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The Theories Behind the Overnight Cure For Cancer
(OCC) by R. Webster Kehr What Causes Cancer? Over the past 100 years
there has been an amazing amount of research implicating a microbe as, not the initial
cause, but as the final cause of cancer. Dr. Royal Rife, whose main
work was done in the 1930s, was not the first person to prove a microbe was
involved in the cause of cancer, but his research was certainly the first to
prove it beyond any reasonable doubt. Rife demonstrated that for
some cases of cancer a virus was the initial cause of cancer because some types of
viruses can, of themselves, penetrate the membranes of normal cells and get
inside the normal cells. But this article will
implicate a microbe as the final cause of cancer in most real-life cases,
not the initial
cause, and will implicate other factors as the reason microbes
can get inside of normal cells. Rife was also the first to
prove beyond any doubt that the microbe involved in cancer was pleomorphic,
meaning the microbe changed forms depending on the terrain it lived in. Pleomorphic means that a virus and bacteria, for example,
may be different forms of the same microbe. This pleomorphic microbe, as
pointed out by Dr. Robert O. Young, PhD, is already in the body of every human
being on earth. It is the "inner
terrain" of the person that allows the microbe to morph into a dangerous
threat to cause cancer. Essentially, every person on
earth has in their body many ultra small microbes that have been called by
different names: "somatid" (per Gaston Naessens) or
"microzyma" (per Antoine Béchamp and the term used by Robert O.
Young) or "bion" (per Wilhelm Reich) or "protit" (per
Gűnther Enderlein). These ultra small
creatures can be thought of as a virus in hibernation. When the inner terrain of
the body changes these ultra small microbes change forms. Gaston Naessens, who, like Royal Rife,
invented a superb microscope, claimed there were 16 different stages these
microbes go through from: virus to yeast to fungal to bacteria and others. While many somatids are
already in the body of every human being, under ideal conditions the microbe is
in hibernation and is not causing any problems.
However, once the microbe, now in a different form because of changes in
the inner terrain, gets inside of a normal cell, there are metabolism changes
that take place inside the cell, leading to the end result of cancer. How this may happen will be described below. There are a wide, wide
variety of factors (such as carcinogens), that allow this microbe, which is already in the
body and is by then in the form of a yeast, fungus, mould or bacteria,
to get inside of a normal cell. Different cancer researchers
have different understandings of this pleomorphic microbe. As a result there have been several different
descriptions of this cancer microbe in the cancer cell. Some people call it a virus, some a fungus,
one called it a mould, others called it an acid-fast bacteria (which mutated
into or from a fungus) or mycobacterium, and one called it an amoeba (e.g.
trichomonad). Which of these is correct? Probably all of them. It should be noted that this
variety of observations is an indication of independent research and that
everyone was not just copying an original source. In fact, there were numerous independent
sources of this information, some dating back to the 19th century!! As mentioned above, this
pleomorphic microbe actually starts out being much smaller than a virus. It exists in everyone's body in a type of
hibernating state until the inner terrain allows it to morph into other
forms. See the absolutely superb book Sick and Tired?, by Dr. Robert O. Young, for a
description of the complete cycle. Dr. Young and Dr. Naessens
are probably the world's foremost experts on this subject. Both have observed this morphing microbe through
live blood microscopes and both have done a great deal of research. While many people scoff at
this concept, it is well known that the "water bear," a very small,
virtually indestructible creature, also morphs and goes into hibernation when
conditions change!! It is in this
hibernation state that the "water bear" is virtually indestructible. How the Microbe Causes
Cancer So how is it possible that a
microbe can be the final cause of cancer? First of all, it is necessary
to understand the "Citric Acid Cycle" or "Krebs
Cycle." This is the cycle that
generates energy for a cell. Another
chain of events is called the Electron Transport Chain (ETC). The ETC is actually an extension of the Krebs
Cycle. Both occur within the
mitochondria in a cell. These two events allow the
ATP inside of the mitochondria to provide the energy to a cell. The question becomes, what
happens if the Krebs Cycle and ETC are broken and do not work and the energy of
a cell drops to virtually nothing? A better question is this:
What can cause the Krebs Cycle and ETC to maintain their broken state? The cell has an amazing ability to restore
the Krebs Cycle and ETC after they are broken. Consider this possible
explanation of why the Krebs Cycle and ETC can remain broken: 1) Due to a weakened,
