- November 22, 2020 at 2:29 pm #198webmasterKeymaster
CESIUM AND HOW TO UTILIZE IT
Cells, whether cancerous or normal can only live and reproduce (undergo mitosis) in a Ph range of between 6.5 and 7.5. A healthy cell has a Ph of 7.35 while a cancer cell is more acidic. Cesium when taken orally will raise the Ph of cancer cells, but not that of normal cells. When the Ph of a cancer cell goes above 7.5 it dies and if it goes above 8.0 it will die in a matter of hours.
WHAT IS IT? IT IS A HIGHLY ENRICHED OXYGEN ALKALINE METALS THAT ARE UTILIZED BY THE CELLS TO KILL OF ANY CANCER CELLS. THE WAY THEY WORK IS BY ENRICHING THE CELLS WITH A HIGHER THEN 7.4 ALKALINE LEVEL LEAVING THE HEALTHY CELLS ACTIVE AND ALIVE AND THE CANCER CELLS DEAD. IT WAS DISCOVERED THAT THE HUNZAS AND THE HOPI INDIANS DRANK WATER THAT WAS VERY HIGH IN POTASSIUM AND CESIUM OR RUBIDIUM….WHEN THEY ( THE 2 CULTURES PREVIOUSLY MENTIONED) DRANK THERE WATER SUPPLY , NEITHER CULTURE HAD ANY CANCER. IT SEEMS ALSO THAT POTASSIUM ON IT’S OWN WITHOUT THE OTHER 2 ELEMENTS IS ONE OF THE BEST CANCER THERAPIES AS WELL, GERSON USED TO GIVE HIS PATIENTS 3 DIFFERENT TYPES OF POTASSIUM AND FOUND THAT AS THE CANCER CELLS DIED OF, AS A RESULT OF THE ALKALIZING EFFECT OF POTASSIUM, THE LEVELS OF POTASSIUM DROPPED DUE TO THE FACT THAT THE CELLS WERE BEING RE FILLED WITH THE DOSE REQUIRED TO MAINTAIN A HEALTHY CELL.
CESIUM CHLORIDE HAS BEEN USED TO RAISE PH OF THE BODY AS AN ALTERNATIVE TO CONVENTIONAL THERAPIES FOR A VARIOUS DIFFERENT TYPES OF CANCER: BREAST, LUNG, PROSTRATE, COLON PANCREATIC, LIVER, SKIN, OVARIAN, STOMACH, CERVICAL, BRAIN, KIDNEY, TESTICULAR, BONE, THROAT, THYROID, GASTROINTESTINAL, GALL BLADDER, METASTIC MELANOMA, CANCERS IN ANIMALS SUCH AS CATS, DOGS AND HORSES
IT CAN BE USED ORALLY AS WELL AS INTRAVENOUSLY. IN ALL LIKELIHOOD IT WOULD BE COMBINED WITH POTASSIUM OR RUBIDIUM, AND POSSIBLE VITAMIN C , DUE TO THE FACT THAT VITAMIN C BECOMES ALKALINE IN THE BODY, AND AS A FREE RADICAL SCAVENGER, AND ANTIOXIDANT AGAINST CANCER.
Cesium Chloride / High pH (Oxygenation) Therapy
Cesium is one of the most alkaline elements and raises the pH (oxygen content) of the body’s cells. Otto Warburg earned a Nobel prize for showing that cancer thrives in anaerobic (without oxygen), or acidic, conditions. Later research by Keith Brewer, PhD and H.E. Sartori has shown that raising the pH range of a cell to 8.0 creates a deadly environment for cancer. The pH scale ranges from 0 to 14, with numbers below 7 representing an acidic condition and above 7 representing an alkaline, or oxygenated, condition. When cesium is taken up by cancer cells, it raises the pH of the cell. The cells that die are absorbed and eliminated by the body.
Cesium Chloride has been successfully used as an alternative or complementary cancer treatment for breast cancer, lung cancer, prostate cancer, colon cancer, pancreatic cancer, liver cancer, skin cancer, ovarian cancer, stomach cancer, cervical cancer, brain cancer, kidney cancer, testicular cancer, bone cancer, throat cancer, thyroid cancer, gastrointestinal cancer, cancers of the bladder and gallbladder, metastatic melanoma, and cancers in animals (including feline, canine, and equine cancer.)
It is extremely important when taking Cesium Chloride that one also supplement with Potassium!!
