A2: Dear Doctors;
Let’s talk about Cancer and Ph and Quinton Marine Plasma.
Dr Simoncini of Italy is an oncologist whose work with BAKING SODA in the treatment of Cancer clearly supports his concept that some cancers are primarily FUNGAL in origin. His work can be viewed elsewhere on the Internet.
I have heard Patrick Quillin, formerly with Cancer Treatment Centers of America, describe some amazing cases where Colon Cancer simply went away with Nizoral Therapy. Of course, there are others who can show that often a virus is involved in cancer initiation. The article sent by a fact member should help keep us better informed on this important fungal contribution to cancer etiology and treatment.
Baking Soda, as a therapy, brings to mind the complexity of acid-base balance and the need for continual mineral replacement for all of us. We know, for example, that Cesium, Rubidium, Strontium, etc are all strong alkalizers. Cesium has been extensively used in cancers with some documented benefits, but also has a tendency for inducing cardiac arrhythmias that can limit its usefulness.
Today more people are starting to be interested in safe methods for daily total MINERAL REPLACEMENT THERAPY that can be conveniently taken by mouth in a form that the body can utilize. I am convinced more and more that the 10 cc glass ampoules of QUINTON MARINE PLASMA, either isotonic or hypertonic, taken orally and consistently over time is dramatically improving the BIOTERRAIN and restoring cellular function and improving homeostasis. Quinton Marine Plasma glass ampoules work on so many levels that is will take some time for all of us in America to see the true potential of this simple form of therapy that has been used, as a pharmaceutical, in Europe for over 100 years.
Quinton Marine plasma 10 cc glass ampoules supply ENERGIZED WATER but also supply many other useful nutrients from the SEA including amino acids, mucopolysaccaride and RNA. My recent Webinars on Quinton (An update today, Tuesday, October 7th at 4PM MST) have only touched the surface of the vast information I am learning exists in support of the many potential uses for this basic building block for improving the health of everyone on the planet.
We know that we have washed much of the valuable topsoil and thus the trace minerals into the sea. Foods are deficient in these vital ultra trace minerals. Quinton restores these minerals to our bodies in a totally usable form restoring cell-cell communication and homeostasis.
Garry F. Gordon MD,DO,MD(H)
President, Gordon Research Institutehttp://www.gordonresearch.com
The Fungal Nature of Cancer
by R. Gdanski
By reference to information posted on the Internet, I can demonstrate that:
l Cancer tumors are composed of fungal tissue called ergosterol.
l The mechanism of chemotherapy is to block or destroy ergosterol.
l The fungal enzyme fumonisin blocks normal growth, knitting and healing processes.
l Cancer, in the sense of rapid and out-of-control growth, initiates from an invasive fungal infection. The repair-of-injury process initiates rapid doubling of mature cells for repair.
Fungi inside the cells, or nearby, also multiply rapidly. Fungi produce fungal enzymes that prevent knitting and healing. As a consequence, the autonomic repair-of-injury process becomes trapped into a continuous rapid doubling of fungal cells. That's cancer.
l The cause of cancer is well known, and effective cures for cancer are available.
This cause-of-cancer theory is elegant in its simplicity. Human cells produce human tissue.
Parasitic fungal cells produce fungal tissue. There are no defective human genes, no oncogenes and no suppresser genes that fail to function. The repair-of-injury process initiates rapid growth, and lack of healing sustains it. Malignancy is dependent upon rate of fungal growth. Cancer is an all-natural fungal disease.
Mushrooms, a fungi, demonstrate the capacity for fungi to produce a fruiting body, complete with growth factors, a skin-like covering, structural parts, arteries, blood-like internal fluid, and reproductive spores. For information on fungal tissue, surf for plectenchyma, or go directly to http:// http://www.esb.utexas.edu/mycology/bio341/pdf_files/mic321_topic11.pdf
. Here you will observe that there are 3 main types of fungal tissue:
1) aggregates composed of fungal hyphae fusions called granuloma or cysts; 2) growth factor that infiltrate host tissue as found in polyps; and 3) morphologically distinctive tissue as found in tumors.