damaged or incorrectly structured (e.g. incorrectly structured by having
trans-fatty acids being part of the membrane) cell membrane, which can be
caused by a carcinogen or many other things, a microbe already in the body,
which has already morphed into a fungus, mould or bacteria, is able to enter
inside a normal cell, 2) Once inside, the microbe
intercepts the glucose entering the cell (most microbes feed on glucose), 3) The microbe excretes
"mycotoxins," with are highly acidic, and it excretes dangerous
hormones and perhaps a thick slime (mycotoxins are the normal excretions of
microbes), 4) Because mycotoxins are
very, very acidic, the inside of the cell becomes highly acidic, which is a
characteristic of cancer cells, 5) The cell's mitochondria (in
which the Krebs Cycle and ETC perform their functions) get very little glucose (actually
it is pyruvate that gets inside of the mitochondria, but pyruvate is made from
glucose) because the microbe has intercepted most of the glucose, 6) What the cell's
mitochondria do get to "eat" is lots of mycotoxins and other harmful
garbage, which it cannot convert into energy, 7) The mitochondria's energy
level (ATP provides the key energy of a cell, but ATP gets its energy from the
mitochondria) plummets because it is living in a sea of filth, meaning the ATP
energy drops, 8) Signals are sent to the
insulin receptors and glucose receptors on the cell membranes to become
hyperactive and grab more glucose (insulin binds to glucose, thus the insulin
receptors are one way glucose gets inside the cells), 9) More glucose enters the
cell, but most of the glucose is intercepted again by the microbe and the
mitochondria are again bathing in an increasingly large sea of mycotoxins,
dangerous hormones and possibly slime. 10) Because there is a limit
to how high the activity of these two types of receptors can become there is no
way for the mitochondria (and thus the ATP) to get enough glucose and energy, 11) The cell is now
officially cancerous because its energy level drops (the ATP energy levels can
be compared to the steps of a ladder) and the cell is defined to be anaerobic
(i.e. fermenting glucose instead of burning glucose). Several issues have been
ignored, such as how the DNA is mutated (this is covered in the book: Cancer - Cause,
Cure and Cover-up, by Ron Gdanski), to make this simple. The bottom line is that a
"cancer cell" consists of a very, very sick human cell, in which
there is a very, very healthy microbe(s).
Killing this healthy microbe, without killing the sick human cell is a
tricky process. This is why most
alternative cancer treatments kill the cancer cell, even if they are oxygen
based. Ozone, for example, is the most
alkaline substance on earth, but it kills the cancer cells. There is one more
interesting thing about this process. Dr.
Otto Heinrich Warburg, a two-time Nobel Prize winner, is the person who discovered
that cancer cells get energy by fermenting glucose. In his own words, Dr. Warburg
said the following: "But, even for cancer there is only one primary
cause. Summarized in a few words, the cause of cancer is the replacement of the
respiration of oxygen in normal body cells by a fermentation of sugar [glucose]." Otto
Warburg, The Prime Cause and Prevention of Cancer, 1966, pg.6. Why is that important? Without going into a lot of detail, fermentation is
impossible without yeast!!
So how does yeast get inside a cancer cell? Again, to make a long story short: the yeast
form is one of the forms of the pleomorphic microbe!!! The microbe may enter the cell as a fungus, mould
or bacteria, but once inside the cell it apparently can perform the duties of a
yeast (i.e. fermentation). Whether it
morphs into a yeast inside the cell, or simply performs the duties of a yeast,
is not known. Here is a relevant quote: "The medical fields of mycology (the study of
fungi) and oncology (the study of cancer) may seem to be independent
fields. Fungi are ubiquitous; yeast is
required for fermentation. Nineteenth
century researchers began to use the terms "cancer,"
"fermentation," and "tubercles"[i.e. tuberculosis, which is
generally caused by a virus or bacteria] interchangeably... Although we
understand that the fermentation process requires yeast, we scoff at the role
of fermentation in cancer research." The Germ That Causes Cancer, by Doug A. Kaufmann, page 30 It should be noted that the
acid-fast bacteria and the mycobacteria mentioned above look so much like
fungus that some researchers have called them a fungus and others a bacteria. It is well known and well documented that
some fungi infections were actually misdiagnosed as leukemia. Indeed, this
pleomorphic microbe is so highly involved in the formation of cancer that it is
sometimes misdiagnosed as cancer. Some
lumps, which are diagnosed as tumors, are actually a fungal growth. How do DMSO and MSM
work? DMSO and MSM are the two key
ingredients in the OCC. First, it should be clearly
understood that DMSO targets cancer cells and gets inside of
cancer cells. In this classic study: "Haematoxylon [a dye] Dissolved in
Dimethylsulfoxide [DMSO] Used in Recurrent Neoplasms [i.e. cancer cells or
tumor cells]," by E. J. Tucker, M.D., F.A.C.S., and A.
