You would not believe how many emails we have gotten from cancer patients who have gone through these three steps:
- The patient had chemotherapy, radiation, and surgery to treat their cancer;
- The patient was told they were “cancer-free”;
- Months later cancer “came back,” which is called “regression.”
Among other things, this article will explain what went wrong and how to prevent cancer from coming back. When talking about what causes cancer we need to talk about it at two different levels.
The first level is talking about cancer at the systemic level, meaning what conditions in the body allowed cancer to grow out of control and how do we deal with this issue.
The second level of talking about cancer is talking about what causes cancer at the cellular level. In other words, why does a healthy cell become cancerous?
As part of this, we will also discuss how to revert cancer cells into normal cells, which is one way to treat cancer. For example, the Dirt Cheap Protocol has more than a dozen treatments that revert cancer cells into normal cells.
These two subjects are totally different!
We can compare these two levels by talking about a flood. We could talk all day long about the damage a rain storm caused, such as the flooding of rivers, the damage to crops caused by heavy rain, the damage to roads that have flooded, etc.
But that is only one level to talk about. We could also ask what weather conditions caused rain to form in the clouds. Thus, a scientist might talk about what causes rain up in the clouds, but a newscaster might talk about the damage caused by the flooding of a river caused by the rain.
The same is true about cancer. A cancer practitioner might research how to kill cancer cells or revert them into normal cells, but a cancer researcher might ask why the immune system was weak and why individual cells were cancerous.
A discussion about what causes cancer at the cellular level is a totally different subject than talking about what causes cancer at the systemic level.
Five ways to ‘cure' cancer
3. Supercharge the immune system to create interleukin and interferon and other neuropeptides, which in turn kill the cancer cells.
4. Kill the parasites and microbes in the organs, which will also help supercharge the immune system.
5. Supercharge the immune system with nutrients (though it does not work as fast as some of the other treatments).
Fixing the root cause of cancer
While many natural cancer treatments do very well against cancer, what is missing in many natural cancer treatment protocols is getting rid of the microbes in the organs, which is the root cause of most cancer.
In many cases, the immune system can get rid of these microbes, but in fact, some types of tapeworms, flukes, and fungus, etc. cannot be killed by the immune system for one reason or another (e.g. the microbes are not accessible by the immune system).
Liver flushes and special nutrients may be required to deal with these microbes and parasites. But the fact is that many natural cancer treatments do very well without dealing with these special microbes. But the patient should be aware of these issues.
By getting rid of the microbes in the organs, plus doing the normal cancer treatments, the balance (i.e. a strong immune system and a low number of cancer cells) is restored enough to keep cancer from coming back. The patient is cured because their immune system has been fixed and the number of cancer cells (by using special protocols) has been reduced. Cancer will not come back as long as the patient watches their diet.
The approach of orthodox medicine, however, is to severely damage the immune system with chemotherapy, radiation, and surgery. This makes the imbalance even worse because these things damage the immune system and do a very poor job of targeting the cancer cells and do an even worse job of killing the microbes in the organs.
Orthodox cancer treatments also kill many healthy cells and can damage organs, the lymph system, etc. Is it any wonder cancer always seems to “come back” after surgery or chemotherapy? This is called “regression.”
For example, how does cutting off a breast going to fix the immune system? Don't be absurd. I don't know how many times I have told cancer patients that “you cannot cut cancer out.”
Is it any wonder that alternative cancer treatments, when administered by experts, have a massively higher cure rate than orthodox medicine? Most natural cancer treatments include immune builders and things that kill cancer cells. Some protocols also include things to clean the blood of microbes, which also will supercharge the immune system.
Ponder this carefully: Even when orthodox medicine puts someone into “remission” (i.e. their cancer appears to be gone), they have not fixed the root cause of cancer, so it is almost certain cancer will come back.
Because the root cause of cancer is a weak immune system, you cannot cut cancer out. You have to deal with the root cause of cancer.
“A discussion about what causes cancer at the cellular level is a totally different subject than talking about what causes cancer at the systemic level.”
