The Viral-Bacterial-Fungus-Cancer Link

The microbe (virus, bacteria, fungus) has long been associated with and identified as a possible cause for cancer. A large and significant number of independent cancer researchers, scientists, microbiologists and prominent medical practitioners over the past 100 years have found over-whelming evidence supporting this link between cancer and the microbe. They have also discovered and observed that this microbe is pleomorphic (form-changing), meaning it changes back and forth from (harmless) spore form to (harmful) virus form, bacterial form and yeast-like fungus form. This microbe, they have found, is always present in cancer/tumor cells. The below table outlines the research supporting this link.
1890 |
On December 3, 1890 William Russell, a pathologist in the School of Medicine at the Royal Infirmary in Edinburgh, gave an address to the Pathological Society of London in which he outlined his histopathologic findings of "a characteristic organism of cancer" that he observed microscopically in fuchsine-stained tissue sections from all forms of cancer that he examined, as well as in certain cases of tuberculosis, syphilis and skin infection.
The parasite was seen within the tissue cells (intracellular) and outside the cells (extracellular). The size of Russell's parasite ranged from barely visible, up to "half again as large as a red blood corpuscle." The largest round forms were easily seen microscopically. The large size of some of these bodies suggested a fungal or yeast-like parasite. Russell provisionally classified the parasite as a possible "blastomycete" (a type of fungus); and called the forms "fuchsine bodies" because of their bluish-red staining qualities. |
1901 |
After three years' work at the New York State Pathological Laboratory of the University of Buffalo, Harvey Gaylord confirmed Russell's research in a 36-page report titled "The protozoon of cancer", published in May, 1901, in the American Journal of the Medical Sciences. Gaylord found the small forms and the large sacs characteristic of Russell bodies in every cancer he examined. Some large spherical bodies were four times the diameter of a leukocyte (white blood cell). Red blood cells measure about 7 micron in diameter and leukocytes are 2 to 3 times larger than red blood cells. Thus, some of the bodies that Gaylord observed attained the amazing size of around 50 micron in diameter. In addition, he found evidence of internal segmentation within the larger bodies "after the manner recognized in malarial parasites." The tiniest forms appeared the size of ordinary staphylococci. |
1920 |
In the 1920s James Young, an obstetrician from Scotland, repeatedly grew pleomorphic (having many forms) bacteria from various cancers. The microbes had a "specific life cycle" and "spore stages" comprised of exceedingly tiny and barely visible spores. In the laboratory these tiny spores transformed into larger coccoid (round) forms, rod-forms and yeast-like forms (similar in size to Russell bodies). Young found his microbe in 16 cases of breast cancer, and in two mice with breast cancer. He identified "spore forms" and clumped "spore balls" in microscopic sections prepared from the mouse tumours. |
1925 |
In 1925 Northwest Medicine published two papers by Michael Scott, a Montana surgeon who learned about the cancer microbe in TJ Glover's lab in 1921. Scott's microbe was similar to Young's. The parasite had a life cycle composed of three stages: a coccus, a rod, and a "spore sac" stage. Scott believed cancer was an infection like tuberculosis and attempted a vaccine treatment, but his treatment methods were quickly suppressed by the medical establishment. |
1925 |
John Nuzum, a pathologist and physician at the University of Illinois College of Medicine, reported a pleomorphic coccus he repeatedly isolated from breast cancer. The tiniest forms were virus-like and passed through a filter designed to hold back bacteria. Nuzum grew his "micrococcus" from 38 of 41 early breast cancers, and from the cancerous lymph nodes and metastatic tumours resulting from spread of the cancer to other parts of the body. During his 6 years of intensive bacteriological study, he learned the microbe could pass through a filter designed to hold back bacteria, indicating that some forms of the microbe were as small as the size of some viruses. With special stains he detected these small round coccoid forms within the breast cancer tumour cells. Although Nuzum couldn't produce cancer tumours in mice, he was able to induce breast cancer tumours in 2 of 5 dogs injected with the microbe.
