Systemic vs. Cellular level. At the systemic level, cancer can be described as an imbalance between the strength of the immune system and the number of cancer cells in the body, there being many causes, dietary, environmental, and psychological, that can cause the immune system to weaken. Here, however, we are focusing on the cancer cell itself.
A quick review of aerobic Cellular Respiration |
A normal cell makes a lot of ATP energy molecules from oxygen and glucose to power its functions. Some of the glucose entering the cell is converted to pyruvate. Its 1000's of mitochondria (energy production factories) inside the cell take in the pyruvate and through a two-step cycle utilizing oxygen, make it into 32 ATP molecules. |
Evidence has been mounting for well over a century that a cancer cell is a normal cell that has been invaded by a pleomorphic microbe that blocks cellular ATP production. The microbe proliferates inside the cell, eventually altering DNA in the cell nucleus to cause the cell to multiply without control. (Note that the DNA damage is not the cause of the cancer, but rather an action of the cancer microbe). Each of the new replicated daughter cells carrry microbial offspring. Cancer cells revert to a primitive fermentation method of producing ONLY 2 ATP energy molecules for cellular use, but "greedily" using 15 times the glucose of a normal cell.
The microbe blocks ATP
production in two ways:
Researcher Ron Gdanski has shown that it is a microbe inside cancer cells that causes DNA damage. Such can result in uncontrolled cellular reproduction. Mainstream medicine has actually introduced certain viruses inside cells with defective DNA in order to fix the cells'DNA, demonstrating that microbes inside cells can in fact alter cellular DNA.
Gaston Naessens discovered 16 different shapes and sizes of the pleomorphic "cancer" microbe.
Sometimes smaller than a virus (enabling its access to the cell and its nucleus, where its DNA can interact with and change the structure of the cell DNA). Note that the DNA damage is the result not the cause of cancer. The book: "The Persecution and Trial of Gaston Naessens"describes the 16 phases of the cancer microbe. (Believed by Independent Cancer Research Foundation (ICRF) and others to be the cell wall deficient bacteria Helicobacter Pylori.). Eminent researchers (Mostly M.D.s or PhDs) have concurred that a cancer microbe is the final step in the process of a cell becoming cancerous and cite various forms of microbes (including fungi, bacteria, viruses and parasites) as the cancer "villains" E.g. Antoine Béchamp, Royal Rife, Gunter Enderlein, Gaston Naessens,Hulda Clark, Alan Cantwell, William Reich, Tullio Simoncini, and others. Some of these researchers claim to have seen these microbes "morph" from one form to another, lending support to the increasingly popular theory of pleomorphism.
The cancer microbe changes its shape and size based on the acidity or alkalinity of the inside of the cell.
This is of particular significance when we consider using alkalinity treatments (E.g. Cesium chloride/DMSO or baking soda/maple syrup) to eliminate cancer cells. As the alkalinity inside the cancer cell decreases▼ (i.e. the acidity increases▲), the size of the cancer microbe increases ▲. Any therapy that gradually increases the alkalinity▲ of the cell interior, will cause the microbe to decrease in size▼ until it goes into its hibernation form. Called the microzyma, somatid, protit or other names, depending on the scientist that named it. In this hibernation form, it has been found to be indestructable:
"... over the years somatids were revealed to be virtually indestructible! They have resisted exposure to carbonization temperatures of 200 degree C and more. They have survived exposure to 50,000 rems of nuclear radiation, far more than enough to kill any living thing. They have been totally unaffected by any acid. Taken from centrifuge residues, they have been found impossible to cut with a knife, so unbelievably impervious to any such attempts is their hardness."
Book:"The Persecution and Trial of Gaston Naessens"page 5
As the microbe "sleeps", the cancer cell seemingly reverts to normal. Now that the microbe is not intercepting glucose and producing mycotoxins. However, if conditions again become more acidic, the microbe will come out of hibernation and cancer will return to the same cell. A gradual alkaline treatment is thus simply buying time to use another cancer treatment to restore efficient immune sytem function, such as the Beck Protocol. Alternatively, the patient must maintain a lifetime alkaline diet to prevent "waking up" the microbe. There is a possibility that If an alkaline treatment rapidly "shocks" the cell into alkalinity, the microbe may be killed outright and not go into hibernation.
Metasasis occurs when the cancer microbe goes "walk-about"
Some kinds of cancer spread quickly when the cancer microbe exits the cell, travels through the blood and creates a new "colony" of cancer cells a distance from the original colony. Squamous Cell Carcinoma, melanomas, sarcomas and uterine cancer have all been identified by ICRF researchers as spreading this way.
Quotes from Four Women Against Cancer by Dr. Alan Cantwell, M.D.:
"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." Pages 53-54
"More importantly, the Dillers 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".Page 47
(The Dillers were members of the Virginia Livingston, M.D. research team)
Killing the microbe(s) inside cancer cells is the ideal way to deal with cancer
If we can get a microbe-killing "substance" inside the cancer cell . . .
