The root cause of cancer was discovered in 1890 by William Russell (1852-1940). The brilliant Dr. Russell saw microbes both inside and outside of the cancer cells. It was obvious that the microbes inside the cancer cells were the ones causing cancer.

The cancer microbe was studied in detail in the early 1900s and was found to be highly pleomorphic. Many years later another microbiologist, Gaston Naessens, counted 16 different sizes and shapes of the cancer microbe (see The Persecution and Trial of Gaston Naessens by Christopher Bird). The medical establishment in Canada was so delighted with his discovery that they had him thrown in jail.

You see, if cancer is caused by microbes that are inside the cancer cells, then it is easy to cure cancer; just kill the microbes inside the cancer cells. But no medical establishment wants people to know that cancer can be cured. They want cancer to be a mysterious disease that will never be cured.

The size and shape of the microbe is a function of the pH inside the cancer cell. The higher the pH, the smaller the microbe.

The higher the pH the more lethargic the cancer microbes become and cancer spreads more slowly. Natural medicine practitioners take advantage of this fact and frequently use highly alkaline protocols to slow down the spread of cancer and in many cases these treatments can cure cancer.

Also, Dr. Royal Rife, a microbiologist, in the 1930s, also knew that it was microbes which were inside the cancer cells which caused cancer. By knowing this he developed a gentle electromedicine device to kill these microbes. This device had a 100 percent cure rate and it did nothing but kill microbes inside the cancer cells.

The AMA and FDA (Food and Drug Administration) were so incensed that he was curing cancer that the AMA tried to buy him out. When he refused the FDA came in and destroyed his lab and his machines which had not already been sold and delivered.

Researchers since then have found three of his original machines, which had been sold before the FDA destroyed his lab. They have made the specifications of his equipment public information.

Dr. Virginia Livingston's team of cancer researchers discovered why cancer cells have DNA damage. They discovered that the microbes inside the cancer cells get inside the cell nucleus and their DNA mixes with the DNA of the cell, which changes the DNA of the cancer cells.

In fact, the concept that the DNA of a microbe, which gets inside of a human cell nucleus, and thus changes the DNA of the human cell, is at the heart of gene therapy. This is not some strange theory, it is a concept which is used in modern medicine to treat genetic diseases.

My point is that the Livingston team discovered that the DNA damage occurs after the cell is already cancerous (i.e. after the microbes are already inside the cancer cells).

Dr. Livingston designed a vaccine to kill these microbes and obviously died without any recognition from orthodox medicine for her team's critical discovery. Instead, orthodox medicine has ignored her team's discovery and still claims that it is DNA damage that causes cancer. This gives them an excuse to claim that a cure for cancer is 50 years away. A cure for cancer will always be 50 years away according to anyone who is in bed with the pharmaceutical industry, such as the American Cancer Society.

By claiming that DNA damage causes cancer, the public believes that cancer will never be cured. But Virginia Livingston was curing cancer with a vaccine she developed.

This DNA damage (which is a result of cancer, not a cause of cancer), is what all large “cancer research” organizations claim cause cancer. They are spending billions of dollars trying to fix this DNA damage instead of trying to safely target and kill the cancer cells using Mother Nature (who already knows how to target and kill cancer cells) or by killing the microbes inside the cancer cells (which reverts the cancer cells into normal cells), which is how Dr. Rife cured cancer.

The second concept I wish to discuss is regarding the nature of cancer cells. A Nobel Prize was awarded in 1931 for the discovery that the defining characteristic of cancer cells is low ATP energy. ATP is a molecule which is made inside the mitochondria, which is inside of all cells. There are thousands of mitochondria inside of all cells and the ATP is what provides cells their energy.

So why do cancer cells have low ATP energy and who cares if there are microbes inside the cancer cells?

In 2004, an Independent Cancer Research Foundation cancer researcher tied these two major discoveries together by explaining the mechanism of how these microbes, which are inside of the cancer cells, block the production of ATP molecules. In other words, he explained that cancer is caused because the microbes inside the cancer cells block the production of ATP in two different ways.

It is beyond the scope of this article to explain this mechanism, and its ramifications, but if you are interested: What Causes Cancer.

This discovery supported the claim of Dr. Rife that if you kill these microbes the cancer cells will revert into normal cells. They become normal cells again (or for the first time in many cases) because with no microbes inside the cell the ATP energy will be restored and the cell will be healthy again.

This discovery has led to several new, highly effective natural cancer treatments, particularly DMSO, MSM, and honey protocols. The DMSO, MSM, and honey are “Trojan Horses” to get microbe-killing substances inside of cancer cells to kill the microbes.

This discovery has also explained how some previously existing natural cancer treatments worked.

The discovery also led to the fact that some natural cancer treatments would conflict with each other (the conflict is not dangerous, but one treatment may neutralize another treatment). The conflict can occur because one type of cancer treatment is trying to lower ATP energy (to cause the cancer cells to fall apart), and another treatment is trying to kill the microbes inside the cancer cells, which would raise ATP energy because when the microbes are gone, so is the reason ATP energy in cancer cells stays low.

For example, do not mix Paw Paw (which causes cancer cells to fall apart by lowering ATP energy) with the High RF Frequency Protocol, which was designed to kill the microbes inside the cancer cells and thus revert the cancer cells into normal cells. When you kill the microbes the ATP energy rises because there is nothing to block the creation of ATP energy (the microbes are what block the ATP energy).

Thus, one protocol is lowering the ATP energy and the other protocol is incidentally raising the ATP energy. The Paw Paw treatment will be worthless. The High RF Frequency Protocol will work just fine because it is interested in microbes; it is not directly interested in ATP energy.