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1932 |
Royal Raymond Rife studied medicine at the prestigious John Hopkins University, and began his career as a research pathologist and medical researcher. Over his lifetime, Rife was to receive fourteen major scientific awards and honours and an honorary doctorate from the University of Heidelberg for his scientific discoveries. Royal R. Rife cultured tissue from a breast cancer sample, in Kendall medium, and isolated a micro-organism. He followed this experiment with a series of other studies in which he cultured an organism in Kendall media, from tissue taken from a human breast cancer. He then injected this microorganism into 412 healthy rats, and found that without fail they all developed breast cancer. Finally, he was then able to isolate the original microorganism from the tumours which grew in the rats. In the process Rife became probably the first person ever to fulfil Koch's postulants, for cancer causing microbes. Koch's Postulants are a set of rules to prove the causation of disease by microorganisms. They state that to prove such causality the microorganism must first be isolated and cultured. It must then be shown to have infected a health animal, and finally the same organism must be recoverable from the now infected animal. The cancer virus which Rife named Cryptocides Primordiales or the BX virus, was a minute 1/5 micron in length and 1/20 micron in width. It was highly motile, aerobic (requiring free oxygen for its survival) and highly pathogenic. Rife discovered that while exposing the virus to a temperature of 42C for 24 hours would kill the virus, it remained unaffected by exposure to either X-ray, UV or Infra-red waves. While the discovery of a cancer virus was in itself an incredible feat of scientific endeavour, Rife was to make yet more discoveries destined to rock the scientific status quo. The BX virus was shown to be a polymorphic virus, able to change its states according to the culture in which it was grown. When a BX virus was cultivated in a different media, it was seen to change into a BY virus. When the media was changed yet again it developed into a monococcoid in the monocytes of the blood, and with a further change of media it morphed once again, this time into crytomyces pleomorphia fungi. At any stage along this journey of polymorphism, the original BX virus could be grown again by adding any one of these forms to the original media. |
1935 |
Another Pleomorphist, Canadian researcher of Dr Gruner was watching Rife's work with interest. Gruner was using asparagus agar to grow fungus from cancer blood. Rife was growing a virus from cancer tissue using Kendall media. In the 1930's both Gruner and Rife collaborated and went on to discover that when a sample of Gruner's fungus was cultured on K media the BX virus emerged. By changing the media they could turn a fungus originally grown out of cancer blood into the BX organism, itself grown out of cancer tissue. They repeated this experiment hundreds of times with exactly replicable results each time. |
1940 |
Caste Livingston, independently discovered the cancer microbe in the late 1940s. Aided by microbiologist Alexander-Jackson, who supplied the bacteriologic expertise, the two women found a special stain (the acid-fast stain) that allowed the microbe to be recognised in culture and within the cancer tumour. Like the researchers back in the 1920s, they confirmed the microbe was filterable; and electron microscopic photos provided further proof that the filterable forms were indeed viral-size. Livingston has written three books on the cancer microbe: Cancer: A New Breakthrough (1972), The Microbiology of Cancer (1977), and The Conquest of Cancer (1984).
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1950 |
In the 1950s Irene Diller of the Institute for Cancer Research at Fox Chase, Philadelphia, discovered fungus-like microbes in cancer cells. Joining forces with the Livingston team, Diller worked with specially bred mice with a proven cancer incidence. By injecting them with microbes cultured from breast cancer and other tumours, she was able to more than double the cancer incidence of the mice. She injected healthy animals with cancer bacteria. When cancer tumours developed she successfully cultured the microbe from the tumours - thus proving that these bacteria were implicated in the production of cancer. Utilising Livingston's methods, Diller also grew the microbe from the blood of cancer patients.
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1950-Present |
In the 1950, Professor Gaston Naessens invented a high-powered light microscope, capable of viewing the tiniest forms of life within blood. With this microscope, Naessens discovered in the blood of animals and humans – as well as in the saps of plants – a subcellular microscopic life form that reproduces, which he christened a somatid (tiny body). The somatid, he found, could be cultured (grown) outside the bodies of its hosts (in vitro, "under glass,"). Naessens also observed that this somatid life form was pleomorphic (form-changing). He observed this somatid life form was limited to 3 stages in a healthy organism – somatid, spore, and double spore – and that these 3 stages where crucial to the organisms survival. What was more amazing, was that Professor Naessens observed that this somatid life form became pathogenic (harmful) when the immune system of the organism was compromised or weakened. He observed these somatid life forms then entered a further 13 stages of development, changing from bacterial into yeast-like fungus forms. (A total of 16 stages) Naessens studied the blood of various degenerative diseases, including rheumatoid arthritis, multiple sclerosis, lupus, AIDS, and cancer, and consistently found the 16 stages of the somatid life cycle present in all of these diseases, as he described in the below diagram. 