Up to 96% of cancers initiate in epithelial tissue, because fungi produce competitive enzymes and growth factors. There are no tumors formed of any tissue fungi do not have, such as muscles.
About 70% of a membrane is composed of fibres in the extracellular matrix that knits cells together. Cancer occurs in the extracellular matrix of cells when fungal enzymes and tissues block normal growth and healing. Cancer in infants and children occurs, not necessarily due to an injury, but due to the normal rapid growth capacity of the infant cells. An abundance of growth factor receptors in the cell wall accounts for rapid growth. This theory is the only theory capable of explaining cancer tumors in children, when the tumor is too large to have generated from a single renegade cell within the child's lifetime.
The Fungal Processhttp://www.dundee.ac.uk/biocentre/SLSBDIV4ebl.htm
offers the following picture of cancer cells. Here you can see the fungal ergosterol forming a "keratin pearl" or necklace around one cell with clawlike strands branching out to enclose a second cell. You are looking at the essence of a cancer cell with ergosterol "dedifferentiating" human tissue.
The fact that ergosterol stains differently than human tissue provides a mechanism to identify it.
The website http://www.polysciences.com/shop/assets/datasheets/316.pdf
offers for sale the Fungi- FlurTM staining kit that is used for the "rapid identification of various fungal infections". One single kit will stain 11 fungi, 9 bacteria, and 3 tissues. The 3 tissues are collagin, elastin and keratin.
Cholesterol is not mentioned. The same stain is used to identify keratin and fungi because they have the same ergosterol base. That's why we can see ergosterol in the above photograph of a cancer cell.
Every known cancer observation can be explained if you realize cancer initiates within a mass of fungal-infected human cells. Carcinogens do not cause genetic defects. Carcinogens are of 3 types: toxins and pollutants that block normal cellular function allowing fungi to thrive; fungi and parasites that cause injury and infection; and conditions that prevent rapid healing.
The early warning signs of cancer and the known causes of cancer also fall into these categories. Smoking, for example, causes cancer by causing fungal infections. Tobacco contains fungal residue, spores and fumonisin. Drawing air through a tube containing fungal spores and toxins results in fungal infections. Some parasites cause cancer, some don't. Parasites such as larvae that burrow into colon walls, for example, cause injury and infection. Physical injuries that do not heal also cause cancer by allowing infections to persist. Unexplained persistent bleeding, the most common early warning sign of cancer, indicates fumonisin is possibly present.
Cancer Industry Knows Fungi Cause Cancer The most amazing evidence that the cancer industry knows fungi cause cancer can be found by researching the mechanism for chemotherapy. The 1927 Nobel Prize in Chemistry was awarded to Dr. Heinrich Otto Wieland M.D. for "his investigations of the constitution of the bile acids and related substances". Ergosterol is named from the common grain and corn fungi called Ergot, from which the cell-wall membrane was named. Cholesterol was named for the Greek word "Chole", for bile, from which it was first identified. Since about 1927, the mechanism of toxic drugs to cure cancer has been to block ergosterol or kill fungi.
A web search for chemotherapy and ergosterol will amaze you. Here you will find hundreds of medical university cancer-related sites. The following university lecture http://www.kcom.edu/faculty/chamberlain/Website/Lects/Fungi.htm#classif
describes how chemotherapy functions. (I have added boldface type for emphasis of the ergosterol-blocking mechanism statements.) The lecture notes read as follows:
Antifungal agents are classified according to their chemical structure as macrolides, azoles,allylamines, pyrimidine analogs and miscellaneous.
The polyene antifungals are amphotericin B and nystatin which bind to ergosterol in the plasma membrane, thus disrupting it.
The azole antifungals include fluconazole and keto-conazole plus numerous others. They all block ergosterol synthesis by binding to cytochrome P-450.
The allylamines include naftifine and terbinafine which inhibit squalene epoxidase, thus blocking ergosterol systhesis.