Carrizo, M.D. in International Surgery, June 1968, Vol 49, No. 6, page 516, it was shown that DMSO bound
to the dye (i.e. haematoxylon) and targeted cancer cells. Some of the cancer patients were cured during
this study, even though DMSO was only being combined with a dye!! Here is an online copy of
this classic article: http://www.cancertutor.com/Dmso/DmsoArticle.html DMSO has also been shown to
bind to several kinds of chemotherapy and still be able to target cancer
cells. See the book: Treating Cancer With Insulin Potentiation
Therapy, by Ross A. Hauser, M.D.
and Marion A. Hauser, M.S., R.D.
(chapter 22, and others) No one knows for sure how DMSO
and MSM work, but it is clear that the DMSO gets inside of the cancer cells. Perhaps once inside of the cancer cell the
DMSO molecules release their extra oxygen atoms, and these oxygen atoms kill
the microbes inside the cancer cells without actually killing the cancer cell
itself. No microbe has ever developed an immunity
to oxygen! It should be emphasized that
there is a vast difference between an oxygen pair (O2) versus an
oxygen singlet (O1). Most of
the oxygen in the body is the very stable oxygen pair. But there is a great need in the body for
oxygen singlets, such as to kill microbes or neutralize a number of dangerous
molecules (see the book: Flood Your Body With Oxygen, by Ed McCabe). Most people have a
significant shortage of oxygen singlets due to the way food is processed. Both DMSO and MSM, among other things,
provide oxygen singlets, without providing a high amount of alkalinity, which
is why they can be taken in such high doses. DMSO is not alkaline and
cannot kill a cancer cell. Neither can
MSM. However, DMSO can "carry"
other molecules (by binding to them) inside of cancer cells which do kill the
cancer cell. Once the microbe(s) inside
the cancer cells are killed, without the cancer cell itself being killed, the
cell can start the process of returning to normal because the mitochondria will
now get the glucose that is entering the cell. This death of the microbes can occur
overnight, but the process of the cell changing metabolism may take the cell
several days or several weeks. Thus, do
not expect to see the results of the Overnight Cure for Cancer (OCC) overnight. It is actually not known how long it will
take for the metabolism to change back to normal. The trick to reverting
cancer cells into normal cells is hopefully as simple as killing the microbe(s)
which are inside the cancer cells, without killing the cancer cell itself!! In fact, Royal Rife proved
that by killing the microbe inside the cancer cell (he used electromagnetic
waves that were based on the resonant frequency of the microbe), or by damaging
the microbe so that it cannot reproduce, the cell will revert to normal and the
cell will eventually die a normal death. DMSO has been proven in vitro (in glass) to revert cancer
cells into normal cells. More than a dozen natural
substances are known to revert cancer cells into normal cells. DMSO is one of them. More research has been done on DMSO, on more
lines of cancer, than any other substance.