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1960-1990 |
In the early 1960s Florence Seibert became so impressed with Irene Diller's research that she quit retirement to help prove that bacteria cause cancer. Back in the 1920s Seibert devised a method to make intravenous transfusions safe by eliminating contaminating ubiquitous bacteria. Later, as one of the foremost authorities investigating the chemistry and immunology of the acid-fast bacteria that cause tuberculosis, she perfected the skin test for tuberculosis that has been used worldwide ever since. In 1938, she was awarded the famed Trudeau Medal, the highest prize given to tuberculosis research. Experiments conducted by Seibert and her research team showed these acid-fast and TB-like cancer microbes were not laboratory contaminants because they were able to isolate bacteria from every piece of tumour (and every acute leukemic blood) they studied.
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1983 -Present |
Dr Tullio Simoncini is an Italian doctor specialising in oncology, diabetology and in metabolic disorders. He has treated and cured many cancer patients with sodium bicarbonate (the strongest anti-fungal chemical known to man), commonly via catheter, and has observed tumors consistently disappear within weeks. His book, “Cancer is a Fungus – The Revolution in the Therapy of Tumours” is widely available. It is Dr Simoncini’s unequivocal belief that cancer and tumors are the result of fungal growth in the body. |
Ridding the Body of Fungus to Overcome Cancer
 Whatever alternative cancer treatment plan you eventually decide on, it is important to have a protocol in this treatment plan that kills the fungus inside of you.
Did you know that most alternative cancer treatments either directly or indirectly kill the yeast-like fungus that causes cancer? Some of these include the Gerson Therapy Diet, the Bob Peck protocol, the Jim Henderson protocol, the Overnight Cure for Cancer, Laetrile (Vitamin B17), 714X, Garlic, Sodium Bicarbonate (Baing Soda), MMS (Miracle Mineral Supplement), the Hulda Clark protocol, and herbal remedies that purify the blood such as Essiac tea to name just a few. This is what all of these cancer treatments have in common - they kill fungus!
Some of these treatment options are more difficult than others, so it is important to find one or more that suits you - because they all effectively do the same thing: kill the fungus.
Powerful Anti-Fungal Cancer Treatment: Crushed Garlic

Garlic has long been used to treat and cure cancer throughout the ages, dating back to Hippocrates who recommended his patients eat large amounts of crushed garlic to cure their cancer.
If you choose to take garlic as an anti-fungal to heal your cancer, a minimum amount to take would be 5-6 cloves of (crushed) garlic per day. There are about 12 cloves per whole pod of garlic. Let them sit for at least 15 minutes after they have been crushed. This amount of time is needed to release an enzyme (allinase) that produces these anti-fungal, anti-cancer compounds.
You can eat the raw or cooked garlic as part of sandwiches or other meals. Studies have shown that garlic supplements do not produce the same anti-cancer, anti-fungal results.
The National Cancer Institute states: “Protective (cancer) effects from garlic may arise from its anti-bacterial properties, or from its ability to block the formation of cancer-causing substances, halt the activation of cancer-causing substances, enhance DNA repair, reduce cell proliferation, or induce cell death. The National Cancer Institute, part of the National Institutes of Health, does not recommend any dietary supplement for the prevention of cancer, but recognizes garlic as one of several vegetables with potential anti-cancer properties.”
http://www.cancer.gov/cancertopics/factsheet/Prevention/garlic-and-cancer-prevention Below are a list of studies undertaken demonstrating the effects of garlic to treat and cure cancer.
1. Natural Killer cells are the most powerful infection fighting cells in the white blood cell arsenal. NK cells kill cancer cells, viruses, fungus and bacteria. A study published in the German Medical Journal "Deutsche Zeitshrift" reports on the results of 7 patients taking 5 grams of garlic daily. They said that "6 of the 7 patients had normal NK cell activity after 6 weeks and that all had normal NK activity after 12 weeks."
