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.