Therapies › Cancer

Dr. Santos' cancer program involves the using of intravenous therapies along with detoxification and diet modification. We modify each patient's plan based on the radiation/chemotherapy schedule, the type of cancer and the aggressiveness of the cancer.

Typically, we use high dose intravenous vitamin C therapy and intravenous sodium bicarbonate which has been shown to act as a natural chemotherapy agent. Many clinics around the globe using High dose vitamin C therapy have documented excellent results. We also utilize a combination of Ozone/photoluminescence to help stimulate the immune system to fight the cancer. These treatments typically reduce the side effects of chemo and radiation.

Intravenous Sodium Bicarbonate for Cancer

Dr. Santos uses the protocol of Dr. Simoncini for the treatment of cancer. Dr. Simoncini's results are promising and Dr. Santos has used his treatments inconjuction with other Natural Immune treatments to treat his cancer patients. Sodium bicarbonate helps to increase the pH of the blood thus making the cancer patient more alkaline. Tumors grow in a low pH or acidic envirmonment.  By increasing a cancer patients body pH and making it more alkaline, chemotherapy, radiation and natural cancer treatments such as intravenous vitmain C and ozone therapy becomes much more effective.

Tullio Simoncini is a Roman doctor specialising in oncology.

Dr. Simoncini discovered that the cause of cancer is a fungus and tried hard to persuade scientists how wrong the actual theories on cancer are. His therapy based on the strongest antifungal substance, sodium bicarbonate, is harmless and very effective and should be adopted all over the world.

This is an example of a colon cancer tumor case:

At the beginning of January, 2000, I visit the patient, who is affected by stenotic adenocarcinoma of the ascendant colon.

The patient’s condition is very critical, to the point that in December, 1999, with a haemoglobin value of 6 mg he had undergone two blood transfusions.

The therapy starts at the beginning of January with appropriate diet, reconstituents and sodium bicarbonate taken orally.

After a few days, the intestine begins to recanalize and normalize evacuation. The patient constantly improves, later reaching even the normalization of the hematochemical parameters (haemoglobin and CEA). Notwithstanding the optimism about the results that have been reached, nevertheless the patient is warned about the dimensions of the neoplasia which cannot be eliminated only orally, both because with this procedure only a barely sufficient canalization is obtainable and because the bicarbonate cannot be assumed for excessively extensive periods.

It is therefore decided to program a cycle, for the end of April to the beginning of May (possibly to be repeated several times). The cycle consists of administrations of sodium bicarbonate solutions through the endoscope.

The intent is that of amplifying the destructive effect the fungin colonies (Candida), which causes the development of the tumoral mass. The endoscopic examinations of April 26, 2000 show that the tumoral mass occludes the intestinal lumen (Fig. 1). The Candida (after the “washing” of the epithelium with water) are well visible (Fig. 2).

Fig 1



Fig 2
 

Fig 3


Fig 4
   

After a day, a dramatic reduction is evident
(Fig. 3), and this is confirmed even in the following days (Fig. 4).
With the endoscopies it is therefore shown that the fungus (Candida) is the causal element of the tumoral masses. It is in fact possible to see them at the sub-epithelial level after the removal of blood with physiological solution, because of their whitish colour. Furthermore, the direct aspersion technique with sodium bicarbonate demonstrates with certainty that it is the only substance able to destroy the fungin colonies that colonize the tissues and generate various types of tumours. It is appropriate to highlight that the action of sodium bicarbonate takes place not only as a correction of acidosis, but also as a specific ability (that is, not possessed by other basic compounds) to destroy fungin colonies. It acts by destroying the connections – the intercellular bridges that exist between the cells – thus preventing them from communicating and becoming a common body against the immune system.

In this way, the fungin cells, now individually exposed to the defence mechanisms of the host, can be easily and quickly phagocitated.

Bicarbonate allows humoral immunity to be effective and to disintegrate the colonies, thus favouring the cicatrisation of the tissues.

Instead, the immune reaction is impotent when faced by colonies already so large that they cannot be intimately penetrated and therefore disintegrated.

The whole mystery of the rooting of the fungi and of the cause of cancer is right here – in the decrease of the effectiveness, up to the extinction of the humoral defensive capabilities when the colonies manage to conquer grounds and to expand enough. The sodium bicarbonate has the ability to completely reactivate the defensive functions of the organism.

This action explains the cases of reversibility and healing of tumours – which occur for various reasons: therapeutic, dietary, or environmental – when the fungin cells, reduced to the size of a colony that is not sufficiently large or consolidated, can undergo changes that makes them individually attackable.