See the book: Cancer & Natural Medicine, by John Boik
(pages 9-11) DMSO is able to revert
cancer cells into normal cells in vitro,
and it may be because of its ability to release oxygen singlets after it gets inside
of cancer cells. There are several other
theories as to how DMSO is able to differentiate a cancer cell (i.e. revert a
cancer cell to a normal cell). Substances which can revert
cancer cells into normal cells used to be called "polar solvents" in
the medical literature. It should also be noted that
neither DMSO nor MSM are strong enough to kill a cell, whether cancerous or
non-cancerous. Oxygen singlets and
sulfur do not kill cells, but oxygen singlets can kill microbes. Thus, it is almost impossible for this
treatment to kill any cancer cells. The
goal of the OCC is to revert as many cancer cells into normal cells as
possible, and kill as few cells as possible. However, in order for DMSO to
maximize its effectiveness, it is necessary to combine DMSO with retinoic acid
(see the Boik book). But in order for
retinoic acid to be effective it is also necessary to add Vitamin C. When these two items are added to the OCC,
however, many cancer cells are killed, that is why they are no longer part of
the OCC. In addition, there are some
who believe the combination of glucose (e.g. fructose) and DMSO kills cancer
cells. Since the liver constantly
creates glucose from lactic acid, it is impossible to completely remove glucose
from the body during the OCC. Thus, if
this theory is true, there may be some cancer cells die due to the glucose in
the body. Whether any cancer cells are
killed during the OCC is not known, but at the current time the OCC includes a
buildup period where, if significant problems do occur because of the killing
of cancer cells, this should be realized while the doses are still low. In other words, the buildup may provide an
early warning system. The theory of oxygen singlets
from the DMSO (as the theory of why DMSO is able to differentiate cancer cells),
is consistent with all of the theories of why cancer forms in the first place,
to why the OCC might revert cancer cells into normal cells. It explains these things in a logical
sequence based on a great deal of known scientific facts and a little common
sense. Such a treatment could be
used like aspirin. If you got a
headache, you would take aspirin. If you
got cancer, you would take a week off of work and cure your cancer at home. That is what the OCC is all
about. How To Cure Cancer
Quickly The reader might have
wondered why the OCC does not want to kill any cancer cells. This section will explain why. There are about a dozen
alternative cancer treatments that currently have about a 50% cure rate on
advanced cancer patients (e.g. those sent home to die by orthodox medicine). Every one of these
treatments works by killing cancer cells. Because these treatments
kill cancer cells, they cannot work too quickly. Most of these treatments take at least two
months or more to cure cancer (i.e. kill virtually all of the cancer cells). The reason these treatments
take so long to work, in spite of the fact that they target cancer cells and
safely kill them, is because as a cancer cell is dying, it gets
"sick" and the immune system attacks it, causing potentially
dangerous swelling and inflammation. In other words, the reason
these treatments cannot be done overnight and must be done over months of time
is because of two reasons: 1) When cancer cells die the
body needs time to remove it. When many
cancer cells die at the same time, the body can be overwhelmed with the task of
removing all of the dead cancer cells (i.e. debris) safely. Thus, there is a limit to how many cancer
cells can be safely killed at the same time. 2) As the cancer cells are
dying, the immune system can create swelling and inflammation as it attacks
them, which can be dangerous for certain kinds of cancer, especially brain
cancer, lung cancer, and cancers of the digestive tract. However, when a treatment is
developed that reverts cancer cells into normal cells, there are no huge
amounts of dead cancer cells the body needs to get rid of - hopefully. Nor is there any swelling and inflammation to
worry about. Thus, if someone wanted to develop a
cancer treatment that could work fast, it would have to be a treatment that
reverted cancer cells into normal cells!! The Four Theories Behind
the OCC The OCC treatment can be simplified
to this: a person consumes exact amounts of DMSO and MSM every half-hour for 12
hours (the "exact amount" will vary from person to person). However, the person does not
eat for the 12 hours before the treatment begins, then the person
is on the treatment for 12 hours (when the DMSO and MSM are consumed), then the
person still does not eat anything for an additional 12 hours after the treatment. Thus the complete OCC lasts for a total of 36
hours without eating. With this big picture in
mind, here are the four theories behind the simple treatment. Theory #1 – Reverting
Cancer Cells into Normal Cells This was discussed
above. The key point to remember from
above is that the only possible way to cure cancer quickly is to use a
treatment that very efficiently converts cancer cells into normal cells,
meaning only a low percentage of the cancer cells would be killed during the
treatment. Theory #2 – The “Juice
Fast” This treatment actually does
not
allow fruit juice during the treatment, however, it follows the same theory as
a “juice fast.” The basic concept of a
“juice fast” is that the body has nothing to eat or drink except what you give
it. Thus, if you smoke, drink alcohol,
eat sugar, eat refined flour, etc., and nothing else, you may not get the
nutrients you need to keep your immune system strong because the things you
take into your body are the only things your body has to work with. On the other hand, if the
only food you ate was grapes (i.e. the Brandt Grape Cure of the 1920s), for
example, then your body (i.e. your cancer cells) would have nothing to eat
except grapes. In the Brant Grape Cure
the cancer patient (i.e. the cancer cells) has nothing to eat except
grapes for up to several weeks. It is a
very, very effective cancer treatment. There are several well known
"juice fast" based alternative cancer treatments, such as: 1) The Brandt Grape Cure,
where the person is not allowed to eat anything except red, purple or black
grapes for 2-5 weeks at a time, 2) The Brand Grape Cure
using carrot juice and beet juice (and perhaps other vegetable juices) instead
of the grapes, 3) The Breuss Total Cancer
Treatment, in which a person is not allowed to eat anything but a low-glucose
herbal tea for 42 straight days. With the OCC treatment, the cancer cells
have absolutely nothing to "eat" for the 36 hours of the treatment - except
for DMSO and MSM!!. Even during the 12
hours before the treatment begins, the cancer cells are starting to get
“hungry,” and are "waiting" for something to eat. Since DMSO targets cancer
cells, the hungry cancer cells get an abnormally high dose of DMSO and MSM - and nothing
else!! These are
important concepts!! Theory #3 – The Colon
Cleanse The important issue with
“juice fasts” is that the body has absolutely nothing to eat but what you feed
it. But what about the decaying food in
the colon at the beginning of the treatment?