Microbiologist Dr. Royal Rife (in 1930's) had a 100% cure rate for cancer. He utilized electromedicine with at least two frequencies:
Cancer = Microbially infected injuries
The FDA shut Rife down when he refused to sell his technology to the American Medical Association, since he knew they would bury his work. Today, Rife's two machine types have been replicated and improved upon in the "HIGH RF FREQUENCY GENERATOR" family of instruments, to provide gentle electromedicine that sweeps through chosen frequencies. Although not cheap, these devices are readily available on the internet for ~$2300 or ~$4700 including shipping, depending on the power of the amplifier you choose.
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 of these substances are anti-microbial. Cancer & Natural Medicine - A Textbook of Basic Science and Clinical Research
DMSO - Carrier and Membrane Penetrant can be used in or on the body as a carrier for killer substances. (DMSO is able to penetrate cell membranes)
Antimicrobial substances used in cancer therapies
Such therapies include hydrogen peroxide, sodium bicarbonate (carried by maple syrup), cesium chloride (alkaline cesium carried by DMSO), turmeric (seen to kill H. Pylori). Vitamins C and D3 are antimicrobial and known to act against cancer (Vitamin C produces hydrogen peroxide);
Ergosterol (named from the common grain and corn fungi, Ergot) is a necessary component of fungal cell membranes. Since about 1927, the mechanism of toxic chemotherapy drugs to cure cancer has been to block ergosterol or otherwise kill fungi. :
Cancer = Microbially infected injuries
Smoking causes fungal infections. This as a result of drawing air through a tube containing fungal spores and toxins; tobacco contains fungal residue, spores and fumonisin (mycotoxin produced by the Fusarium family of molds, which is also found in corn, wheat and other grains).
A strongly evidenced theory is that cancer is caused by microbial invasion of cells as a result of weakened cell walls damaged by carcinogens in the body. A microbe is thus able to get inside a healthy cell and cause its aerobic mitochondrial energy production to be put "out of order" i.e. the cell is now a cancer cell.
More than 90% of all cancers start in tissue. Ron Gdanski's model has shown how a tear in tissue creates a small pool of blood. This pool of blood becomes infested with microbes, particularly fungi. These fungi weaken the cell membranes of the cells surrounding the pool of blood and are able to enter into the cell, thus causing cancer. His book, "CANCER: Cause, Cure and Cover-up", gives a large body of evidence from several sources to support his model theory. Following are some examples of substances/conditions that can cause tissue damage:
A special kind of pleomorphic microbe has been identified as the cause of cancer
Dr. Royal Rife did numerous experiments injecting a cancer virus into a healthy mouse, which caused cancer in the mouse. His "Rife Machine", designed to kill microbes by vibrating them to death at their inherent, unique frequency, cured many cancer patients, until the U.S. government authorities shut him down.
Molds SEEN breaking through cell membrane
Research scientist Dr. Robert O. Young, PhD, has watched aggressive molds force their way through the cell membrane of normal cells through a live-blood dark-field microscope.
Microbes came out of tumor cells in culture. Dr. Tamara Lebedewa cut off parts of a tumor and put it in a highly nutritious, sterile culture. Within several days she noticed three-tailed amoeba (trichomonads) swimming in the culture. i.e. microbes from inside tumor cells
Several types of cancer are associated with microbes. it has been known since the early 1950's that viruses could remove and incorporate genes and genetic material in cells. The main viruses associated with human cancers are human papillomavirus (HPV), hepatitis B and C virus, Epstein-Barr virus, and human T-lymphotropic virus. For example:
Cancer cells may be reverted into normal cells (as verified by numerous cancer researchers over the past 70 years). Aerobic energy production can sometimes be restored by about a dozen known natural substances. E.g. DMSO (dimethyl sulfoxide). Books: Four Women Against Cancer and The Cancer Microbe: The Hidden Killer in Cancer, AIDS, and Other Immune Diseases, by Dr. Alan Cantwell, MD:.
Cesium chloride kills cancer cells. One therapy utilizes cesium chloride to raise pH in cancer cell by accumulating the cesium inside cancer cells Cesium chloride is also known to kill microbes. Thus, when a cancer patient receives enough cesium chloride to easily kill the microbes inside the cancer cells, but not enough to kill the cell, one might think that the cancer cells would revert to normal. However, cesium left in the cell also blocks glucose from entering the cell leading to lower ATP production and the cell's death.