The Importance of Potassium in the Blood
Hyperkalemia is an excess of serum potassium. Most potassium in the body (98%) is found within cells; only a small amount usually circulates in the bloodstream [i.e. the serum]. The balance of potassium between the cells and the blood is critical to the body. It affects the way the cell membranes work and governs the action of the heart and the pathways between the brain and muscles. If you have excess potassium in the blood, it is usually excreted by the kidneys. However, the levels can get too high if your kidneys aren’t working right, which is the most common cause of hyperkalemia. Another cause is damaged cells releasing potassium into the bloodstream faster than even normal kidneys can clear it. Medications or diet may also affect the amount of potassium in the blood. Hyperkalemia is a serious condition that must be treated promptly.
Some patients on cesium develop evidence of potassium depletion so serum potassium needs to be monitored along with uric acid blood levels. Any alkaline therapy changes the pH of the body toward a more alkaline state. This causes movement of potassium into cells [i.e. which depletes serum potassium] which may result in low serum potassium values. In other words, cesium chloride does not drive potassium out of the cancer cells, rather it drives potassium into the cancer cells, thus reducing blood serum potassium levels. Potassium must be supplemented to the cancer diet to increase the amount of serum potassium. However, if the serum potassium get too high, then hyperkalemia can result. It is this delicate balance of serum potassium that forces a cancer patient to have their serum potassium level checked every couple of weeks. Kidney damage can result if serum potassium gets too high, but drinking higher levels of water generally takes care of this problem.
Symptoms of hypokalemia (too LITTLE serum potassium) include:
“… fatigue, muscle weakness and cramps, and intestinal paralysis, which may lead to bloating, constipation, and abdominal pain. Severe hypokalemia may result in muscular paralysis or abnormal heart rhythms (cardiac arrhythmias) that can be fatal.” http://lpi.oregonstate.edu/infocenter/minerals/potassium/index.html
Symptoms of hyperkalemia (too MUCH serum potassium) include:
“… tingling of the hands and feet, muscular weakness, and temporary paralysis. The most serious complication of hyperkalemia is the development of an abnormal heart rhythm (cardiac arrhythmia), which can lead to cardiac arrest.” http://lpi.oregonstate.edu/infocenter/minerals/potassium/index.html
In other words, both hypokalemia AND hyperkalemia can lead to muscular weakness and abnormal heart rhythm. While these are strong statements, getting your potassium level checked every 2 or 3 weeks should easily give you the ability to keep your potassium in a safe range (by making slight adjustments if your potassium levels get slightly above or slightly below the normal range).
HOW TO UTILIZE CESIUM CHLORIDE
Here is a summary of the rules for taking cesium chloride and potassium chloride:
Rule #1: Take 3 grams (i.e. 3,000 mg) of cesium cloride a day, divided into two equal doses of 1.5 grams each.
Rule #2: Take 1,200 mg of liquid ionic potassium chloride a day, divided into two equal doses. Note that the dose of potassium is less than half the cesium chloride dose, measured in milligrams (mg).
Rule #3: Take the potassium dose at least one hour after the cesium chloride. The reason for this is that if they are taken at the same time the potassium can block (i.e. compete with) the cesium chloride from getting into the cancer cells. The potassium should be taken orally.
Rule #4: Several of the foods you eat every day should be high in potassium. You should get more potassium from food intake than from potassium supplement. See the nutrient section for foods that contain potassium.
Rule #5: Drink lots of water with this treatment. It would be best to drink more than half a gallon of water a day for adults over 125 pounds.
Rule #6: Have at least two people do the calculations for how many TEAspoons or TABLEspoons of cesium chloride and potassium you take for each dose. Many people do not do the calculations correctly and take the wrong doses. Have a second pair of eyes read these instructions several times to make sure the doses are correct!! These are potent minerals that you are taking. An extreme overdose could kill you! PLEASE take this seriously!
In addition, you should add liquid ionic calcium chloride and liquid ionic magnesium chloride (or magnesium citrate) to your treatment.
Note: Some vendors of cesium chloride recommend 3,000 mg of liquid ionic potassium chloride per day and they do not mention having an hour gap between taking the cesium chloride and the potassium chloride. They may also have a person take the cesium chloride on a cycle of 5 days on, then 2 days off, or some other pattern. These instructions do not seem to be as effective as the above instructions.
Using DMSO With Cesium Chloride
DMSO is always required when you take cesium chloride. It is important to understand how to take them together. The recommended DMSO is 99.9% pure DMSO mixed: 70% DMSO and 30% distilled water or aloe.
First, Mix the DMSO and the cesium chloride together. The dosage of DMSO is one TABLEspoon each time you take the TABLEspoon of cesium chloride. DMSO is 100% natural and non-toxic. It should be noted that the FDA requires vendors to sell and label DMSO as a “solvent.”
AFTER they are mixed together, wait several minutes before you apply the mixture to the skin. Do NOT mix the potassium in with this mixture. As mentioned above the potassium should be given no less than one hour AFTER the cesium chloride.
You can use a spray bottle or eye dropper bottle to administer the liquid to the skin. SPREAD the mixture over a wide area of the skin. Otherwise you could get a rash.
