There has been a lot of talk about cesium chloride for the treatment of cancer. I have not seen any proof of effectiveness, and no talk about the dangers, including death. So I am going to address these here. As for effectiveness it has been claimed to be highly effective against all cancers. So how do they explain this study?
Zero efficacy with cesium chloride self-treatment for brain cancer
Samadani U, Marcotte P. Mayo Clin Proc. 2004 Dec;79(12):1588
Safety is also a big concern as the side effects can not only be very dangerous, but deaths have been reported as well.
http://www.ncbi.nlm.nih.gov/pubmed/18657021?ordinalpos=2&itool=EntrezSyst...
Cesium-induced QT-interval prolongation in an adolescent.
Pharmacotherapy. 2008 Aug;28(8):1059-65.
http://www.ncbi.nlm.nih.gov/pubmed/15301336?ordinalpos=12&itool=EntrezSys...
Acquired long QT syndrome and monomorphic ventricular tachycardia after alternative treatment with cesium chloride for brain cancer.
Mayo Clin Proc. 2004 Aug;79(8):1065-9.
http://www.ncbi.nlm.nih.gov/pubmed/12958400?ordinalpos=20&itool=EntrezSys...
Blood and tissue concentration of cesium after exposure to cesium chloride: a report of two cases.
Biol Trace Elem Res... 2003 Aug;94(2):97-104
RESULTS: High levels of cesium were found in brain, liver, kidney, bile, gastric content, and whole blood collected at autopsy as compared to reference levels. The administration of cesium chloride resulted in blood levels a factor of 1100 higher than normal. The highest Cs concentrations were found in the liver (1029 microg/g, dry wt), followed by the kidney (815 microg/g, dry wt) and brain (219 microg/g, dry wt). CONCLUSION: The high accumulation in the liver suggests that hepatotoxicity from Cs might be an initial presenting symptom in Cs-poisoning cases. This is the first report describing two cases with high Cs levels in human tissues.
http://www.ncbi.nlm.nih.gov/pubmed/12548155?ordinalpos=24&itool=EntrezSys...
Cesium toxicity: a case of self-treatment by alternate therapy gone awry.
“Cesium salts have been used in animal models to induce cardiac arrhythmias for several decades, but the sequelae of human cesium toxicity have seldom been described. The authors describe a case of cesium toxicity manifested by syncope, polymorphic ventricular tachycardia, hypokalemia, and a QT interval prolonged to 650 milliseconds that resolved over 4 days following withdrawal of cesium. The patient had a 2-year history of colon cancer and had self-treated with cesium chloride, 3 g/d, for several weeks, using cesium as a form of alternate therapy for cancer. The authors describe the pathophysiologic correlates and risks of cesium consumption and conclude that cesium toxicity should be considered among the differential diagnoses of prolonged QT interval.”
http://www.ncbi.nlm.nih.gov/pubmed/17212573?ordinalpos=7&itool=EntrezSyst...
Acquired long QT syndrome secondary to cesium chloride supplement.
“The use of complementary medication is on the rise worldwide. More often than not, the treating physicians are unaware of this and also unfamiliar with the potential benefit or toxicity of the agents. Here, we present the case of a 39-year-old woman who presented with new onset of syncope as a result of acquired long QT syndrome secondary to taking a cesium chloride supplement. A brief discussion of the pathophysiology of this agent follows the case presentation.”
http://www.ncbi.nlm.nih.gov/pubmed/10826508?ordinalpos=14&itool=EntrezSys...
Cesium chloride induced ventricular arrhythmias in dogs: three dimensional activation patters and their relation to the cesium dose applied.
http://www.ncbi.nlm.nih.gov/pubmed/9786077?ordinalpos=16&itool=EntrezSyst...
Cesium-induced atrial tachycardia degenerating into atrial fibrillation in dogs: atrial torsades de pointes?
http://www.ncbi.nlm.nih.gov/pubmed/9321828?ordinalpos=19&itool=EntrezSyst...
Three-dimensional activation sequence of cesium-induced ventricular arrhythmias.
http://www.ncbi.nlm.nih.gov/pubmed/1427509?ordinalpos=25&itool=EntrezSyst...
Relative protection given by extract of Phyllanthus emblica fruit and an equivelant amount of vitamin C against known clastogen—caesium chloride
Aqueous extracts of Phyllanthus emblica L. fruit and an equivalent amount of vitamin C were administered orally by gavage to laboratory-bred Swiss albino mice for 7 days in order to evaluate the protection afforded by the two extracts against clastogenic effects of different doses of caesium chloride (CsCl) on bone marrow cells of Mus musculus in vivo. Both pretreatments significantly reduced the frequency of chromosome aberrations induced by CsCl given at three different doses, indicating that vitamin C, an essential component of P. emblica extract, was the effective agent in protecting against the clastogenicity of the metal salt.
The reason that they have to prevent clastogenicity of cesium chloride is because clastogencity refers to breakage of chromosomes. This is one of the contributing factors to the formation or cell damage and cancer.
http://www.ncbi.nlm.nih.gov/pubmed/2048156?ordinalpos=28&itool=EntrezSyst...
Inhibition of clastogenic effects of cesium chloride in mice in vivo by chlorophyllin.
“The antagonistic effect of chlorophyllin was tested in reducing the clastogenic action of cesium chloride (CsCl) in vivo on mice bone marrow cells. CsCl induced chromosomal aberration in frequencies directly proportional to the dose administered. Chlorophyllin, when given alone, was not clastogenic even at a concentration of 1.5 mg/kg body wt. of the animal. Simultaneous administration of chlorophyllin and CsCl reduced chromosomal aberrations significantly at 24 h. Exposure to the same dose of chlorophyllin 2 h before exposure to CsCl also decreased clastogenic effects but to a lesser extent. These findings are of importance in view of the uptake of radioactive Cs by green plants after nuclear fallout.”
http://www.ncbi.nlm.nih.gov/pubmed/1931434?ordinalpos=29&itool=EntrezSyst...