The Cancer Tutor
Cancer on the systemic level
Everyone has cancer cells in their body, so why does one person never get diagnosed with cancer and another person is diagnosed with cancer? Cancer is almost always caused by the same multi-step sequence of events.
First, nasty microbes and parasites get inside of the organs and make their homes there. These microbes generally come from meat that was not adequately cooked, but they can come from other sources.
Second, these microbes intercept glucose which was headed for the cells in the organs.
Third, these microbes excrete (as waste products) mycotoxins, which are highly acid and totally worthless to the cells.
Fourth, because the cells (in the organs) don't get the food they need (because it has been intercepted), and because they are living in a sea of filth (i.e. mycotoxins), the cells in the organ become weak.
Fifth, organs are made exclusively of cells. In other words, if you took all of the cells out of an organ, there would be no organ. Thus, because the cells in the organ(s) are weak, the organ(s) are weak.
Sixth, because one or more major organs are weak the immune system becomes weak. Actually, the microbes weaken the immune system both directly and indirectly.
Seventh, because the immune system is weak it cannot kill enough cancer cells and the cancer cells grow out of control.
Thus, in summary, the root cause of cancer is microbes and parasites that are in the organs or colon (or bloodstream), which weakens the immune system.
However, other things can cause cancer. For example, a vaccination can weaken the immune system due to mercury and / or toxins. Filth in the colon can also lead to a weak immune system (see the book: Fire in the Belly by Dr. Keith Scott-Mumby)
The reader might have noted the “or bloodstream” above. Cancer patients who have microbes in the organs also have microbes in the bloodstream. Which caused the other will vary by the cancer patient. But microbes that originate in the organs will spread microbes to the bloodstream, and vice versa. Exactly how much the microbes in the organs weaken the immune system, versus how much the microbes in the bloodstream weaken the immune system varies by case, but parasites likely would be found in the organs.
When thinking about the above steps, there are three major ways to cure cancer:
- Safely target and kill the cancer cells;
- Kill the microbes inside the cancer cells (which will be discussed below) and the cancer cells will revert into normal cells;
- Kill the microbes that are causing the immune system to be weak (and this includes the microbes in the organs and the microbes in the bloodstream).
Actually, without doing No. 3, cancer could come back again.
The reader might wonder if there are any natural cancer treatments that are specifically designed to identify and get rid of the microbes in the organs? The answer is yes.
For example, the High RF Frequency Generator with Plasma Amplifier or High RF Frequency Generator with Linear Amplifier will kill these microbes and parasites without knowing what they are. This is because this device will cover enough frequencies to kill all of these microbes and parasites.
Another option is “liver flushes,” such as designed by Hulda Clark or Ty Bollinger (in his book The 31-Day Home Cancer Cure).
So in short, there are treatments for all budgets.
The definition of cancer cells
So what causes an individual cell to become cancerous? Many cancer cells form by a prior cancer cell dividing and creating two cancer cells. But how does a normal cell, which is not cancerous, become cancerous?
In a normal cell, molecules called ATP (adenosine triphosphate) provide the energy of the cell. ATP molecules are created inside the mitochondria which are inside of every human cell. In fact, there are thousands of mitochondria inside of every human cell.
The very definition of cancer cells is low ATP energy.
The normal process of creating ATP molecules is this (highly simplified):
- Glucose gets inside of the cell from the bloodstream;
- Some of the glucose is converted into pyruvate (this is a multi-step process);
- Pyruvate gets inside of the mitochondria;
- Once inside the mitochondria, pyruvate is at the beginning of two sequential chemical reactions (the Citric Acid Cycle or Krebs Cycle and then the Electron Transport Chain which spins off about half-way through the Citric Acid Cycle). It is these two cycles which create most of the ATP molecules in the cell.
Cancer cells consume 15 times more glucose than a normal cell. Thus, a person would logically expect a cancer cell to create 15 times more ATP molecules than a normal cell.
But in reality, cancer cells create a very small number of ATP molecules. Cancer cells are ATP molecule-starved and they have to revert to fermentation to create what little ATP molecules they create.