2. BBC News: Scientists have uncovered fresh evidence that garlic can protect against some forms of cancer. The research, by a team from the University of North Carolina at Chapel Hill, shows that people who eat raw or cooked garlic regularly cut their risk of stomach cancer by about a half compared with those who eat none. They also cut their risk of colorectal cancer by as much as two-thirds. Lead researcher Professor Lenore Arab said: "There seems to be a strong, consistent protective effect for people who are regular garlic consumers. "It doesn't matter if they're consuming garlic in China or in the United States, the effect is still there." However, the researchers found no such benefit from taking garlic supplements. Professor Arab said it might be possible that this could be that the active ingredients are being destroyed in processing or by sitting on store shelves for a long time. The researchers based their findings on data from 22 previous studies from around the world on the impact of garlic on cancer. Many scientists believe garlic helps prevent stomach cancer because it has anti-bacterial effects against a bacterium, Helicobacter pylori, found in the stomach and known to promote cancer there.
3. The biggest study ever conducted in the history of garlic supplementation, a 7 year long clinical study was undertaken to determine aged garlic extract effects on stomach cancer and serous digestive problems that can lead to gastric cancers. It was performed through collaboration of National Cancer Institute (NCI) and leading Chinese researchers, who tested to see if aged garlic supplementation would significantly effect or reduce precancerous gastric lesions. The clinical study was double-blinded and randomized, with over 3,000 human subjects. It was led by Dr. Mitchell Gail at NCI and Dr. Wei-Cheng You at the Beijing Institute for Cancer Research.
Preliminary results of this study showed that people with the highest intake of allium-containing vegetables, like aged garlic, had only 40% of the risk of gastric cancers as those who rarely ate them. Also from the Chinese study was another surprising finding: when researchers used aged garlic extract in combination with antibiotics to treat people with precancerous stomach lesions caused by the Helicobacter pylori bacteria, 76% were completely healed. “It’s a very large and long-term study. We’re still sifting though the data, but we expect to report on it by the end of this year,” said Dr. Gail.
4. Professor Michael Wargovich at the University of Texas studied the effects of two major purified components of garlic - dialylsulphide (DAS) and S-allyl cysteine. He tested these compounds on two animal carcinoma models and found that tumors could be reduced by 50 to 75% He then gave his controls a prophylactic dose of garlic and then deliberately tried to induce a virulent form of esophageal cancer. He found that garlic completely prevented his experimental controls from becoming infected. He concluded that although the precise mechanism may not be clear, the administration of well tolerated garlic products may confer protection from cancer.
5. In Dr. Earl Mindell's Garlic: The Miracle Nutrient, a 1957 study in the journal Science reported that researchers incubated sarcoma tumor cells with the garlic compound Allinase and S-ethyl-L-cysteine sulfoxide, then injected the tumor cells into mice. Tumor growth was completely inhibited and the mice survived beyond the sixth month observation period according to researchers. Mice injected with the tumor cells only (without the garlic compound), survived only 2 months. In another study, for cancer, it is found to be effective. Trasplanted tumours of Jensen sarcoma in rats regressed, and in some cases, completely disappeared after the injection of 1-3 mg of 'Allicin', an active fraction of garlic was given directly into the tumour. "In 1973," Mindell continued, "a Japanese researcher treated a variety of tumor cell types with fresh garlic extract, then injected the tumor cells into mice. According to the results published in the Japanese Journal of Hygiene, tumor development in the mice was 'reversed.' The same researcher was successful in inhibiting mammary tumors and other sarcomas with a solution of fresh garlic extract." Hippocrates, the famous Greek physician, prescribed eating garlic as treatment for cancers.
6. In a study which appeared in a recent 1997 issue of the American Journal of Clinical Nutrition, New York City's Memorial Sloan-Kettering's John T. Pinto, Ph.D., and colleagues, looked at the effects of major water-soluble compounds derived from aged garlic extract (S-allylcysteine and S-allylmercaptocysteine) on cultured (test-tube) human prostate cancer cells. The study found: 1) "Within 30 minutes of exposure" to either of the compounds, proteins that are usually "hopped up" (present at heightened levels) as prostate tumors grow were suppressed; 2) intracellular levels of the reduced (antioxidant) form of glutathione were increased; and 3) a special enzyme (ornithine decarboxylase) which helps produce those "bad-guy" proteins was blocked. A series of breast cancer studies by Pennsylvania State University's J.A. Milner, and colleagues (Carcinogenesis, 1992 & 1993 and Journal of Nutrition, 1996) reported that aged garlic extract significantly prevented [blocked] breast cancer in both the beginning (initiation) and later (promotion) stages. The compound, S-allylcysteine (SAC), by itself, also reduced the initiation of breast cancer.