While DMSO is non-toxic, it can be mildly dangerous to handle, so it is absolutely critical to read this article which covers the safety warnings about using DMSO (e.g. it should NOT be used by pregnant women or women who might be pregnant, it should not touch cloth or gloves, etc. – see the article):
A Word About Body Odor and DMSO
The 1 tablespoon of DMSO, twice a day (i.e. 2 tablespoons a day), may cause significant body odor. This body odor has been described as an oyster or garlic smell. The bad breath and/or body odor is caused by the DMSO leaving your body after doing its job. Normally it leaves via the kidneys, but sometimes it leaves through the skin. You may find yourself taking a shower and changing clothes more than once a day. But DMSO is absolutely critical to your treatment because it grabs hold of the cesium chloride and drives it through the skin and into the cancer cells. For brain cancer patients, it blasts past the blood-brain barrier like it wasn’t even there. Some cancer patients would rather die than have that much body odor. For advanced patients, that may explain their options.
What NOT To Take With Cesium Chloride
The above doses are designed to maximize the safe number of cancer cells that can be killed when treating cancer at home. NO alternative cancer treatment should be used with the cesium chloride and DMSO treatment that kills cancer cells. Killing too many cancer cells by combining treatments may lead to too much debris (i.e. dead cancer cells) in the body. This may cause an overload of toxins and congestion in the detoxification channels of the body. This is also why it is CRUCIAL that effective detoxification therapy be administered alongside Cesium Chloride therapy.
What CAN be added to this treatment are treatments that build nutrition, build the immunity system, protect the kidneys and liver, etc.
The Pattern of Taking the Cesium Chloride and Potassium
The Cesium Chloride should be taken EVERY DAY until you reach your cesium limit (which will be discussed below).
It is important to note that with the cesium chloride treatment tumors may actually become enlarged BEFORE they start to shrink. The reason is generally inflammation, which will be discussed below. For certain types of cancers this inflammation may create a dangerous situation and the dosage of cesium chloride may need to be reduced for a short time. But generally, it should be taken every day.
Warning #1: When the cancer patient reaches their cesium limit (which will be discussed below) the patient SHOULD CONTINUE TO TAKE POTASSIUM FOR ANOTHER 3 MONTHS!! The reason for this is that the cesium will stay in your body (and continue to pull potassium into the cancer cells and out of the blood serum) for about 3 months after you stop taking it.
Warning #2: If you have cancer anywhere in your digestive tract, and if your digestive tract is obstructed, do NOT take this treatment. As mentioned above, inflammation may result temporarily from this treatment, and inflammation added to an obstructed digestive tract can be very dangerous.
Please be sure to obtain more information regarding this treatment before trying it! If possible, I recommend finding an experienced alternative health practictioner to administer this treatment. However, many have reportedly been successful at administering this therapy on their own. Many cancers have reportedly been cured with this method; however, if this therapy is improperly administered, cesium chloride can be dangerous, even fatal. If done properly however, you could become cancer-free in a matter of days.
Items You’ll Need:
You must also administer detoxification therapy!!
How It Works:
Cesium has been proven to get into cancer cells. The cesium:
1) Makes the cancer cells alkaline (Note: the BLOOD is NOT made alkaline, only the inside of the cancer cells)
2) Limits the intake of glucose into the cell (thus starving the cell and making the cell “sick” from lack of food)
3) Neutralizes the lactic acid (which is actually what causes the cell to multiply uncontrollably)
4) Stops the fermentation process, which is a second affect of limiting the glucose.
One practitioner who used cesium chloride therapy was Hans A. Nieper, M.D., (1928-1998), who practiced in Hannover, Germany. Many celebrities and executives from America went to Germany to be treated by Dr. Nieper, including one President of the United States.
Cesium chloride works by making cancer cells highly alkaline, typically 8.0 and above, thus killing the cancer cell. Cesium chloride not only kills cancer cells, directly or indirectly, it immediately stops the metastasis of the cancer, can start shrinking tumor masses within weeks, and almost always stops the pain of cancer within 24 to 48 hours, depending on what is causing the pain.
Note that it is the CANCER CELLS, not the blood serum, that rises to 8.0 or above. The body keeps the blood serum within a small range of pH, around 7.4.
The Cesium Chloride Protocol directly targets cancer cells. Normal cells do not injest the cesium chloride. DMSO allows cesium chloride to target the cancer cells in an even more dramatic way.