Aren’t the nutrients and other things in the colon slowly released
during a "juice fast" type of treatment, thus competing with, and diluting, the
effectiveness of the treatment?
The answer is ‘yes’. It just so happens that in
the Brandt Grape Cure, the first several days of the Brandt Grape Cure actually
accomplishes a very effective detoxification and colon cleanse. After the colon is cleansed by
eating/drinking nothing but pure grape juice for the first few days of the
treatment, the body truly has nothing to eat except grapes. Since grapes contain more than a dozen
nutrients that kill cancer cells, it is a very potent cancer treatment. The OCC is very similar to
the Brandt Grape Cure in the sense that the colon should be cleaned out. However, this treatment does not last long
enough to cleanse the colon by itself.
Nor is the OCC itself designed to do that. Thus, an outside means is needed - before the
treatment begins. When the treatment begins,
the colon should have been cleaned out at least 12 hours earlier. The full effectiveness of the treatment can
only occur after the colon is cleaned out.
Until then, the clogged colon is pushing things into the blood stream
that may interfere with the treatment. Theory #4 – Consuming
Small Quantities of Something Many Times The fourth key concept of
this cancer treatment is that if you eat small quantities of something, many
times, over the period of several hours, the body will assimilate a higher
percentage of the nutrients than if only one or two large doses were taken. In other words, the digestive system, body
and cells can process a higher percentage of the substances if it is given more
time by a large number of spread-out small doses. For example, suppose you
learned that the combination of DMSO and MSM reverted cancer cells into normal
cells (which they do in vitro). Suppose you weighed 200 pounds and you
calculated you could safely consume 25 tablespoons of DMSO and 25 grams of MSM total
in one day. Which would be more
effective, taking all of the products at one time, or taking 1 tablespoon of
DMSO and 1 gram of MSM, each half hour, for twelve hours (the 25th dose is at the end of
the last hour)? The answer is that the body
would absorb and assimilate and benefit much more from taking the DMSO and MSM
spread out over 12 hours (1/2 hour apart), than by taking the products all at
once. Large doses of a substance
pass through the body very quickly and much of the substance is not absorbed by
the body. An I.V. is essentially
another example of this concept. Rather
than give a person a large dose of something at one sitting, the dosage is
spread out very slowly over several hours so more of it is absorbed and assimilated
by the body. This treatment is actually a
modified I.V. because it uses many small doses spread out over 12 hours (i.e.
25 doses taken over a twelve hour period). A Summary of the
Theories Behind the OCC Here is a summary of some of
the secrets of Mother Nature that the OCC takes advantage of: 1) The OCC uses known ways to revert cancer cells into
normal cells by changing the metabolism of the cancer cells into the metabolism
of normal cells (e.g. probably by killing the microbe inside the cancer cells). 2) During the treatment the body (i.e. the cancer cells)
will have zero glucose to eat (except for the glucose created by the liver from
lactic acid), meaning the insides of the cancer cells will basically get only
DMSO and MSM, meaning extra oxygen and sulfur atoms. MSM may bind to the lactic acid, and remove
it from the body, thus reducing the amount of glucose in the body (cancer cells
convert glucose into lactic acid, the liver then converts the lactic acid back
into glucose, creating the "lactic acid cycle" or "cachexia
cycle"). 3) The only way to cure cancer quickly is by reverting
cancer cells into normal cells. 4) When reverting cancer cells into normal cells,
hopefully few cancer cells are killed (with a resultant small release of
toxins), thus this treatment can be done quickly because the treatment itself
is not toxic. 5) The concept of a “juice fast” results from the
concept that the body (i.e. the cancer cells) has absolutely nothing to
“eat” except what you give it. 6) A colon cleanse is important to minimize the amount
of food-stuff competing with the treatment plan. 7) The body will absorb and utilize far more of
substances if they are given in small doses over time as opposed to a few large
doses. The “Cure Rate” For This
Treatment Let us, for the sake of
argument, assume that this “Overnight Cure for Cancer” actually converts every
single cancer cell in a person’s body into being a normal cell. At some future time it may evolve into a
treatment that does just that. If this were a true
statement for every patient, most people would assume that every person who
takes this treatment would survive their cancer and live to a ripe old age. In other words, they would assume it would
have a 100% true cure rate.