With so much glucose there should be an abundance of ATP molecules. Why do cancer cells consume 15 times more glucose and yet not be able to create a significant amount of ATP molecules?
The thing that blocks the production of ATP molecules is a very special pleomorphic bacteria that is inside the cancer cells.
The Independent Cancer Research Foundation and others believe the microbe is Helicobacter Pylori or H. pylori. In some cases, Fusobacterium may be involved as well as it is also known to get inside of cells.
While everyone has H. pylori bacteria in their body (generally in their digestive tract), how do H. pylori get inside of a healthy cell? Generally, it doesn't. But in some cases, an acidic diet can make this bacteria highly aggressive and it can literally drill itself inside of a normal cell to get away from the acidity in the blood, as discovered by Robert O. Young, Ph.D.
Another way microbes can get inside of cells is because asbestos or the chemicals in tobacco cut the cell membrane. This can allow microbes inside the cells. But remember that even though all of us have cancer cells, don't forget we also have an immune system.
So how does a bacteria block the production of ATP molecules and thus turn a cell cancerous after it has gotten inside the cell?
In 2004, the Independent Cancer Research Foundation developed the model which still stands today.
The bacteria blocks ATP production in two different ways:
First, bacteria eat glucose so as the bacteria proliferate inside the cell (by the way, a bacteria is roughly the same size as mitochondria) they intercept more and more glucose. This means less and less pyruvate is made because there is less glucose to be converted into pyruvate. This means less ATP is made.
Second, microbes excrete mycotoxins, which are highly acidic and totally worthless molecules.
As one ICRF researcher put it: The mitochondria, instead of “swimming” in a sea of pyruvate are swimming in a sea of mycotoxins.
Both items contribute to the mitochondria not obtaining enough pyruvate and this hinders both the Citric Acid Cycle and the Electron Transport Chain and thus blocks the production of an adequate amount of ATP in the mitochondria.
This microbe is highly pleomorphic, meaning it has many different sizes and shapes. This microbe can literally be smaller than a virus. Many people think it is a virus or fungus that causes cancer, but it is actually a cell wall deficient highly pleomorphic bacteria.
In one of its smaller states, it is the size of a virus and can enter inside of the cell nucleus. Like a virus, which gets inside of the nucleus, the DNA of the cancer microbe can interact with the DNA inside the cell nucleus and change the DNA structure of the cell.
- More importantly, the Dillers [who were part of the Dr. Virginia Livingston team] showed that cancer germs [i.e. microbes] were able to gain entrance not only into the [non-cancerous] cell (intra-cellular), but also into the nucleus of the cell. This intra-nuclear invasion meant that cancer microbes could gain access to the genes contained within the nucleus itself. — Four Women Against Cancer, by Dr. Alan Cantwell, page 47
Scientists see the DNA damage caused by these microbes and claim that it is DNA damage which causes cancer. This is like saying that smoke is the cause of fires. It is a good guess, but it is false. The DNA damage of a cancer cell is caused by the DNA of the same highly pleomorphic bacteria that blocks the production of ATP molecules. Actually, this bacteria does many other things to create cancer cells, protect cancer cells from the immune system and spread cancer. In fact, the characteristics of this bacteria are mind-numbing.
Thus, the claim by cancer researchers (who are funded by the pharmaceutical industry) that DNA damage causes cancer is wrong. Whether this is an intentional error (i.e. to avoid finding a cure for cancer) or is caused by ignorance I do not know.
In any case, due to the lack of energy in cancer cells (i.e. due to the lack of ATP molecules), cancer cells are very weak, which is the definition of a cancer cell. But because cancer cells steal glucose from the body the non-cancerous cells have less glucose and are very sick. They are sick for other reasons as well (e.g. cachexia cycle as cancer cells excrete lactic acid).
Many cancer researchers, starting over 100 years ago in the 1890s, have isolated the cause of cancer to be microbes (at the cellular level), though they did not understand the mechanism inside the cell which caused a microbe to make a cell cancerous.