7. A study conducted by scientists at the Medical University of South Carolina [MUSC] have proven that garlic and its organo-sulfur compounds are effective inhibitors of the cancer process in glioblastoma, a type of brain tumor equivalent to a death sentence within a short period after diagnosis.
Swapan Ray, Ph.D.(MUSC Neurosciences/Neurology associate professor), Naren Banik, Ph.D. (MUSC Neurosciences/Neurology professor), and Arabinda Das, Ph.D. (MUSC Neurosciences/Neurology post-doctoral fellow) studied three pure organo-sulfur compounds (DAS, DADS, and DATS) from garlic and the interaction each had with human glioblastoma cells. All three compounds demonstrated efficacy in eradicating brain cancer cells, but DATS (with three sulfur atoms) proved to be the most effective, lending more support to previous studies of that particular compound. The study will be published in the September issue of Cancer, which is the premier journal of the American Cancer Society (ACS).
Cancer cells are known to have an incredibly high metabolism, as they require much energy to divide cells for rapid growth. In this study, it has been shown that garlic compounds produce reactive oxygen species in rapidly growing brain cancer cells, essentially gorging them to death with activation of multiple death cascades.
"This research highlights the great promise of plant-originated compounds as natural medicine for controlling the malignant growth of human brain tumor cells," Ray said. "However, more studies are needed in animal models of brain tumors before application of this therapeutic strategy to brain tumor patients."
Banik is highly enthusiastic about this discovery. "Our basic studies will eventually be translated to the clinics for patient care. Although we may have to wait several years before its application to humans, the significance of this discovery is enormous. The benefits from this research to brain cancer patients will bring great satisfaction to the researchers and clinicians who are now trying to find a successful treatment for this devastating cancer."
Although there are several more steps, including animal and human trials, before brain tumor patients could receive garlic compound-based treatments, Ray and Banik are optimistic about the possible applications of their discovery to patient care. Garlic-derived organo-sulfur compounds are small molecules that would not necessarily require complicated methods of delivery for treating brain tumor patients, the scientists said, and by virtue of their natural origin are probably better for the human body than synthetic treatment options.
Ray has already received two R01 grants (combined funding of approximately $2.5 million), one from the National Cancer Institute (NCI) and another from the National Institute of Neurological Diseases and Stroke (NINDS), to support his neuro-oncology research program. He has a productive research team that includes five post-doctoral fellows.
As for those who seek to take advantage of any potential anti-cancer benefits from garlic now, certain rules apply. Ray said people should cut and peel a piece of fresh garlic and let it sit for fifteen minutes before eating or cooking it. This amount of time is needed to release an enzyme (allinase) that produces these anti-cancer compounds. Both Ray and Banik caution the public in eating too much garlic, noting that too much of it can cause diarrhea, allergies, internal bleeding, and bad breath and body odor, among other problems, so it is important to monitor garlic consumption.
8. A major Japanese study by Hiroshima University Hospital, Department of Internal Medicine, Kawasaki Medical School, and Onomichi General Hospital, conducted a human clinical trial on the effect of Aged Garlic Extract (AGE) on colorectal adenomas (tumour growth). Patients enrolled in this clinical study were between 40 and 79 y old, who were determined by colonoscopy to be carrying colorectal adenomas. Among 51 enrolled patients (25 in the active group, 26 in the control group), 37 patients (19 in the active group, 18 in the control group) completed the study. Two dosage preparations of AGE were used. An active, high-dose form consisted of six capsules of high AGE, containing the equivalent of 2.4 mL of AGE daily. The control, low-dose form consisted of six capsules, containing the equivalent of 0.16 mL of AGE daily. Due to IRB approval and ethical reasons, in addition to the blinded manner, a low concentration of AGE was needed to function as the control preparation because patients in both groups carried colon cancer. Each eligible subject was randomly assigned to each test preparation (high dose or low dose) in order of enrolment and took it at a dose of three capsules twice a day for 12 months. Follow-up large bowel endoscopy was performed at 6 and 12 months after intake of either preparation and the endoscopists recorded the location and size of any and all colorectal adenomas (tumour growths). The number of adenomas in the control group proportionally increased to 0.56 ± 0.22 (mean ± SE) at 6 mo after study initiation, and 1.44 ± 0.41 at 12 mo, whereas the number of adenomas in the active group was suppressed to 0.68 ± 0.38 at 12 mo (P < 0.05). The change in the total size of adenomas was similar to the number of adenomas, and there was a significant difference between the two groups both at 6 and 12 mo (P = 0.04). The number of adenomas increased to 0.50 ± 0.29 (n = 4) at 12 mo in the control group, whereas those in the active group decreased to 0.63 ± 0.32 (n = 8) at 12 mo. The total size of adenomas during the period of 6 to 12 mo increased to 2.56 ± 1.04 mm (n = 9) in the control group and decreased to 0.86 ± 1.08 mm (n = 14) in the active group compared with the control group (P = 0.03). Conclusions: The results of this trial, and of previous epidemiological and basic studies that are supportive and consistent with this trial, suggest that Aged Garlic Extract (AGE) has a suppressive effect on progression of colorectal adenomas in humans. This effect seems to be multifactorial and reduces many risk factors of cancer. It is urgently necessary to perform larger scale investigations to confirm this trial and its positive effects.
