., and two time Noble Prize winner Dr.
Linus Pauling, Ph.D., massive doses of vitamin C when used with the proper
treatment protocols, often including other supplements, can reverse many
degenerative diseases and rid the body of many types of virus and bacterial
infections(ref. 4). However, FDA officials at the behest of international
pharmaceutical companies have sold out and betrayed the American people by
signing off on Codex Alimentarius. Codex Alimentarius has the U.S.A. harmonize
its vitamin, mineral, and supplement availability and dosage amounts available
to that available in the European Union (E.U.). In the E.U. most supplements
are soon to be taken away and allowed vitamin and mineral dosages are being
reduced to ridiculously low levels. This is a direct result of actions from
international pharmaceutical companies. In my opinion the time is fast
approaching where the American people will need to organize, rise up and remove
the ownership/leadership of the pharmaceutical companies and purge the FDA of
the corrupt bureaucrats and purge congress of the corporate “elected” PAC
whores who have not done the people's business, but instead have continually
put corporate interests first. Is it not time for a nationwide reform movement
where the people take back the government from the control of corrupt corporate
interests, just as was done around the beginning of the twentieth century?
There are now
readily available various vibratory energy treatment devices available to help
clean out the body of various viral and microbial infections to the point that
the immune system can finish the job. The most common types are blood cleaning
devices like Bob Beck’s Zapper, various so called Rife Machines, pulsed
magnetic devices, light devices, and others.
The Bob Beck
Zapper is based on the Patent # 5,188,738 where it is disclosed that relatively
weak electric current flow through the blood can kill or deactivate the vast
majority of viruses and microbes. This type of blood cleansing technology has
apparently not been implemented into general use in hospitals due to its
effectiveness. Its general use would apparently drastically shorten patient
time spent in hospital. Also, its proper use would also apparently greatly
reduce further doctor office visits and prescription drug use. However, you
would think that the "powers that be" would at least have the decency
to use this patent to clean up blood for transfusions. But then again, the
"powers that be" are fine with over 10,000 people a week in the U.S.
dying horrible deaths of cancer, despite the work of Dr. Royal Raymond Rife.
The greed of the "powers that be" seems to have no bound.
There are
various kinds of so called Rife machines available. The varying success of
these machines is based on Dr. Royal Raymond Rife’s discovery that every virus
or microbe he studied, always had at least one frequency of mechanical
vibration (ultrasound) that destroyed the virus or microbe very easily and
quickly (ref. 5 ). By 1939 Dr. Rife had found the lethal frequencies of
ultrasound to kill the viruses and microbes associated with fifty two major
diseases, including the most common forms of cancer at that time (ref.6,7).
today the most common form of so called Rife machine is the voltage square wave
machines. These machines have two cylindrical electrodes you hold onto, one in
each hand, while the machine goes through various square wave voltage output
frequencies to treat the particular problem (ref.8). The best type of “Rife
Machine” for anti aging purposes is a broad band low intensity ultrasound
machine (ref.8). This type of machine scans through a frequency range from zero
to several tens of mega hertz of mechanical vibration (ultrasound). With
regular use this type of machine goes after all microbes and almost all virus
types to keep the viral and microbe load in the body at a minimum and therefore
a minimum of cell death rate occurring and minimum cell replacement rate is
needed.
There are many
pulsed magnetic field type devices available to experiment with. For our
purposes however, we are only interested in those that produce high frequency
ringing magnetic fields. For example, machines that have a wire coil of 8
inches internal diameter or larger that produce a transient oscillating magnetic
field that changes in strength at a rate of thousands of gauss per second and
the magnetic field polarity changes many tens of thousands of time per second,
each time power is pulsed into the coil. In other words a pulsed high frequency
ringing magnetic field. In my experimental work on pulsed ringing magnetic
fields of the type just mentioned, I have found several very useful and
beneficial effects (ref. 9). Namely, the production of in the body tissue
of charge density waves, and
oscillating electric eddy currents from a ringing electric field. Both of these
effects are anti microbial. The charge density waves, which are moving
compactions and rarifications of the normal positive and or negative ion
densities found in your body’s interstitial fluids which are salt water like.