- In 1890 the distinguished pathologist William Russell (1852-1940) first reported “cancer parasites” in cancer tissue that was specially stained with carbol fuchsin, a red dye. The “parasite” was found inside and outside the cells. The smallest forms were barely visible microscopically, and the largest parasites were as large as red blood cells. Russell also found “parasites” in tuberculosis, syphilis and skin ulcers. — Four Women Against Cancer, by Dr. Alan Cantwell, pages 53-54
Dr. Russell, in 1890, knew that the cancer microbes were pleomorphic.
Note that the cancer microbe was found both inside and outside of the cancer cells. One method that cancer cells use to spread quickly (at least for some kinds of cancer) is for the cancer microbe to come out of the cell, travel through the blood and create a new “colony” of cancer cells far from the original colony. Squamous Cell Carcinoma, melanomas, sarcomas and uterine cancer have all been identified by ICRF researchers as spreading in this way.
This is just the beginning.
The cancer microbe also excretes enzymes that coat the outside of the cancer cells. This coating of enzymes blocks the immune system from identifying the cancer cells as being cancer cells.
It was also discovered, around the 1950s, that natural pancreatic enzymes, made in the pancreas, could dissolve this protein coating so the immune system could identify and thus kill the cancer cells.
This discovery, in turn, led to the advice that natural cancer treatments should prohibit the cancer patient from eating meats or other foods that the pancreatic enzymes cut apart. In other words, these foods “use up” the pancreatic enzymes while in the stomach so less of them are available to expose cancer cells to the immune system.
When a cancer patient is using pancreatic enzymes in their protocol, they should not eat meat or dairy products. In fact, no cancer patient should eat very much meat and they should not eat or drink any dairy products (for multiple reasons) or sugar.
The trade off is that meat can help a weak cancer patient who is not on a pancreatic enzyme protocol so in some cases meat is fine for a cancer patient.
Dr. Matthias Rath discovered that these microbes excrete enzymes that cut a path along tissue so cancer can spread more easily along the tissue. The cancer microbes are a cancer-causing machine.
In summary, cancer at the systemic level is caused by an imbalance between the strength of the immune system and the number of cancer cells. At the systemic level many, many things can cause cancer, especially things that weaken the immune system. The weak immune system is almost always caused by microbes and parasites which are inside the organs but are not necessarily inside the cancer cells.
But cancer at the cellular level is caused by very unique and common microbes which are inside of the cancer cells. These microbes do many amazing things to help cancer cells do their damage and protect themselves.
Cancer cells create and excrete large amounts of lactic acid, as already mentioned, as they process large amounts of glucose inefficiently. This lactic acid goes into the bloodstream and gets to the liver. The liver converts the lactic acid to glucose. This “ping pong ball” cycle, where the cancer cells convert glucose into lactic acid and the liver converts lactic acid into glucose, is called the lactic acid cycle or cachexia cycle.
This cycle is what kills about half of all cancer patients because so much energy is consumed at both ends of the cycle. The patient becomes weak and simply dies.
The lactic acid also blocks many key nutrients from getting to the cancer cells.
Dealing with the lactic-acid cycle is frequently a major effort of a cancer treatment. It may involve using hydrazine sulfate, Methyl-Sulphonal-Methane (which helps flush out the lactic acid), D-Ribose (to get the energy to the non-cancerous cells), Vitamin C (ditto), etc. etc.
Here is an article which shows the 16 different names of the different sizes of the cancer microbe (the images are not to scale or shape): Advanced Cancer Theory
Cancer is not caused by DNA damage
Microbes can lower ATP energy, which is the very definition of a cancer cell. Are there other things that can lower ATP energy? In theory, there are, but from a statistical standpoint, any other cause would be almost statistically impossible.
One possibility is DNA damage where the DNA damage causes defective proteins and the defective proteins cause a loss of some ATP energy.
As I will point out, it is doubtful that more than a few thousand cancer patients worldwide, if any, have cancer caused by DNA damage.
But it is almost certain that certain chemicals, especially asbestos, can cause cancer. It is almost certain that asbestos causes cancer by cutting the sides of cells, thus allowing bacteria to get inside the cancer cells more readily. And it is then the bacteria that causes cancer as we have already seen.