The pyrimidine analogs such as flycytosine incorporate into RNA and/or DNA, thus blocking protein synthesis or DNA systhesis.
Purpose of Chemotherapy
I'll bet you thought the function of chemotherapy was to kill all rapidly growing cancer cells.
Whatever gave you that idea? Is there a cover-up in progress?
we learn that "P450 enzymes (mentioned above) constitute a superfamily of haemthiolate proteins, widely distributed in bacteria, fungi, plants and animals. The enzymes are involved in...both exogenous (outside of cell membrane) and endogenous compounds." Haemthiolate means these enzymes substitute sulfur for oxygen, making the resulting tissue more solid. In addition, information on the fungi, Fusarium can be found here.
Fumonisin From Corn & Grain Products
Fusarium plays a pivotal role in the cancer process. The study of Fusarium led to the discovery of an enzyme which became known as fumonisin. Fumonisin blocks the growth of animal cells by blocking the knitting process of cholesterol fibres. Fumonisin can be ingested in food made from corn or grain products. Calves and colts are often still-born due to this problem. Racehorces and cattle have died from fodder containing fumonisin. Fumonisin explains why infected injuries do not heal.
Estrogen Therapy Spreads Fungal Infection Urine collected from pregnant mares, used as a source of estrogen, also contains fungal estrogenand fumonisin from the fodder. These fungal growth factors cause abnormal growths. That's how estrogen therapy causes cysts and breast cancer. The same applies to hormonal therapy for prostate cancer Further proof that all cancer tumors are formed of fungal tissue can be found by surfing the web for "keratin pearls". Keratin pearls are another name for ergosterol. Here you can view thousands of photographs of cancer tumors.
Fungi in Heart and Stroke Disease
You will also find arteries blocked with ergosterol. Suddenly you will realize the cancer industry knows fungi cause cancer, and the heart and stroke industry knows fungi cause hardened arteries, blocked arteries and heart attacks.
John Hopkins U Patent States Case
The most useful proof that fungi cause cancer, can be found at the Patent Office. To review an effective but suppressed cure for all fungal related diseases such as cancer and diabetes, go to the United States or Canadian Patent Office and look up "fatty acid syntheses". Locate the 1992 patent document number 2,181,031: Inhibitors of fatty acid syntheses as antimicrobial agents. Also go to the John Hopkins University website for additional details. Here you will discover, pardon me, uncover, a patent for a non-toxic method to block ergosterol production.
The mechanism is very simple. Fungi must first make a fat or lipid (sterol) to make ergosterol.
Fungal cells can only make sterols from carbohydrates. Human cells can make sterols from both carbohydrates and ingested fats. By blocking the enzymes required to produce sterols from carbohydrates, fungi cannot produce ergosterol. However, human cells can continue to produce cholesterol from ingested fats and stored fats. As a consequence, there is no toxicity to the human cells, but fungi cannot multiply.
By reviewing the patent claims, you learn that the fatty-acid-synthesis blocker is a common drug called cerluenin. Stedman's Medical Dictionary defines cerluenin as effective for stimulating digestive secretions, gallbladder contractions, and release of insulin. It also inhibits fatty acid synthesis. [from: Cephalosporium caerulea, from which it is isolated] (Hydrazine sulphate acts inmuch the same manner in cancer patients - Editor, Alkalize For Health).
Ergo: There is a Non-Toxic Cure for Cancer Obviously, the cause of cancer has been known for decades. There is a non-toxic cure for cancer and all fungal diseases. Think about it. The medical monopoly in health care is the primary cause for the modern era of fungal epidemics. Toxic drugs that destroy the immune system function are a major cause.
Would you like to do something about it, or just become another victim? Why not learn how to eliminate the conditions that allow fungi to thrive in your body?
©Copyright 2002, R. Gdanski. All rights reserved. Permission hereby granted to duplicate this report with appropriate references.
Reprinted from Planetary Association for Clean Energy Newsletter Volume 11, Number 4 & 5, February 2003, pages 26 - 28.