Unfortunately, it is not as simple as that. Cancer patients generally go
with orthodox medicine first for treatment.
Orthodox treatments rarely work and eventually almost all cancer
patients are sent home to die. When they are sent home to
die they are in critical condition with many severe health problems, including
a damaged heart, an immune system which has been destroyed, a damaged stomach
lining, etc., etc. The best of the strongest alternative
cancer treatments only have a 50% true cure rate on cancer patients sent home
to die. As mentioned above, there are very few of the
alternative cancer treatments that can achieve that cure rate. Half of the cancer patients
have simply had too much damage done by orthodox medicine, and have lost too
much treatment time, to survive the 3-6 months of treatment using current
techniques (the treatments are longer for some types of cancer). The bottom line is that by
the time orthodox medicine sends a person home to die, even if every cancer
cell in their body was suddenly converted to being a normal cell, the person
may still die. They might die from damage
to a major organ which occurred prior to the natural treatment, or they might
die from malnutrition which started prior to the natural treatment, or they
might die from the side-effects of toxicity caused by chemotherapy or radiation
before the person was sent home to die, or they might die from damage to the
heart caused by the orthodox treatment, or from any of a number of other causes
which are delayed reactions to the orthodox treatments. In other words, even if this
treatment were totally non-toxic (which it is), many cancer patients will still
die from an irreversible delayed reaction resulting from their prior orthodox
cancer treatment, even if every cancer cell in their body were reverted into a
normal cell within 24 hours. The OCC is currently not a
treatment for cancer. It is only
currently designed to assist the "Stage IV" treatments. But even if the current version of the OCC
only reverts 25% of the cancer cells into normal cells (the actual percentage
may be higher or lower than 25%), that is 25% less inflammation, 25% less
swelling and 25% less debris from dead cancer cells to deal with. But even if the day comes
that it becomes a stand-alone "Stage IV" treatment, it will never
achieve a 100% cure rate for people sent home to die by orthodox medicine. The best it could ever theoretically achieve
would probably be in the 60% range. For those who go with
alternative medicine first, however, and totally avoid orthodox medicine, this
treatment could some day achieve a true cure rate of over 99%, especially when
given as a complete protocol with other substances. There are a few rare types of cancer, such as
Russell's Syndrome, which involve more than just cancer cells, thus a 100% true
cure rate is many years away. One Final Comment About
Theory As this is being written,
the OCC is the only cancer treatment in the world that has a good chance of
reverting cancer cells into normal cells. However, back in the 1930s
there was a treatment that was very successful at reverting cancer cells into
normal cells. That treatment was the
product of Dr. Royal Rife. Dr. Rife used an
electromagnetic machine to kill the microbes which were inside of the cancer
cells. At the current time there is
no "Rife Machine" (may people use the term "Frequency
Generator" to avoid government persecution) that is able to do this. His techniques and frequencies were lost to
the world as a result of the persecution, greed and corruption, not of Royal
Rife himself, but of others. However, there is almost a
cult following of Royal Rife today and many people are studying and researching
what Royal Rife did. When the day comes that the
frequencies are again known to the world and made public, using the Rife
treatment after
the OCC would be a superb thing to do. The reason these two
treatments should be back-to-back is that the OCC will, as a minimum, weaken
the microbes inside the cancer cells.
These weak microbes will be even easier to kill by a Rife Machine than
healthy and "well fed" microbes. The reason can be understood
by thinking about a chiropractor. A
chiropractor can much more easily manipulate a small, skinny person than a
large, overweight person. A frequency generator works
by vibrating or oscillating the microbe (i.e. resonant frequencies). The oscillation will be much more effective
if the microbe inside the cancer cells is starving for glucose, rather than
"full" of glucose. Thus, preceding a Rife
treatment, should the day ever come that the secrets of Rife are again
discovered, by the OCC, would be a superb combination. |