This is the key of the interpretation of the formation of cancer that can develop only if it manages to go beyond the defences of humoral immunity. This is possible only with the convergence of all the factors usually invoked – spiritual conflicts, stress, endogenous and exogenous toxicosis, bad diet, malnutrition and more – that act for a given time period on a given tissue or target organ.

Intravenous Vitamin C for Cancer

Ozone

Ozone: Cancer and its uses in medical therapy

by Dr. Robert E. Willner

Ozone therapy is one of the most powerful and versatile therapies known today. Extensive medical research on Ozone therapy has been done primarily in Europe. Through its mechanism of action, ozone has beneficial effects on every part of the body. The effects include:

1. Inactivation of bacteria, viruses and fungi: Ozone disrupts the intergrity of the cell envelope through peroxidation of the phospholipids and lipoproteins. In fungi, ozone inhibits cell growth at certain stages. With viruses, the ozone damages the viral capsid and disrupts the reproductive cycle by interrupting the virus-to-cell contact with peroxidation. Cells previously infected by viruses are more susceptible to destruction by the peroxide produced through ozonolysis, because they have weak enzyme coatings.

2. Enhancement of circulation: In circulatory disease, a clumping of red blood cells hinders blood flow and becreases oxygen absorption due to reduced surface area. There is a decrease in red blood cell flexibility which prevents them travelling down the tiniest capillaries, and blood viscosity increases. With Ozone therapy, clumping is reduced or eliminated and flexibility is restored, along with oxygen carrying abiltiy. Oxygenation of the tissues increases as the arterial partial pressure increases, and viscosity decreases. Ozone also oxidizes the plaque in arteries allowing the removal of the breakdown products, unclogging vessels.

3. Stimulation of oxygen metabolism: Ozone causes an increase in the red blood cell glycolysis rate. This leads to the stimulation of 2.3-diphosphoglycerate which shifts the oxyhemoglobin disassociation curve to the right. This leads to an increase in the amount of oxygen released to the surrounding tissues. There is a stimulation of the production of the enzymes which act as free radical scavengers and cell wall protectors: glutathione peroxidase, catalase and superoxide dismutase. Ozone activates the Krebs cycle by enhancing oxidative decarboxylation of pyruvate, stimulating production of ATP. Ozone also causes a significant reduction in HADH and helps oxidize cytochromes.

4. Dissolution of malignant tumors: Malignant cells have an increased rate of glycolysis which leads to the production of more lactate. With ozone therapy, there is a significant decrease in lactate production, showing that the metabolism is being inhibited Tumor cells have a peroxide intolerance due to insufficient peroxidase and catalase. Ozone is thus able to oxidize the outer lipid layer of malignant cells and destroy them through cell lysis.

5. Activation of the Immune system: Ozone stimulates the production of interferon and interleukin in the body. From this there is a cascade of subsequent immunological reactions.

6. Formation of peroxides: Ozone reacts with the unsaturated fatty acids of the lipid layer in celllular membranes, forming hydro peroxides. Lipid peroxidation products include peroxyl radicals, vital for killer cell action.

Mistletoe/Iscador

Mistletoe/Iscador injections are also used to help the body fight the cancer. In animal studies, mistletoe preparations have helped fight some forms of cancer. The best results with Iscador are claimed for its use with solid tumors both before and after surgery and radiation. Given 10 to 14 days before surgery, it is thought to help prevent metastatic spread due to surgery and to promote recovery and it is also used for advanced stage, inoperable solid tumors, especially cancers of the bladder, stomach, intestine, genital organs, and skin. It is also claimed that bone metastases are retarded in some cases. Results appear less promising for inoperable cancers of the breast, lungs and esophagus. It is thought that tumor growth slows or stops, and then gradual regression begins. It is believed that tumor cells are transformed first to a semi-malignant form, then to chronic inflammation and finally to normal tissue.

Mistletoe

Mistletoe contains a cytotoxic lectin, viscumin. It also contains a number of cytotoxic proteins and polypetides (viscotoxins). Various lectins are both cytotoxic and immunostimulatory. It induces tumor necrosis, increases natural killer cell activity, increases production of interleukins 1 and 6; activates macrophages; induces programmed cell death (apoptosis), and protects DNA in normal cells during chemotherapy.

Gendicine

Gendicine (p53 gene therapy) is a new drug used in China to cure cancer. The pharmaceutical company has documented many cures of solid cancers through gendicine. Recent published scientific studies show Gendicine is a very effective new treatment for over 40 solid tumor cancers. "Gendicine" is the trade name for rAd-p53 oncogene therapy developed by Shenzhen Sibiono Gene Tech Co. Ltd. Gendicine is the first approved gene therapy in the world. Gendicine was approved for treatment of cancer in October 2003.