These charge density waves can have a very strong electric field at the front
of the moving wave. This charge density wave front electric field can interact
with the delicate protein structures on viruses that are used to bind the virus
with target cell surface proteins. If the electric field is strong enough it
can interact with the various charged structures on these binding proteins and
rearrange their structure so that they can not bind to their target protein. If
the virus can not attach to the target cell surface, then the virus can not
infect the cell. The virus is effectively destroyed. This electric field can
also interact with bacteria surfaces and denature delicate protein structures
on them or reorganize their structure so that these vital surface protein
structures are non operational and the bacteria can not function normally and
in some cases probably starves to death. The ringing electric eddy currents
induced in the juices (essentially salt water) between and around tissue cells,
as discussed in the patent mentioned above, can deactivate all manor of viruses
and bacteria.
Another very
important discovery made with intense pulsed ringing magnetic fields was their
ability to make certain types of cells convert over into embryonic looking and
apparently embryonic acting cells. For example, in experiments I conducted at
Dr. John Martin’s Center for the study of Complex Infectious Diseases, I was
able to demonstrate that fibroblast cells and certain epithelial precursor cell
types could, with exposure to ringing magnetic fields of various field strength
and pulsing rate, be made to convert over into embryonic looking cells.
Furthermore, in field trials on horses and humans we were able to apparently
undo the effects of traumatic physical injuries where scar tissue had or was
forming. Empirically, it looks as though scar tissue which is formed by and
maintained by mainly fibroblast cells, was having the surface layer of
fibroblast cells on the scar surface converted to embryonic like cells that
then in turn converted over into the adjacent normal cell type the scar tissue
is butted up against. So, by daily repeated treatments with THE MAGNETIC PULSER
unit we were, judging from empirical evidence able to undo the great majority
of traumatic structural damage. In particular, in most cases, it proved to be
very quick (six to twelve 15 minute treatments) and easy to alleviate the pain
and discomfort from cartilage damage in joints, which would seem to imply
cartilage tissue re-growth and or repair (Ref. 9).
So far I have
essentially only discussed how to slow down the aging process by slowing down
cellular kill off using nutrition and technological devices to greatly lower
the viral and microbial load inside the body. However, there are at least two
methods to actually halt and reverse the aging process throughout the entire
body. Both of these methods of reversing the aging process use the enzyme
telomerase, who’s function is to put telomeres back onto both ends of each
chromosome in your cells. Before birth the genetic code information to make
telomerase is suppressed throughout the great majority of body cell types and
the body is therefore programed to die as discussed above. Scientists have now
succeeded in cell cultures in releasing/expressing telomerase and therefore
having cell cultures that do not go through the normal cell division and cell
death process that normal cell cultures go through. If these scientists can
succeed in finding drugs that can be taken up by all body cells in a well
controlled fashion, then it is possible to think of living for thousands of
years in very good health.
The other
method for releasing telomerase is an electromagnetic method. Namely, exposing
the body to specific frequencies of microwaves in the multi giga hertz
frequency range at low power levels for a brief time (a minute or less).
Experiments that indicated this method of producing telomerase were observed in
a set of experiments designed to regenerate animal tissue carried out in 1977
by a scientist friend of mine. It turns out that the great majority of animal
DNA is in the form of what is called B-DNA, which is a right handed double
helix that is electrically conductive. There is another form of DNA that is a
left handed double helix and is not electrically conductive. This left handed
electrically non conductive DNA is called Z-DNA and it appears on the
chromosomes in very short lengths at the beginning of gene sequences that are
designed to be all expressed together or not at all. The gene for telomerase
appears to be probably or possibly located in one or more of these gene
sequences that a Z-DNA is at the start of the gene sequence. The Z-DNA acts as
a blocker to expression (reading of) the gene sequence. The Z-DNA is created
out of B-DNA and maintained in the Z-DNA configuration by the interaction with
and complex together of the DNA with mainly specific positive metal ion/water
molecule complexes. If these Z-DNA sections have their ion/water complexes
removed from them, they convert back into B-DNA. If and when this occurs there
are promoter proteins sitting next to the former Z-DNA segment that move over
and complex with the newly formed B-DNA and form a start location and support
structure for the DNA reader enzyme to begin transcribing and expressing the
gene sequence so as to cause the generation of proteins and enzymes such as the