Let's talk more about the possibility of DNA damage causing cancer.
Orthodox medicine claims that all cancer is caused by DNA damage. This is nonsense. However, in theory in rare cases, DNA damage may cause cancer.
Let's talk about the famous BRCA2 gene as an example. Can a defect in this gene cause cancer? It is not clear whether the BRCA2 gene is a cause of cancer or that the microbes inside the cancer cells cause the BRCA2 gene damage. Orthodox medicine would never examine this issue because they are looking to sell drugs, not save lives.
A DNA strand is between 3.2 billion and 3.5 billion nucleotides long. Only a very small percentage of this DNA codes for proteins, about 3 percent. And only a very small percentage of these proteins are involved in the creation of ATP energy. The proteins we are interested in are the proteins needed for the conversion of glucose to pyruvate, for example.
In other words, we are only interested in the structures inside the cells which are involved in the conversion of glucose to pyruvate.
It is possible, but highly unlikely, that DNA damage could affect one of the proteins needed for the creation of ATP energy.
As the cell with this DNA damage divides, all of the “daughter” cells” will have this same genetic damage.
So how does a bad gene create a cancer cell? In a cell, genes are the patterns used to make enzymes or proteins. If a gene is damaged then the enzymes or proteins made by this gene will be defective.
Everything that goes on in a cell is controlled by proteins. There are worker proteins, supervisor proteins, etc. If these are damaged then one or more of a large number of chemical chain reactions inside the cell may fail. This may mean the creation of ATP is damaged.
If a significant amount of ATP energy production is blocked inside the cell, then by definition the cell is cancerous.
So how exactly could the BRCA1 or BRCA2 defective genes cause cancer? The truth is that no one really knows whether these defective genes cause cancer at all. In order for these defects to cause cancer, they must create defective proteins that are needed for the conversion of glucose to pyruvate.
A genetic defect may have absolutely nothing to do with the creation of pyruvate. In other words, genetic defects may be a symptom of cancer, meaning this damage may be caused by the DNA of the microbes which are actually causing cancer.
These defects cannot block the ATP production completely or the cell would fall apart. So we do know it must be a partial interference if at all.
For now, we will have to say, “We don't know if the defective genes are a cause of cancer or a symptom of the presence of the microbes that cause cancer.”
Focusing on microbes inside cancer cells
Let's ask one more question: Have there been any cancer treatments that cured cancer by killing the microbes inside the cancer cells?
In the 1930s Dr. Royal Rife, a microbiologist, was able to cure cancer with gentle electromedicine, which had two frequencies. One frequency was designed to kill the cancer bacteria and the second frequency was a “carrier” frequency which got the other frequency through the cell membrane (and actually through the entire body) to get inside the cancer cells to kill the microbes.
Dr. Rife had a 100 percent cure rate of cancer patients, but he was shut down by the FDA after refusing to sell his technology to the American Medical Association, which he knew would bury his technology.
Two modern-day Rife machines have replicated both of the types of machines that Rife built. These are the High RF Frequency Generator family of gentle electromedicine devices.
The Independent Cancer Research Foundation researches both electromedicine protocols (such as Rife developed) and has also designed several cancer treatments using: DMSO, MSM, honey, maple syrup or molasses as carriers (i.e. Trojan Horses) to get microbe-killing substances inside of cancer cells. These treatments have been very successful.
In other words, if you kill the microbes inside the cancer cells, the cancer cells will revert into normal cells.
In the book Cancer & Natural Medicine — A Textbook of Basic Science and Clinical Research, author John Boik identifies a dozen substances which have been shown in vitro to be able to revert cancer cells into normal cells (he calls it “differentiation”). All twelve of these items are anti-microbial. So it is a matter of getting these substances inside the cancer cells.
In the Boik book, DMSO is used to get these microbe-killing substances inside the cancer cells. DMSO is so important it is mentioned in its own table, Table 2.3.