Gendicine kills tumor cells selectively by the following mechanisms:

• Triggering apoptosis signal pathway in tumor cells.
• Inhibiting survival signals transduction in tumor cells.
• Inhibiting blood vessel growth and metabolism of material/energy in tumor cells.
• Inhibiting tumor cell's infiltration and metastasis.
• Reversing radiotherapy and chemotherapy drug resistance.
• Arresting tumor cell cycle and keeping them in a deep dormancy stage.
• Initiating the bystander effects, regulation of the immune response to kill tumor cells.

What is Gendicine?

Gendicine in the trade name for a new medication generically known as "recombinant human adenovirus vector p53 gene injection" or "rAd-p53 gene therapy" for short. In October 2003, Gendicine became the first gene therapy to ever be approved in the world. The independent bio-technology company that makes Gendicine is called "Shenzhen SiBiono GeneTech Co. Ltd." The entire story of Gendicine is available on the www.sibiono.com web site.

What is Gene Therapy?

Gene therapy is best explained in this way:
A medication that is able to correct specific defective genetic information in the nucleus of living cells. A gene is a sequence of DNA found on a chromosome in the nucleus of a cell. Imagine that the nucleus of the cell is like an instruction manual for the building and destruction of that cell. The DNA would be like the alphabet in the cell's instruction manual, the genes would be like the sentences spelled out with the DNA, and the chromosomes would be like chapters in the cell's instruction manual... etc.

Our cells all have predetermined jobs to do and a set number of cell divisions and a set time length to live before they all die. Don't worry, all cells divide at a set time to replace themselves with an almost identical new cell to take its place and do its job in the body. This is good, because our bodies function best with young strong cells rather than old weak cells. The main point, is that genes determine the healthy growth and death of the cell. When this natural process is disrupted in any way we experience disease and illness.

If gene defects cause illness, then it is easy to understand that almost all illnesses have a genetic factor involved. It is also understandable the significant benefits we should expect if we have a way to correct a defective gene. Some genes seem more important than others like some sentences in a book are more important for the proper understanding of the story. Some genes are so important that if they are not working then a cell will grow out of control. When this out of control cell growth occurs we call it a neoplasm or CANCER. Any person faced with a cancer will know that as time goes on, the cancer will become even more abnormal in behavior so that it eventually starts spreading to other parts of the body. Even treatments that have some effect in the beginning often become ineffective as the cancer mutates further and becomes resistant to treatment... All this, UNLESS we can correct the defective genes known as "onco-genes" that are malfunctioning and allowing the cell to live and divide unregulated by healthy genes.

The p53 gene is one of the most important oncogenes and it is believed to be directly involved in the genesis of about 60% of all cancers. When the p53 gene is transcribed (read) it produces a protein that initiates cell death. Cancer cells have somehow turned off the p53 gene and thus they have turned off the mechanism of cell death. When the p53 gene is turned off, it doesn't matter how much we stress or poison the cancer cell with radiation or chemotherapy, that cancer cell will resist dying and make therapy ineffective. If the cancer cell is given a new copy of the p53 gene then it will die as soon as that p53 gene is transcribed.

Normal cells have a good copy of the p53 gene and the normal cells have another regulator that makes sure the p53 gene is transcribed at the right time. Normal cells have complete degradation pathways for p53 protein clearance. By giving a cancer cell a new functional copy of the p53 gene we are essentially turning that cancer cell into a normal cell with respect to apoptosis (cell death). The cancer cells that get a functioning copy of the p53 gene will die like it is programed to do when the cell replicates or is stressed in some way.

Gendicine uses something called a vector to target cancer cells and 'insert' the p53 gene into the cell nucleus. This sounds like an easy thing to do, but it is not so easy and it has taken decades of research to engineer a medication like Gendicine.

Even more remarkable is the safety profile of Gendicine. The medication has no known long-term side effects on human cells in 25 years of research. The most common side effect reported a few hours after Gendicine injections are 'flu like symptoms' that last only up to 48 hours after treatment. Gendicine is not available in Canada. Patients are sent to a partner clinic in the Bahamas for treatment (http://www.gendicinebahamas.com). When patients return, they continue the additional treatments at our clinic. 

© 2007 Dr. Rod Santos. All rights reserved. No parts of this web site may be used, borrowed or copied without express written permission by Dr. Rod Santos. Thank you for visitng. The material on http://www.drrodsantos.com/ is for informational purposes only and is not a substitute for medical advice or treatment for any medical conditions. Food Allergy Testing Vancouver Food
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