enzyme telomerase. So, the key to putting telomeres back on the ends of each
chromosome is to get specific the Z-DNA structure undone. The key to getting
the Z-DNA structure undone is to remove the ion/water complexes that are
complexing with the DNA base pairs making up the Z-DNA. There is in principle
an easy microwave exposure method to remove or disrupt the ion/water complexes
from complexing with the DNA base pairs. Since, Z-DNA is electrically non
conductive and various proteins that complex with specific sequences of the
chromosome DNA strongly effect the electrical conductivity of B-DNA at that
location, the chromosome can be thought of as a thin wire that has been
partitioned into a set of short electrically conductive sections that are
connected together by insulators (Z-DNA) and resistors (various DNA
complexing/coupling proteins). If each of these short electrically conductive
sections are treated as a half wave antenna and are exposed to their
fundamental resonance frequency of electromagnetic radiation, then standing
wave electrical oscillations can be made to build in amplitude on these B-DNA
sections. If these oscillating electrical waves build to an adequate amplitude
level, the associated oscillating electric field at the ends of these B-DNA
sections next to the Z-DNA, can be disruptive to the ion/water complexes that
are complexing with the Z-DNA and maintaining the Z-DNA structure. If the
ion/water complexes are disrupted to the point that they are removed from the
Z-DNA, the Z-DNA converts over to B-DNA and the transcription process (gene set
expression) is started. Similarly, various DNA complexing/coupling proteins may
also be removed from the DNA and gene expression which their presence has been
suppressing will end and transcription will begin. With the proper choice of
microwave frequencies specific sequestered gene sequences can be made to be
expressed at will. Many genetic diseases can be halted, reversed, and or
controlled, fundamental tissue repair can be initiated and the genetic age
clock (telomere length) can be reset to your prime on a regular or periodic
basis.
CONCLUSION:
The normal
aging process where the continuous actions of chemical poisons and microbial
and viral infections take their toll can be halted and reversed. There will no
longer be a falsely fostered need to continually consume some toxic prescription
drugs, which only temporarily mask or alleviate the symptoms of the problem
they are being taken for, while pharmaceutical companies stay on the
prescription drug gravy train. True tissue repair and renewal to the former
state of your prime using energy medicine technologies are now not only
becoming possible, they are becoming available. However, the down sizing of big
pharmaceutical companies and their corrupt influences in regulatory agencies
(FDA, FTC, and U.S. Department of Justice) and legislative bodies must come to
an end for energy medicine technology to be fully developed and implemented
into regular medical practice in your allopathic doctor’s office and your home.
A brave new world of vibrant health stands before you, but you will have to get
off your ass and fight for it with your health dollars, your political voice,
and your social actions. What are you going to do to bring this possible future
to fruition? Not somebody else, but you? Perhaps you can help do in your state
legislature what the citizens of Alberta Province in Canada did in their
legislature. That is they had the following paragraph added to their law books.
“A registered
practitioner shall not be found guilty of unbecoming conduct or be found to be
incapable or unfit to practice medicine or osteopathy 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.“
Is this not a
common sense, honest and intelligent way to practice medicine and give We the
People safe, effective medical treatment options? Now do you not think your
allopathic doctor and or other licensed health practitioner and your friends
and family deserve or have the right to live under such a common sense and just
law? So, what are you going to do about it? Not somebody else, but you. Are you
going to write, call, fax, and make an appointment with your state legislature
representative and express your needs and desires? What are you going to do,
not somebody else? You! Get off your ass!!!
References:
1) Web site
rife.org
2) Web site
rifeenergymedicine.com; read Appendix
A
3) The New
Microscopes, by R. E. Seidel and M. Elizabeth Winter, published both in the
Feb. 1944 issue of The Journal of the Franklin Institute and in the 1944 Annual
Report of the Board of Directors of the Smithsonian Institution.
4) Web site
rifeenergymedicine.com; read A Physicist’s View of
Past Medical Use of Vitamin C and Its Current Active Suppression by Gary
Wade, Physicist.
5) Web site
rifeenergymedicine.com; read Appendix D: The Physical
Structure of Viruses and Bacteria, Which Make Them Extremely Susceptible To
Destruction By Specific Structural Resonant Mechanical Vibrations
6) What Has
Become of the Rife Microscope by Christopher Bird, New Age Journal, March 1976
7) The book: The
Cancer Cure That Worked by Barry Lynes
8) Web site
rifeenergymedicine.com; read the article: Vibratory Energy Medicine by
Gary Wade
9) Web site
rifeenergymedicine.com; read the article: Synergistic Energy Medicine
Therapeutics for use by Alternative Health Practitioners by Gary Wade,
Physicist. Scroll down to pulsed magnetic field section.