This theory states that some microbes can change from virus to yeast to fungus to mold to bacteria to a large bacteria, and back again. They can also change into an indestructible, dormant form that Antoine Bechamp, a contemporary of Pasteur, called a microzyma (a so-called living dust particle, also named a somatid by Naessens and a protit by Enderlein). In this form they do not eat or cause harm. However, UNDER MORE ACIDIC CONDITIONS microzyma mutate into organisms that cause disease. Ultimately, in death, they break down the body and return it to "dust". Note: Viruses differ from bacteria in that they cannot live outside cells, also bacteria can be seen under a standard microscope, but viruses are so small that they can only be viewed with a high-powered microscope, such as an electron microscope.
Which indicates that microbial forms cannot change from one form to another. Obviously, further explanation is needed for understanding how the observations and findings of the following eminent scientists can be interwoven into currently accepted knowledge.
Antoine Bechamp (1816-1908; Professor of Chemistry at the University of Strasbourg) said "Microzymas become by nutrition what they ought to become".
Royal Rife Phd (inventor of the high-magnification Rife Microscope)determined that spores of bacteria could change shapes so that the spore could change into a typhoid bacteria, then into a salmonella bacteria and then into a virus-like organism that he called T-bacillus , that causes cancer.
Edward C Rosenow Sr (served as Director of Experimental Biology for the Mayo Clinic between 1915 and 1944), a well respected microbiologist in the early 1900's, had already claimed that altered environments turn harmless bacteria into pathogens. He claimed to have seen typhoid bacteria change into harmless enteric bacteria by increasing the pH a small amount, and change back again by altering the pH back to its original more acidic condition. Other microbiologists have reported similar findings.
Gaston Naessens claims to have seen the complete 90 hour cycle of resistant bacteria that he called somatids. The cycle takes over 90 hours and has 16 stages. In the last of 16 stages, the mold turns into a thallus sack, which bursts open throwing virus-like bodies or more somatids into the environment. Naessens believed that somatids mutate when the immune system becomes weak. His proposed treatment for cancer is to strengthen the immune system. The drug he advocated is being used world-wide by doctors giving it discretely to hopeless cancer patients.
Professor Gunther Enderlein (1872-1968; zoologist, entomologist) discovered protits while working in a German hospital during WWII. He isolated two mold species (Asperigillus niger, Mucor racemosus) as the cause of many human diseases. The spore form of these molds has 3 stages, which live in the blood and all blood cells causing no harm. Its 1st stage has a diameter of .1 micron, which Enderlein called a protit, which may play a part in reproduction and blood-clotting. The protit copulates with other protits to form spores (2nd stage) and double spores (3rd stage). Triggered by a higher, alkaline pH and beginning as a bacillus that secretes acid to lower the pH, the double-spore can balloon into a complete cell-walled bacteria.Eventually the bacteria turns into a mold that destroys human cells, and may then turn into a virus that causes cancer. Enderlein believed that the growth of the pathogenic bacteria proliferates when the blood becomes too acidic (called acidosis). A change in diet and lifestyle can return pH to normal. Also a vaccine containing forms of protits that copulate with bacteria can revert them back into spores.
Dr. Alan Cantwell, M.D. spent 3 decades observing and studying the "cancer microbe", and says the cancer bacteria is as easy to detect and grow in the laboratory as the bacteria which causes TB or syphilis. Cantwell describes it as cell-wall-deficient, having various forms including cocci, rods, large globoid and yeast-like forms, acid-fast granules, fungus-like forms, and large-body forms.The "cancer microbe"has been reported as a pleomorphic, intermittently acid-fast bacterium closely related to the acid-fast mycobacteria and to Mycobacterium tuberculosis, the acid-fast microbe that causes tuberculosis (TB). http://www.rense.com/general80/canc.htm
William Reich (1897-1957, deputy Director of the Vienna Ambulatorium, Sigmund Freud's psychoanalytic outpatient clinic) - referred to bacteria emanating from energy-depleted cells as "T-bacilli" (the "T" from the German word "Tod", meaning death). He found T-bacilli in the blood of both healthy and sick individuals, but more numerous in the sick.i.e. blood is not sterile. In his experiments, he found it was impossible to destroy the microzyma, the smallest living form of life. In this photo (right), the RBC in the center has a smaller round vacuole with moving bodies within.
Tullio Simoncini, M.D. (Italian oncologist) describes in his book "Cancer is a Fungus"how the body forms a tumor as a defensive reaction against a fungus (particularly candida). Several studies show 79-97% of cancer patients also have Candida.[R.L. Hopfer: 79%; U. Kaben: 80%; W. T. Hughes: 91%; T.E. Kiehn: 97%]
Arthur Isaac Kendall PhD (Director of Medical Research, Northwestern University Medical School Chicago);
Bong-Han Kim (medical surgeon at Pyongyang Medical University and Kyung-Rak Institute who is widely recognized to have discovered the primo-vascular system)
Kwang-Sup Soh (professor at the Biomedical Physics Laboratory, School of Physics, Seoul National University, South Korea);