Review the following sources for further information:
The High pH Therapy for Cancer
Tests on Mice and Humans
A. KEITH BREWER, Ph.D.
A.. Keith Brewer Science Library,
325 N. Central Ave., Richland Center, WI 53581
Reprinted from Pharmacology Biochemistry & Behavior, v. 21, Suppl., 1, by A. Keith Brewer, Ph.D., “The High pH Therapy for Cancer, Tests on Mice and Humans,” pp. 1-5, Copyright 1984, with permission from Elsevier Science. Single copies of the article can be downloaded and printed for the reader’s personal research and study.
BREWER, A. K. The high pH therapy for cancer tests on mice and humans. PHARMACOL BIOCHEM BEHAV 21: Suppl. 1, 1-5. 1984.—Mass spectrographic and isotope studies have shown that potassium, rubidium, and especially cesium are most efficiently taken up by cancer cells. This uptake was enhanced by Vitamins A and C as well as salts of zinc and selenium. The quantity of cesium taken up was sufficient to raise the cell to the 8 pH range. Where cell mitosis ceases and the life of the cell is short. Tests on mice fed cesium and rubidium showed marked shrinkage in the tumor masses within 2 weeks. In addition, the mice showed none of the side effects of cancer. Tests have been carried out on over 30 humans. In each case the tumor masses disappeared. Also all pains and effects associated with cancer disappeared within 12 to 36 hr; the more chemotherapy and morphine the patient had taken, the longer the withdrawal period. Studies of the food intake in areas where the incidences of cancer are very low showed that it met the requirements for the high pH therapy.
Cancer therapy…..Cesium…..High pH…..Pain…..Potassium…..Rubidium…..Tumor…..Vitamins
THE High pH Therapy for cancer was arrived at from an extensive series of physical experiments. These involved the isotope effect across membranes of many types, normal plant and animal, embryonic, cancer, and synthetic. It also involved mass spectrographic analyses of membranes and cells, as well as fluorescence and phosphorescence decay studies of many types of cells and parts thereof. It is the thesis of this paper that the results obtained throw a direct light upon the mechanism of carcinogenesis, and also indicate a therapy. Tests on both mice and humans substantiate this theoretical approach [1-8].
The isotope effect throws a very direct light on the mechanism of carcinogenesis. In this study it was shown that the 39K/41 Kratio in ocean water down to 6000 ft was 14,20000 [9-11].
In normal matured cells, both plant and animal, the ratio varied from 14.25 to 14.21. Embryonic and cancer cells all gave a ratio of 14.35. In the case of all synthetic cells across which there was a potential gradient, the ratio was 14.35. From these values it will be seen that the ratio in normal living cells indicates that as many isotopes leave the cell as enter.
In the case of potassium for embryonic and cancer cells as well as synthetic type cells with all types of membranes even including liquid mercury films the observed isotope ratio was given by equation 1.
(39K/ 41K ) o = (39K/41 K) n (41 + m / 39 + m) 1/2 (1)
where n refers to the normal ratio, o to the observed ratio, and m is the associated mass for the ions.
All cations in solution are associated. The attached mass for Cs+ is 3 molecules of water, for Rb+ it is 5 molecules, for K+ is 7 molecules. For cations below potassium in the Electromotive Series all ions are highly associated. This is to be expected from their position in the Hoffmeister Series. In the case of Ca++ the association is 30 molecules, while Na+ is 16. Equation (1) holds for all cations tested from H+to U+. The value of m however will vary when polar molecules are present in the solution. For example, K+ can also attach glucose. In contrast, Ca++ can attach a wide variety of molecules; it is this cation that transports peroxides into the cell, as well as metabolic products out of the cell.
The results given in equation (1) are most significant in that they show that transport is dependent entirely upon the frequency with which the ions strike the membrane surface. It is not a matter of capillary action, but one on which the ion and its associated mass pass directly through the bonding space between molecules which comprise the membrane. That the associated molecules are not lost in this transport is due to the fact that the attraction between the molecules and the ion is far greater than their attraction by the material of the membrane.
In the case of potassium an exact similarity exists between embryonic and cancer cells. The isotope ratio indicates that the K+ ions are taken up by the most efficient process possible. The same held true for Cs+ and Rb+.
In contrast to the above, a vast difference exists for cations below potassium in the EMS. In the case of embryonic cells all cations tested obeyed equation (1). In the case of cancer cells cations below potassium were taken up sparingly, if at all. For example the amount of calcium in cancer cells is only about one percent of that in normal cells .
The above isotope effect for potassium which transports glucose into the cell, and for calcium which transports oxygen are most significant with respect to Cancer. They mean that glucose can readily enter cancer cells but that oxygen cannot enter. This accounts for the anaerobic state of cancer cells pointed out by Warburg as early as 1925 .>
The mechanism responsible for the similarity in the isotope effect for potassium and rubidium in cancer and embryonic cells and for their marked difference in case of calcium was investigated in some detail using mass spectrographic analyses, and also fluorescence and phosphorescence decay patterns.