A different Independent Cancer Research Foundation cancer researcher designed the protocol for using the High RF Frequency Protocol for cancer. It is one thing to have the equipment and another thing to know how to use it.

Let us partially summarize what the cancer microbe does.

First, the cancer microbe largely or totally blocks the production of ATP molecules in the mitochondria (and the cancer cells have to revert to another method, fermentation, to make enough ATP molecules to stay alive).

Second, the DNA of the cancer microbes is what causes the DNA damage of the cancer cells after the cell is already cancerous or is beginning to become cancerous.

Third, the cancer microbe also excretes enzymes that coat the outside of the cancer cells so the immune system cannot identify them as cancer cells and thus the immune system cannot safely target and kill them. The existence of the enzyme coating has been known about for more than 50 years in natural medicine.

In fact, over 50 years ago there were natural cancer treatments (e.g. proteolytic enzymes) that stripped away these enzyme coatings so the immune system could identify the cancer cells and kill them. Dr. Kelley used proteolytic enzymes as part of his treatment.

The existence of this protein coating is proof that DNA damage is not the cause of cancer. How could DNA damage create a coating of enzymes on the surface of cancer cells??

Fourth, Dr. Mathias Rath, MD, who had to flee the United States to avoid being arrested for curing cancer, discovered that these enzymes (or different enzymes excreted by these microbes, we don't know) also cut a path across tissue so the cancer cells could spread more easily.

It is beyond the scope of this article to go any further, but my point is that there has been researcher after researcher who knew about the cancer microbes inside the cancer cells. And there have been a growing number of clever tactics developed to kill these microbes.

When you kill all of the microbes inside of a cancer cell, the cancer cell will revert into a normal cell because there is nothing to block the production of ATP energy. This is the ideal way to cure cancer because there are no dead cells and no debris from dead cells.

But most natural cancer treatments work in other ways.

Some treatments use natural substances that target and kill cancer cells. Laetrile, or Vitamin B17, is a perfect example. Carrots and purple grapes both contain multiple nutrients that can target and kill cancer cells. One researcher thinks that it is the oxalic acid in carrots that cures cancer. He may be right.

Other treatments work by supercharging the immune system and then letting the immune system deal with cancer. One example is Dr. Bob Beck, who had a Ph.D. in physics. He designed a cancer treatment that removed all microbes from the bloodstream and found out that by doing this the immune system was supercharged and the immune system could get rid of the cancer cells.

The problem with building the immune system is that it is a slow process. Many cancer patients today who seek out natural cancer treatments have been sent home to die and do not have the time left to live to have their immune system rebuilt after it had been damaged by chemotherapy. But even these patients can benefit from the Bob Beck Protocol, but it should not be their primary protocol.

While the High RF Frequency Protocol works by killing microbes, primarily inside the organs, which gets the immune system functioning again, it also provides key nutrients to the cells, such as in the immune system, the High RF devices directly energize cells to keep the patient alive, the devices also pump the lymph system, etc.

Some treatments work by using super-nutrients to “keep the patient alive” (so they have more time to treat their cancer) by using special cell-energizing supplements. The Budwig Diet is a good example. The GB 4000, an electromedicine device, is the best way to energize cells quickly (see the “Weak Cancer Patients” article and the “Understanding Treating Cancer” article).

In fact, the best natural medicine treatments today use a combination of tactics. One highly nutritional protocol “keeps the patient alive” and at the same time other treatments are dealing with the cancer cells and yet other treatments are building the immune system, others are killing microbes in different places, etc.

The three most powerful treatments on this website, the High RF Frequency Protocol, Cellect-Budwig Protocol, and Cesium Chloride Protocol are all multi-pronged approaches, and all come with expert support.

These two protocols were combined because we were getting some extremely advanced cancer patients. Using similar logic, the Dirt Cheap Protocol (usually without the Kelmun protocol due to too much alkalinity) can be combined with any other protocol.

Remember that many other treatments can be combined with these treatments. For example, either High RF Frequency Protocol can be combined with any of the other protocols.

Some newer protocols use the technology of killing the microbes inside the cancer cells, such as the High RF Frequency Protocol, the DMSO protocols, and honey protocols. Most of the DMSO protocols are on the website of the Independent Cancer Research Foundation. I support the DMSO protocols because I have been researching DMSO since 2004.

In theory, DMSO could cure cancer in one day, as it does not stress the stomach because it can be taken transdermally (i.e. through the skin). However, we are concerned about Herxheimer's (which is severe brain fog caused by the release of mycotoxins by dead microbes) so we have not tried to cure cancer in one day with this protocol.

However, “brain fog” is not dangerous and a patient who understands what causes brain fog, and can mentally prepare for it, could use very high doses of DMSO and chlorine dioxide (DMSO/CD).

In fact, I probably had the worst case of brain fog in history because I accidentally overdosed on a super-microbe-killing substance used in water treatment plants. It felt like most of my brain was dead. But I knew exactly what was going on in my brain so I just slept it off. So if the patient is old enough to know what to expect, they can be prepared for it.

The MSM protocols were designed to do this also and we hoped they would be as effective as the DMSO protocols (because the MSM molecule is almost identical to the DMSO molecule and MSM does not cause the body odor of DMSO), but so far the DMSO protocols seem to be significantly more effective. However, MSM is used to help clean lactic acid out of the blood and do other things, so it has its own benefits.

My point is that it is common to combine multiple approaches in the same treatment. That is what the experts work on accomplishing.

This is just an introduction to modern natural medicine treatments. Understanding Treating Cancer goes into more issues. You might also want to read What Causes Cancer, which goes into detail about what is going on inside the cancer cell.