World Health Authorities Connect the Microbe to Cancer

"The over representation of cancer in a region where there is a high incidence of parasitic disease, and the unique characteristics of bilharzial bladder cancer, indicate the possibility that this parasite plays a role in the etiology of cancer. The presence of chronic bacterial cystitis, complicated by urethral strictures, calculi, diverticulae and paralytic stasis, has been known to induce epithelial changes in the bladder mucosa, which may progress to invasive cancer." [CA: A Cancer Journal for Clinicians, the American Cancer Society - Parasites in the Etiology of Cancer: Bilharziasis [parasite] and Bladder Cancer, 1977, Dr. Elsebai, Professor of Surgery, Cancer Institute, Cairo University, Egypt.
"Schistosomiasis (also known as bilharziasis), an infection with a parasitic worm called Schistosoma hematobium that can get into the bladder, is also a risk factor for bladder cancer. Although this parasite is found mostly in Northern Africa, it does cause rare cases of bladder cancer in the United States among people who had been infected by the worm before moving to this country." [American Cancer Society] |
| According to the US National Cancer Institute, "Being infected with parasites increases the risk of bladder cancer." It is possible that the immune system in a highly parasitised human being is compromised. In attempting to fight off the large amounts of [foreign] parasites, cancer cells that exist in every human being are left alone to multiply - the immune system simply not having enough resources to go around. |
| The World Health Organization (WHO) estimates that over 1.5 million of the total of 10 million new cancer cases a year could be avoided by preventing the infection associated with them. WHO states that "Viruses, bacteria and parasites emerge as the "secret agents" causing millions of cases of cancer" each year. |
| Many cancers are associated with infections (for example, cervical cancer is linked to the human papilloma virus), but there is no stronger link between a human malignancy and a parasitic infection than that between cancer of the bile ducts and a liver fluke called Opisthorchis viverrini. Scientists at the Queensland Institute of Medical Research (QIMR) in Brisbane are part of an international study into the link between cancer and a parasite found in South-East Asia. The institute’s Dr Alex Loukas says bile duct cancer is prevalent in Thailand and Laos, where people eat raw fish. He says the results could be applied to other cancers caused by parasites. "We know from collaborations with our colleagues in Thailand that the cancer is highly likely to be caused by proteins that this worm secretes into the bile ducts as part of its feeding process". |
| [American Cancer Society] Cervix cancer is caused by a virus called HPV. HPV is short for human papilloma (pap-ah-LO-mah) virus. This virus can cause changes in the cervix. HPV is NOT the same as HIV. HPV is not a new virus, but we are learning more about this virus. Almost everyone who has ever had sex has had HPV at some time in his or her life. HPV is spread through sex and it can cause an infection in the cervix. The infection usually doesn't last very long because your body is able to fight the infection. If the HPV doesn’t go away, the virus may cause cervix cells to change and become precancer cells. |
| The Institute for Genomic Research and the International Livestock Research Institute have joined forces to decode the DNA of one of Africa’s most destructive cattle parasites. East Coast Fever is caused by a protozoan parasite carried by ticks. The parasite is known to scientists as Theileria parva. Once injected into the cow’s bloodstream it invades the animal’s white blood cells, causing them to divide uncontrollably, like cancer cells. The multiplying cells clog the cow’s organs, killing the animal within 2 to 4 weeis. Knowledge of the genes that the parasite uses to start this lethal cell division may shed light on the mechanisms that cause human tumours to grow. Research on the East Coast Fever parasite has already led to the identification of a previously unknown mechanism that causes leukemia in mice. |
| A new study links parasites with immunosuppression. Stool specimens taken from 38 children with malignancy and from 92 healthy children were investigated for intestinal parasites. The 38 children with malignancy had lymphoma or leukemia and were considered immunosuppressed. Several different parasites were found in 16 of the 38 patients with immune deficiency (47.3%) , compared to only 16 of the 92 healthy children (17.3%). The incidence of parasites in patients with malignancy who were immunosuppressed was significantly higher than in the healthy control group. [Study performed by Department of Parasitology, Dokuz Eylül University Faculty of Medicine, Ýzmir, Turkey and Behçet Uz Children's Hospital, Ýzmir, Turkey, March 2004] |
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Powerful Anti-fungal: Garlic

Garlic is considered one of the world's most powerful anti-fungal and anti-bacterial agents. It has long been used to fight cancer, dating back to Hippocrates (a physician) who recommended cancer patients eat large quantities of crushed garlic to heal their cancer.