The phosphorescence decay patterns were found to be peculiar to and specific for all cell types or parts thereof [12-15]. It should be mentioned that the decay spectra is due entirely to the light emitted from the energized double bonds. All double bonds are capable of being raised to the energized state. While the fluorescence spectra and the phosphorescence decay patterns are both specific for each double bond they can be influenced by adjacent strong polar radicals. Again, both can be completely depressed by molecules absorbed over the surface; thus morphine, as well as attached polycyclic type molecules, will completely depress the excitation of the P=O radicals which characterize all cell membrane surfaces.
It was observed that the membranes tested gave a phosphorescence decay pattern due almost entirely to the P=O radicals which are composed of phospholipids. These radicals are specifically oriented over each type of membrane. This is most significant from the point of view of membrane action, since the P=O radicals are moderately strong electron donors in the ground state and strong to powerful donors in the energized state. This is due to the fact that the ionization potentials, 1st to 5th, are appreciably higher for the 0 than the P atom. This means that the 4 bonding electron orbitals will be displaced nearer the 0 atom thus surrounding this atom with a pronounced negative field. The P atom is thus positive in nature.
The above results are most important with respect to membrane action. They show that the strong electron acceptors Cs+, Rb+, and K+ can be attracted into the membrane so that they will enter the negative potential gradient which exists across all living membranes. In contrast to these cations, the highly associated cations farther down in the EMS are not sufficiently strong electron acceptors to be drawn into this gradient except when the P=O radicals are in the energized state. This means that K+ cations which transport glucose into the cell can readily enter cancer cells, but that Ca++ ions which transport oxygen into the cell cannot enter. In the normal cell the glucose, upon entering the cell, reacts with the oxygen in the cell and is burned to carbon dioxide and water with the liberation of heat. This heat in turn is absorbed on the membrane surface and raises the P=O radicals to an energized state which permits them to attach more Ca++ ions. Thus it will be seen that the amount of oxygen entering the cell is determined by oxidation within the cell, primarily that of glucose. This action is responsible for the pH control mechanism of the cell which maintains a value near 7.35.
The reactivity of the double bond has been studied in some detail using both light absorption and electron impact. It was found that energy states of the order of those produced by metabolic processes were not reactive. In contrast, high energy states such as those that are induced by radioactivity. are very reactive. Intermediate energy states in the ultra violet range were not reactive. Intermediate energy states in the ultra violet range were not reactive by electron impact, but slightly with light quanta. Here however the reactivity increased with a high power of the energy intensity per unit area . This suggests that the reactivity may be due to the multiple absorption of light quanta, thus raising the energy of the bond to the sum of the quanta absorbed (see Table 1).
THE MECHANISM OF CARCINOGENESIS
The experimental information presented in the previous section involving the isotope effect, mass spectrographic analyses, and fluorescence and phosphorescence decay, combined with the pH data supplied by Von Ardenne [23-25], makes it possible to define the mechanism involved in carcinogenesis. This mechanism is very different from the accepted one of carcinogens entering the cell and becoming attached to the DNA. This mechanism will not explain any of the experimental data outlined briefly herein.
The proposed mechanism can be outlined in four steps.
The attachment of carcinogenic type molecules to the membrane surface. This involves two factors: (a) the presence of carcinogenic-type molecules primarily of the polycyclic type, and (b) an energized state of the membrane, which may result from prolonged irritation. When these molecules are attached to the membrane glucose can still enter the cell, but oxygen cannot. The cell thus becomes anaerobic.
In the absence of oxygen, the glucose undergoes fermentation to lactic acid. The cell pH then drops to 7 and finally down to 6.5.
In the acid medium the DNA loses its positive and negative radical sequence. In addition, the amino acids entering the cell are changed. As a consequence, the RNA is changed and the cell completely loses its control mechanism. Chromosomal aberrations may occur.
In the acid medium the various cell enzymes are completely changed. Von Ardenne has shown that lysosomal enzymes are changed into very toxic compounds. These toxins kill the cells in the main body of the tumor mass. A tumor therefore consists of a thin layer of rapidly growing cells surrounding the dead mass . The acid toxins leak out from the tumor mass and poison the host. They thus give rise to the pains generally associated with cancer. They can also act as carcinogens.
HIGH AND LOW pH THERAPIES
Only two therapies will be mentioned here. Both are apparently effective. These are the Low pH therapy devised by Von Ardenne et al. [23-25] and the High pH therapy developed by the writer.