In Atlanta, Georgia, a medical doctor was curing cancer patients using DMSO and very low dose chemotherapy (about 10 percent of a normal dose). Why was such a low dose so successful? Because the DMSO allowed the chemotherapy to target the cancer cells and avoid damaging healthy cells. This doctor was shut down by the FDA. Using DMSO in a cancer clinic in the United States is a magnet to get the FDA to raid the clinic.
This website calls his treatment DPT (DMSO Potentiation Therapy). As far as we know, the ICRF, Boik, and the medical doctor all made their discoveries independently.
This is precisely why the ICRF recommends a cancer patient take MSM before they use chemotherapy (not that we endorse chemotherapy). Some of the MSM converts into DMSO, once inside the body, and the DMSO may help some of the chemotherapy target the cancer cells.
Some clinics use the combination of insulin and chemotherapy. This treatment also uses low-dose chemotherapy, but it is combined with insulin, which to some degree also targets cancer cells. This is called IPT or Insulin Potentiation Therapy.
Vitamin C, which also kills microbes, is also used as an IV for cancer patients. The ICRF has tried to get these practitioners to add DMSO to their protocol to open up the ports of the cancer cells, but practitioners rarely listen to researchers.
There are likely many natural molecules which cure cancer by killing the microbes inside the cancer cells, but which have not yet been identified as working in this manner. Vitamin C and Vitamin D3 are good examples. These are highly anti-microbial vitamins which cannot possibly kill cancer cells, so the only way they can treat cancer is by killing the microbes inside the cancer cells (in the case of Vitamin C, hydrogen peroxide is also made).
The number one plant or herb in the world, which has been identified as successfully killing H. pylori is turmeric. Turmeric is also one of the top herbal treatments for cancer. This website combines turmeric (or curcumin, which is more powerful) with honey. Ginger is also used with honey. Both of these combinations are known to have cured cancer by themselves. And we combine honey with cinnamon.
It is much easier to kill microbes than to kill cancer cells if the substance can get inside of the cancer cells. DMSO, MSM, and honey are all “Trojan Horses” to get microbe-killing substances inside of cancer cells. Maple syrup or molasses is commonly used with baking soda and has been very successful. I have received several testimonials from people using this combination (i.e. the Kelmun protocol) to treat cancer or shrink tumors.
For several years, the ICRF has been involved in researching ways to revert cancer cells into normal cells by killing the microbes inside the cancer cells. The reason for this research is that these protocols can work much faster than protocols which kill cancer cells because there is no debris from dead cancer cells. This is the ideal way to cure cancer. On the other hand, building the immune system is a slower process, but is a very good method.
Ultraviolet light has also been researched over the years and the ICRF is researching the use of this protocol. There is a UV light protocol mentioned in the “Inexpensive Cancer Treatments” article. This protocol has created harmless Herxheimers so we know it does kill microbes in the bloodstream.
This protocol, if used properly, kills microbes in the bloodstream. This is an immune-building process, so it is slow working, but getting rid of the microbes in the bloodstream is a cancer treatment because it does build the immune system.
But no matter what a cancer patient does, there should be something in the protocol to deal with the microbes inside the organs so that the immune system can be function properly. Otherwise, cancer may come back.
Dr. Bob Beck's contribution
A normal person will not be diagnosed with cancer in their lifetime. The reason is that there is enough of a balance between the power of their immune system and the number of cancer cells such that the cancer cells do not get out of control.
However, what most people do not understand is how sophisticated and potent the immune system is if it is fully functioning. In fact, it is extremely rare (if it has ever happened) when someone's immune system is fully functioning, which is why so little is known about the power of the immune system.
Natural medicine researchers can supercharge the immune system beyond imagination. But orthodox medicine researchers never work with natural medicine researchers, but orthodox medicine researchers control 99.999 percent of the research money. So while much is known about how to supercharge the immune system (natural medicine), little is known about what the immune system looks like when it is supercharged (orthodox medicine).
For example, what is the set of neuropeptides when the immune system is fully functioning? No one knows.
It is a fact that if a person's immune system was fully functional no one would ever get cancer. This would be a scenario that orthodox medicine never wants to see.