For many years, garlic has taken a back seat to modern medicine, who believed only chemicals could treat cancer. Yet modern medicine is now using garlic to treat cancer again, with many of the world's most respected cancer institutes recognizing its angi-fungal and anti-bacterial properties as a key component to the treatment of cancer.
See bottom of this page (left) for detailed clinical studies demonstrating garlic's abilities to cure and prevent cancer.
| Powerful Anti-Fungal: MMS

MMS (Miracle Mineral Supplment) is a powerful new treatment designed to kill all pathogen (harmful) microbes within your body - including viruses, bacteria, and fungus.
The basic ingredient of MMS is Sodium Chlorite - from the salt family. When it is activated with an acetate such as vinegar or lemon juice it produces Chloride Dioxide within the body. This results in oxidation, killing microbes in the process.
MMS has already been used to cure more than 75,000 untreatable cases of Malaria and HIV / Aids in Africa, and there are a growing number of cancer patients who are surviving cancer using MMS.
Click here for further details.
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Powerful Anti-Fungal: Baking Soda

Baking Soda (Sodium Bicardonate) is a powerful anti-fungal and is often used in medical facilities to treat urinary tract (fungal) infections.
In 1983, an Italian oncologist (Dr. Tullio Simoncini) frustrated with traditional cancer treatments, began treating his cancer patients with sodium bicarbonate. He found that when the sodium bicarbonate (5% solution) was washed over the tumor sites, within weeks the tumors would disappear. They could take it orally for intestinal cancers from the throat to the stomach, to the colon, yet a catheter was needed to flush the tumor sites in other parts of the body.
Listen to this video at www.know-the-cause.com
In the mid 1970's, a healer in the USA (Jim Kelmun) began treating terminally ill cancer patients with sodium bicardonate combined (heated) with maple syrup. He claims 15 years later that 185 of these patients are still alive. Fungus and cancer cells love glucose, so they would be lured to eat the glucose (maple syrup) mix, yet be eating deadly anti-fungal sodium bicarbonate at the same time.
Click here to read orignial article.
Jim Kelmun's Protocol - Mix one part baking soda with three parts (pure, 100%) maple syrup in a small saucepan. Stir Briskly. Heat the mixture for 5 minutes.
Take 1 teaspoon twice daily. Do NOT refrigerate this mixture. Keep it at room temperature, in a dark area, and use it until it starts to separate in two or three days, then make another batch.
Very Important Note: Do not use baking soda which has had aluminum added to it, such as Arm and Hammer. Buy a product, which specifically states it does not include aluminum or other chemicals. This will probably have to be purchased at a health food store or online (e.g. Bob's Red Mill, Aluminimum-Free, Baking Soda).
| Powerful Anti-Fungal: Silver Nitrate (The Overnight Cure for Cancer)
Silver has long been used throughout the ages as an anti-biotic, anti-bacterial, anti-viral, and anti-fungal substance. With the discovery of new anti-biotics, it has largely been ignored in modern medicine over the past 100 years.
The Overnight Cure for Cancer (OCC) uses Silver Nitrrate to destroy microbes (virus-bacteria-fungus) within the body and within cancer cells, DMSO (to deliver the Silver to every cell of the body), MSM to reduce inflammation, and the Magnetic Pulaar to prevent microbes attaching to new healthy cells.
Click here for further details.
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