The Low pH Therapy
In this therapy devised by Von Ardenne, glucose is injected into the blood stream. As a consequence, the cancer cell pH will drop eventually to the 5.5 range. The patient is then placed in a furnace heated to 104 degrees Fahrenheit for a matter of hr [23-25]. The older the patient, the fewer the number of hours. The patient is allowed to breathe cold air. Diathermy is also applied over the tumor area which, in the absence of a blood supply, will cause the temperature of the mass to rise to something over 106 degrees Fahrenheit. At these high temperatures and in the acid medium, the life of cancer cells is very short. The only drawback to the therapy is that a case of severe toxemia may result from the out-leakage of the acid toxins within the tumor masses [23-25].
The High pH Therapy
The ready uptake of cesium and rubidium by the cancer cells lead the writer to the High pH therapy. This consists of feeding the patient close to 6 g of CsCl or RbCl per day in conjunction with the administration of ascorbic and retionic acids, Vitamins C and A, which being weak acids, upon absorption by the tumor cells will enhance the negative potential gradient across the membrane, and also zinc and selenium salts which, when absorbed on the membrane surface, will act as broad and moderately strong electron donors. Both types of compounds have been shown in mice to drastically enhance the pickup for cesium and rubidium ions.
The toxic dose for CsCl is 135 g. The administration of 6 g per day therefore has no toxic effects. It is sufficient however to give rise to the pH in the cancer cells, bringing them up in a few days to the 8 or above where the life of the cell is short. In addition, the presence of Cs and Rb salts in the body fluids neutralizes the acid toxins leaking out of the tumor mass and renders them nontoxic.
TESTS OF THE HIGH pH THERAPY ON MICE AND HUMANS
The therapy has been tested and the results will be discussed briefly below.
Tests on Mice
The High pH therapy was first tested at American University in Washington, DC using mice. In these tests, 2 mm cubes of mammary tumors were implanted in the abdomens of mice and allowed to grow for 8 days. The mice were then
divided into two groups. Both groups were continued on mouse chow, but the test group was given 1.11 g of rubidium carbonate by mouth per day in aqueous solution. After 13 more days the controls were starting to die so all mice were sacrificed and the tumors removed and weighed. The tumors in the test animals weighed only one eleventh of those in the controls. In addition, the test animals were showing none of the adverse effects of having cancer .
Results similar to those mentioned above were obtained at Platteville, WI using CsCl. More recently, Platteville has studied intraperitoneal injection of cesium carbonate for mice with abdominal tumor implants with 97% curative effect.
Tests using intraperitoneal injections of CsCl were carried out by Messiha et al. . The results were most successful and showed a drastic shrinkage in the tumor masses.
Tests on Man
Many tests on humans have been carried out by H. Nieper in Hannover, Germany and by H. Sartori in Washington, DC as well as by a number of other physicians. On the whole, the results have been very satisfactory. It has been observed that all pains associated with cancer disappear within 12 to 24 hr, except in a very few cases where there was a morphine withdrawal problem that required a few more hours. In these tests 2 g doses of CsCl were administered three times per day after eating. In most cases 5 to 10 g of Vitamin C and 100,000 units of Vitamin A, along with 50 to 100 mg of zinc, were also administered. Both Nieper and Sartori were also administering nitrilosides in the form of laetrile. There are good reasons to believe that the laetrile may be more effective than the vitamins in enhancing the pickup of cesium by the cells.
In addition to the loss of pains, the physical results are a rapid shrinkage of the tumor masses. The material comprising the tumors is secreted as uric acid in the urine; the uric acid content of the urine increases many fold. About 50% of the patients were pronounced terminal, and were not able to work. Of these, a majority have gone back to work.
Two side effects have been observed in some of the patients. These are first nausea, and the second diarrhea. Both depend upon the general condition of the digestive tract. Nieper feels that nausea can be prevented by administering the cesium in a solution of sorbitol. The diarrhea may, to some extent, be affected by the Vitamin C.
Only one case history will be presented here. A woman with 2 hard tumor masses 8 to 10 cm in diameter, one on her thyroid and one on her chest, was given 3 to 6 months to live. She had been subjected to chemotherapy, but was discontinued because it weakened her. She was taking laetrile on her own. She was given a 50 g bottle of CsCl and was told to take 4 g per day. She reported her case a year later. Being very frightened she took the entire 50 g in one week. At the end of that time the tumor masses were very soft, so she obtained another 50 g of CsCl and took it in another week. By the end of that time she could not find the tumors, and two years later there was no sign of their return.
LOW INCIDENCE CANCER AREAS
There are a number of areas where the incidences of cancer are very low. Unfortunately, the food composition in these areas has never been analyzed. At the 1978 Stockholm Conference on Food and Cancer it was concluded that there is definitely a connection between the two, but since the relationship was not understood, no conclusions could be drawn . The food intake has been studied by the author as far as possible from the high pH point of view. The results found will be discussed for a number of low incidence areas.