What is known is that the immune system creates two key anti-cancer molecules called: interleukin and interferon. These molecules are called neuropeptides or nerve proteins. There are more than 2,000 different types of neuropeptides in the body, but the cancer-fighting effects of most of them are unknown. In fact, no one knows how many different types of neuropeptides could be created by the body.
Interleukin and interferon, and likely several other neuropeptides are absolutely deadly to cancer cells.
The problem is that the human body generally does not produce an optimal amount of these neuropeptides. In fact, the body only creates a very small number of these neuropeptides.
The reason is microbes, but not the same microbes that live inside of cancer cells, it is the microbes that live outside of the cancer cells.
The average person has about 2 pounds of microbes in their bloodstream and in other places in their body. It is these microbes which interfere with the immune system's ability to create these key neuropeptides.
How do we know this?
The reason is the Bob Beck Protocol. This protocol is a simple electromedicine device which completely cleans the blood of microbes within a few months. It originally was designed as a cure for AIDS, which it is, but it also turns out to be a cure for cancer in many situations (but not for very advanced cancer cases because it can take too long to become effective).
The question is this: How does this simple protocol cure cancer?
The reason is that when the body has no microbes in the bloodstream the immune system becomes supercharged as it can in no other way. The body makes the neuropeptides in “large” amounts (this is a relative term, not an absolute term).
The neuropeptides, when the immune system is supercharged by getting rid of the microbes, quickly destroy the cancer cells.
It can take six months for the Bob Beck Protocol to get rid of all of the microbes in the bloodstream. (Note: The protocol should continue for life or the microbes will come back.) Exactly how long it takes the immune system to be fully recharged is unknown, but likely the immune system starts to become effective against cancer within six or seven weeks of starting the protocol.
The contribution of Dr. Bob Beck, Ph.D. (his Ph.D. was in physics and he taught physics at USC in California) should not be underestimated.
The point is that the Bob Beck Protocol should be used by every cancer patient who is not on chemotherapy or other toxic drugs (there are also a few alternative cancer treatments which should not be used with the Beck Protocol). These drugs cannot be used with electromedicine because of electroporation, which is a phenomenon which would allow the drugs to get inside of the wrong cells.
However, the Bob Beck Protocol should not be the primary cancer treatment at the beginning of the treatment. It can take three or more months for the protocol to make a difference. Other protocols, which start working much more quickly, need to be used at the beginning of a treatment for an advanced cancer patient.
Herbal products should not be used within two hours of the Bob Beck electromedicine devices.
Supplements help build the immune system
It has been known for many years that some plants and other natural substances help build the immune system without getting rid of all of the microbes in the bloodstream. Certain mushrooms have been particularly identified as being helpful for the immune system.
So, is it a good idea to take glucan to help prevent cancer? From Dr. Vaclav Vetvicka, Vice Chairman and Director of Research at the Department of Pathology and Laboratory Medicine at the University of Louisville: “Yes. Glucan will help protect you against cancer and many other illnesses that would normally be eradicated by a fully functioning immune system.” — Beta Glucan: Nature's Secret, p. 49.
The only brand of glucan suitable for my readers is the Transfer Point Brand. Click here for more information on unlocking your immune system; or call (800) 746-7640 to speak with Better Way Health, the experts on Beta Glucan.
(I used to recommend the 4Life brand of Transfer Factor Plus. I have since discovered research from a well-known university that scientifically proved this product is 160x less effective than the Transfer Point Beta Glucan.)
