Thanks to Ronald Gdanski, Author of the book "CANCER, Cause, Cure and Cover-up" (ISBN 0-9685665-0-2), who pioneered this plausible explanation as to the cause of cancer.
Cancer is identified as having unrestrained growth, which can be explained as a process resulting from internal injuries that do not heal due to the presence of infection.
Breaking the membrane of a pre-cancerous lesion initiates rapid doubling of infected cells and the pathogens within them. Lack of healing holds the repair-of-injury mechanism in high gear, doubling pathogens, infected cells and the subsequent mutated cells.
Growth factors or enzymes are essential for DNA doubling and cancer growth. Cancer cells in vitro will not multiply without the addition of a growth factor (E.g. blood serum from calves).
In 1913, cancer researcher Johannes Andreas Grib Fibiger of Denmark proved that an infection of parasitic larvae can cause cancer. He initiated cancer in healthy laboratory mice and rats by feeding them parasitic larvae of a worm found normally in horses. Fibiger received the Nobel Prize in Medicine, in 1926, for discovering a parasite (Spiroptera) that causes cancer. Encyclopedia.com Parasitic larvae eat through membrane walls and initiate the body's normal current-of-injury to increase cell doubling for healing repair, whilst concurrently causing microbes to double production of their membrane growth factors. Parasitic larvae also infect adjacent cells.
A 2016, a research article "Parasite infection, Carcinogenesis and Human Malignancy" (eBioMedicine - Part of THE LANCET Discovery Science) PubMed concluded that host tissue damage during parasite development, along with the actice wound healing, chronic inflammation, and metabolic stress induced by parasite-derived products are the three main carcinogenic mechanisms for certain blood and liver flukes.
A 2025 article "Parasites and Cancer: Unraveling Their Complex Interplay" by Dr. Sameer Sinha, makes references to how certain parasites in the body are shown to increase risk for certain cancers and points out the need for more research. Prozoan infections have been associated with different types of cancer, for instance, Entamoeba histolytica, known for causing amoebic dysentery, has been linked to increased risk of colorectal cancer. Liver flukes, particularly Opistorchis viverrini and Clonorchis sinensis are well-documented to increase the risk of cholangiocarcinoma, a cancer of the bile duct. Schistosoma haematobium, a type of helminth (parasitic worm), is well-established as a risk factor for bladder cancer. Helicobacter pylori is a pathogenic bacterium often found in the stomach, which has gained notoriety for its link to gastric cancer, particularly adenocarcinoma.
In summary, if an injury is infected:
Unrestrained growth of abnormal cells will stop if we eliminate the microbial source of growth factors in our body by eliminating all parasites
Cancer eventually causes body tissue to rot. Rotting tissue attracts fungi, mold and yeasts; so whether fungi is a cause, effect or by-product of cancer, eventually it will be there.
Nobel Prize winner Dr. Otto Warburg proved all cancer cells produce energy through fermentation of glucose. Identical to the process used by fungi to ferment sugars. All the observed traits of cancer cells can be explained by recognizing that cancer starts with a mass of infected cells. These are locked in fermentative metabolism by fungal enzymes. In Dr. Gerson's book on cancer, he stated that when cancer patients came to him he noticed that several diseases were common to his cancer patients. He stated: "I found cancer frequently combined with chronic osteoarthritis, high or low blood pressure, chronic sinus trouble, or other chronic infections ..." . Chronic sinusitis is known to be caused by a fungus. Osteoarthritis is an inflammatory disease and the foods most suspected of creating this inflammation are rich in fungi, moulds and yeasts.
During fermentaion, the transfer of the use of food nutrients for (a) The production of ATP and (b) An increase in growth rate, explains why fermentative cells grow faster than oxidative cells. The loss of oxidative metabolism with the subsequent loss of ATP energy production also negatively affects immune system function and its ability to eliminate pathogens.
Lastly, destroying all rapidly growing cells with toxic drugs will not allow the injury to heal and so shut down the healing current of injury, thus defeating the body's only method to stop rapid cancer growth - part of the reason why chemotherapy is unsuccessful.
http://homodiet.netfirms.com/otherssay/letters/cancer.htm chris gupta