The Hopi Indians of Arizona
The incidence of cancer among the Hopi Indians is 1 in 1000 as compared to 1 in 4 for the USA as a whole. Fortunately their food has been analyzed from the standpoint of nutritional values . In this study it was shown that the Hopi food runs higher in all the essential minerals than conventional foods. It is very high in potassium and exceptionally high in rubidium. Since the soil is volcanic it must also be very rich in cesium. These Indians live primarily on desert grown calico corn products. Instead of using baking soda they use the ash of chamisa leaves, a desert grown plant. The analyses of this ash showed it to be very rich in rubidium. The Indians also eat many fruits, especially apricots, per day. They always eat the kernels. The results indicate clearly that the Hopi food meets the requirements for the High pH therapy.
The Pueblo Indians of Arizona
Some 20 years ago the incidence of cancer among the Pueblo Indians was the same as that for the Hopi Indians, since their food was essentially the same. But unlike the Hopi, these Indians have accrued certain items from outside their environment, hence supermarkets were installed in the area. Today the incidence of cancer among the Pueblos is 1 in 4, the same as the U.S. It is reported that there is a regular epidemic of cancer among them. It must be emphasized here that the high incidence of cancer is not due to what is in the supermarket foods, hut rather to what is not in it. It is essentially lacking rubidium and cesium and low in potassium.
The Hunza of North Pakistan
Cancer is essentially unknown among the Hunza, but unfortunately their food has never been analyzed. Talks with Hunza themselves and with Hindu professors who have spent some time in the area, have thrown sufficient light upon the food intake to show that it meets the requirements of the High pH therapy. They are essentially vegetarians, and are great fruit eaters, eating ordinarily 40 apricots per day; they always eat the kernels, either directly or as a meal. They drink at least 4 liters of mineral spring waters which abound in the area. Fortunately this water has been analyzed and found to be very rich in cesium. Since the soil is volcanic in nature, it must be concluded that it will be rich in Cs and Rb, as well as K.
Central and South America
The Indians who live in Central America and on the highland of Peru and Equador have very low incidences of cancer. The soil in these areas is volcanic. Fruit from the areas has been obtained and analyzed for rubidium and cesium and found to run very high in both elements. Cases have been reliably reported where people with advance inoperable cancer have gone to live with these Indians, and found that all tumor masses disappear within a very few months. Clearly the food there meets the high pH requirements.
In conclusion, the High pH therapy, as has been pointed out, was arrived at from physical experiments carried out on cancer and normal cells. It has been tested and found effective on cancers in both mice and humans. There can be no question that Cs and Rb salts, when present in the adjacent fluids, the pH of cancer cells will rise to the point where the life of the cell is short, and that they will also neutralize the acid toxins formed in the tumor mass and render them nontoxic.
Cesium Dosage and Side Effects
Several problems have arisen in the therapy which require further study. One of these is to determine the minimal dosage of CsCl that will kill cancer cells. Would cesium carbonate be better? Related to this are the effectiveness of intravenous injections, and, in certain cases, intraperitoneal injections. Both have been found to be effective in mice, but they have not yet been tested on humans.
The minimal dosage for curative action has not been determined. It has been observed by several physicians that the administration of 0.5 g per day of CsCl will actually enhance the rate of tumor growth. This is to be expected, since this low amount is sufficient only to raise the cell pH into the high mitosis range (see Chart 1). The data so far reveal that any quantity of 3.0 g or above will be effective.
A side effect which occurs in some cases, especially those who have had stomach ulcers, is nausea. This is far smaller for 3.0 g per day than for 6 to 10 g. The nausea can be minimized by administering cesium salt in a sorbitol solution as mentioned earlier. Further studies are necessary.
A limited number of patients have experienced diarrhea. Since cesium is a nerve stimulant , this can be expected. The effect is enhanced by taking large doses of Vitamin C, but it apparently is lowered by laetrile.
A further study is being made to determine the amount of cesium, rubidium or possible potassium in the diet that is sufficient to prevent cancer. Some data is available on the food composition in areas of the world where cancer is very low, but it is difficult to quantify, since the amount eaten varies greatly between individuals.
The effectiveness of potassium salts is yet to be determined. Tests to date have not been made on leukemia patients.
CESIUM BIOLOGICAL USES
In addition to the cancer therapy outlined in this paper, a  U.S. Patent has been issued on the use of cesium chloride as a nerve stimulant. Cesium salts are very effective in regulating heart arrhythmia. In areas of the world where cesium in the food intake is high, it has been noted that longevity of well over 100 years is not at all uncommon. Based on experimental data available  Cs salts may be useful in the treatment of manic-depressives.