Here is a list of other immune builders:
- A Beta Glucan Supplement: “Beta-1,3D Glucan” [made by Transfer Point] (*) [Recommended]
- IP6 (Inositol hexaphosphate)
- Organic Germanium
- MGN3 / MGN-3 (available in the U.S. under the brand name: BioBran)
- An AHCC Supplement: Immpower, ImmunoKinoko, Immune-Assist includes AHCC
- Immune Fx
- Zeolites (heavy metals interfere with the immune system, zeolites remove heavy metals)
- Aloe Immune glyconutrient product (see my Stage IV article)
- Moducare (a sterols and sterolins supplement)
- Garlic — whole bulbs or a supplement designed for immune system
- RM-10 Ultra [Garden of Life]
(*) — product is endorsed by Bill Henderson
My Touchstone Essentials is a vendor of Pure Body Extra Strength (spray), to chelate the blood, and Pure Body (liquid), to chelate the colon:
There are many other products that claim to build the immune system (e.g. Lentinan, PSK, PSP, Coriolan, D-Fraction, Mushroom Immunity Complex, etc.). Be aware that every vendor claims their product is the best and also remember that Cancer Tutor has no lab facilities to test their claims! MGN-3 or BioBran has a single manufacturer, and has been studied in labs, but found to be very ineffective compared to the Transfer Point brand.
However, MGN-3 or MGN3 has been so severely persecuted by the FDA that its availability and brand name changes from time to time.
Many people say that sugar and other junk foods cause cancer. Well, to some degree that is true.
What junk foods do is put high levels of highly concentrated acidic foods in the body. Microbes love an acidic environment.
Thus, junk foods create the perfect environment for the microbes that are in the bloodstream, the microbes in the organs and even the microbes inside the cancer cells.
That is why cancer diets avoid highly acidic foods and focus on whole (i.e. unprocessed), alkaline foods.
Even in natural medicine cancer can come back
Many natural cancer treatments, whether cancer treatments that kill the cancer cells or even revert the cancer cells into normal cells, can have significant regression rates.
One reason was discussed above, the microbes in the organs and / or bloodstream were not identified and destroyed.
In other words, even natural cancer treatments that kill cancer cells or revert cancer cells into normal cells can have the cancer return. If natural cancer treatments don't fix the root cause of cancer, by cleaning the blood, and especially the organs of microbes and parasites, cancer can come back.
How to ‘cure' cancer
In summary, there are several ways to cure cancer:
1) You can safely and gently kill the cancer cells with nutrients, such as laetrile or Vitamin B17.
The Dirt Cheap Protocol is loaded with these types of treatments. And these treatments are very synergistic with each other.
3) You can safely and gently kill the microbes which are in the bloodstream and thus supercharge the immune system to create interleukin and interferon and other neuropeptides, which in turn kill the cancer cells (e.g. the Bob Beck Protocol or High RF Frequency Generator with Plasma Amplifier devices),
(Note: The High RF Frequency Devices are direct cancer treatments. They not only kill the microbes in the bloodstream they also kill the microbes inside the cancer cells and revert cancer cells into normal cells. So do not compare a High RF Frequency Device with a Bob Beck device.)
4) You can target and kill the parasites and microbes in the organs, which will also help supercharge the immune system (e.g. the High RF Frequency Protocol consultation). On this website, this is called a “liver flush” because the most important parasites are in the liver.
5) You can supercharge the immune system with nutrients. This can also cure cancer though it does not work as fast as some of the other treatments. Many natural plants have been identified which can build the immune system without killing all of the microbes in the bloodstream (or perhaps some of them work by killing microbes in the bloodstream and no one realizes that that is the way they work).
6) You can block the lactic acid cycle with hydrazine sulfate (i.e. hydrazine sulfate) (this is not a direct cure, but it extends the life of the patient so other treatments have longer to work).
7) You can supercharge the non-cancerous cells with nutrients and minerals. Note: this is not a direct cure, but is very commonly used to extend the life of the patient until other treatments can become effective. In fact, it is frequently the first thing that is done. Eniva Vibe is superb at doing this.
A typical cancer treatment will actually do three or four of the above things and maybe all seven of them.
If I were going to use the Bob Beck Protocol I would certainly also use plant and herbal protocols which also help build the immune system, however, I would not use the supplements and herbal products within two hours of the Bob Beck Protocol.
But remember that the Bob Beck Protocol does not start to become effective quickly so it should never be a high priority at the beginning of the treatment.
Cancer is a systemic disease. It is caused by microbes in the organs (which weaken the immune system), microbes inside the cancer cells (which block the production of ATP energy), microbes in the bloodstream (which block the immune system), and so on.