In later writing, Dr. Brewer wrote: “The goal of the high pH therapy is the transport of large quantities of Cs+ Rb+ and glucose-free K+ across the membranes of cancer cells. During high pH therapy, Dr. H. Nieper, M.D., observed a loss of potassium which should be replaced.” Two booklets discussing Dr. Brewer’s final theories about cesium are available from the Brewer Science Library: “High pH Cancer Therapy with Cesium,” and “Cancer Its Nature and a Proposed Treatment,” both by A. Keith Brewer, Ph.D.
DISCLAIMER: The information contained on this website has not been evaluated by the Food & Drug Administration. It is not meant to diagnose, treat, cure or prevent any disease. Individuals suffering from any disease or illness should consult with a physician or health care professional. The Brewer Science Library offers Dr. Brewer’s writings for information purposes only and will assume no responsibility or liability for the use of any of the information we offer whether written by Dr. Brewer or others.
1. Brewer, A. K. The mechanism of carcinogenesis: Comments on therapy. J Int Acad Prev Med 5: 29-53, 1979.
2. Brewer, A. K. Cancer: Comments on the physics involved. Am Lab 5: 12-23. 1973.
3. Brewer, A. K., B. J. Clarke, M. Greenberg and N. Rothkopf. The effects of rubidium on mammary tumor growth in C57BL K/6J mice. Cytobios 24: 99-101, 1979.
4. Brewer, A. K. and R. Passwater. Physics of the cell membrane. I. The role of the double bond energy states. Am Lab 6: 59-72, 1974,
5. Brewer, A. K. and R. Passwater. Physics of the cell membrane. II. Fluorescence and phosphorescence in cell analysis. Am Lab 6: 19-29, 1974.
6. Brewer, A. K. and R. Passwater. Physics of the cell membrane. III. The mechanism of nerve action. Am Lab 6: 49-62, 1974.
7. Brewer, A. K. and R. Passwater. Physics of the cell membrane. IV. Further comments on the role of the double-bond. Am Lab 7: 41-50, 1975.
8. Brewer, A. K. and R. Passwater. Physics of the cell membrane. V. Mechanisms involved in cancer. Am Lab 8: 37-45, 1976.
9. Brewer, J. Isotopes of potassium. Ind Chem Eng 30: 893, 1938.
10. Brewer, J. Abundance of the isotopes of potassium in mineral and plant sources. J Am Chem Soc 58: 365-369, 1936.
11. Brewer, A. K. Man spectrographic analysis of the constancy of the atomic weight of potassium in ocean water. J Am Chem Soc 58: 370-375, 1936.
12. Brewer, A. K. Excitation of the hydrocarbon double bond. Am Sci 56: 259, 1968.
13. Brewer, A. K., S. Adelman, H. Hoerman and W. Sanborn. Differential identification of biological entities by phosphorescence decay. Nature 213: 718-719, 1976.
14. Brewer, A. K. and S. Adelman. Method for analysis and identification of biological entities by phosphorescence decay. U.S. Patent 3, 470, 373, 1969.
15. Brewer, A. K. Methods and means for the detection of microorganisms in the air. U.S. Patent 3, 566, 114, 1970.
16. Brewer, A. K. Chemical action in low volt arc. Physiol Rev 42: 785, 1932.
17. Calloway, D. R., R. D. Giaque and F. N. Costa. The superior mineral content of some American Indian food, in comparison to Federal donated counterpart commodities. Ecol Food Nutr 3: 203-210, 1974.
18. Editorial. Lancet 1: 1204, 1964.
19. Masco. H. L. U.S. Patent 3, 614, 242, 1972.
20. Messiha, F. S. The antidepressant action of cesium chloride and ethanol preference in rodents. In: Alcoholism: A Perspective. edited by F. S. Messiha and B. S. Tyner. New York: PJD Pub., 1980, pp. 247-259.
21. Messiha, F. S., A. El-Domeiri and H. F. Sproat. Effects of lithium and cesium salts on sarcoma-I implants in the mouse. Neurobehav Toxicol 1: 27-31, 1979.
22. Special report. Food and cancer. Nutr Rev 36: 313-314, 1978.
23. Von Ardenne M., P. G. Reitnauer and D. Schmidt. Theoretische Grundlagen und in vivo Messungen zur Optimierung der selekiven übersäurung von Krebsgewebe. Acta Biol Med Germ 22: 35-60, 1969.
24. Von Ardenne, M. Selective multiphase cancer therapy: Conceptual aspects and experimental basis. Adv Pharmacol Chemother 10: 339-380, 1972.
25. Von Ardenne, M. and A. Von Ardenne. Berechnung des pH-Profile im Interkapillarraum der Krebsgewebe für die Faelle mit und ohne Langzeit-Glucose- Infusion. Res Exp Med 171: 177-189, 1977.
26. Von Warburg, O. Metabolism of human tumor cells. Klin Wohnschr 4: 2396-2397, 1925
- You must be logged in to reply to this topic.