Comparative efficacy of chlorophyllin in reducing cytotoxicity of some heavy metals.
“The potential of chlorophyllin in reducing clastogenicity was studied against two concentrations of each of three potent metallic clastogens (cesium chloride, mercuric chloride and cobalt chloride) in bone marrow cells of mice in vivo. The respective salts and chlorophyllin were administered orally to mice by gavaging in different combinations. Simultaneous administration of chlorophyllin with both concentrations of each salt reduced the clastogenic effects in the order Cs greater than Hg greater than Co. Chlorophyllin could not decrease the clastogenic effects when administered 2 h before the salts.”
http://www.ncbi.nlm.nih.gov/pubmed/9438035?ordinalpos=26&itool=EntrezSyst...
Modification of cesium toxicity by calcium in mammalian system.
“The interaction between cesium chloride CsCl and calcium chloride CaCl2 was observed in bone marrow chromosomes of mice. The two salts were administered orally to laboratory bred Swiss albino mice in vivo singly or one followed by the other, or both simultaneously. CsCl induced chromosomal aberrations in frequencies directly proportional to the dose administered. The frequency of aberrations was reduced significantly when the two chemicals were administered simultaneously or when CaCl2 was given 2 h before CsCl. Thus, CaCl2 is able to protect against the cytotoxicity of CsCl.”
http://www.ncbi.nlm.nih.gov/pubmed/1879407?ordinalpos=30&itool=EntrezSyst...
Cytogenetic damage induced in vivo to mice by single exposure to cesium chloride.
“Female laboratory bred albino mice (2n = 40) were orally administered cesium chloride (CsCl) in aqueous solution as a single dose and the damage induced at the chromosomal level was observed in bone marrow cells after 6, 12, 18, and 24 hours of exposure. The concentrations of the chemical given were calculated as fractions of the LD50, namely 1/5, 1/10, and 1/20. The cytogenetic endpoints screened for were chromosomal aberrations (CA) and divisional frequency or mitotic index (MI). The frequency of chromosomal aberrations induced was directly proportional to the concentration of the chemical administered. The highest dose was the most toxic and was considered to be the maximum tolerance level. Effects on divisional frequency were variable, the highest concentration being significantly mitostatic, the middle one ineffective, and the lowest slightly mitogenic. In general, the observations indicate that CsCl is clastogenic when administered orally to mice in vivo and the effects are dose-dependent.”
http://www.ncbi.nlm.nih.gov/pubmed/2385244?ordinalpos=31&itool=EntrezSyst...
Clastogenic effects of cesium chloride on mouse bone marrow cells in vivo.
“Clastogenic effects of cesium chloride (CsCl) on mouse bone marrow cells in vivo following oral administration were studied after 24 h. The incidence of chromosome aberrations increased linearly with increasing concentrations of the chemical from 1/20th to 1/5th of the LD50. The frequency of cell division was also enhanced by the lower doses but higher doses were mitostatic. This report is the first on the clastogenicity of cesium on animals.”
Note the quote “The frequency of cell division was also enhanced by the lower doses”. Last thing you should do with cancer is enhance cellular division, which is what cancer basically is. Cells dividing at an abnormally fast rate. Higher doses stop this division, but as we have seen from the other studies the toxicity of cesium increases with dose. Toxic reactions from cesium chloride use can include heart rhythm abnormalities and death.
http://www.ncbi.nlm.nih.gov/pubmed/1689430?ordinalpos=32&itool=EntrezSyst...
Early and delayed afterdepolarizations associated with cesium chloride-induced arrhythmias in the dog.
http://www.ncbi.nlm.nih.gov/pubmed/2611814?ordinalpos=33&itool=EntrezSyst...
Cardiovascular and metabolic effects of caesium chloride injection in dogs—limitations as a model for the long QT syndrome.
“The morphological features of these caesium induced ventricular tachyarrhythmias, their response to overdrive pacing, and their occurrence despite substantial hyperkalaemia are quite different from the properties of the clinical long QT syndrome, which is overdrive suppressible, favoured by hypokalaemia, and rarely degenerates to ventricular fibrillation.”
http://www.ncbi.nlm.nih.gov/pubmed/2813559?ordinalpos=34&itool=EntrezSyst...
A toxicology evaluation of postnatal maternal exposure to cesium.
“The effect of postnatal maternal exposure to CsCl on the newborn was studied in the mouse. Maternal ingestion of 1 mEq CsCl solution as the only drinking fluid began immediately after birth and the offspring were breast-fed until weaning. They were then separated from the nursing dams and remained Cs free for a subsequent 2 weeks prior to sacrifice. Maternal Cs exposure decreased the weanling body weight from controls and they attained normal body weight after 2 weeks of Cs-free period during development. Maternal Cs ingestion caused a reduction in offspring brain weight of both sexes compared to controls. The kidney weight of the developing female, but not male, offspring was also decreased from controls as a consequence of maternal Cs exposure. The offspring's hepatic alcohol and aldehyde dehydrogenase were not altered from controls as a function of maternal exposure to Cs salt. Little changes occurred in offspring heart lactate dehydrogenase by the maternal Cs treatment. The results suggest that maternal Cs exposure during breast-feeding affected body weight and the CNS of the offspring. The change noted in weanling kidney weight was sex dependent. These gross pathological changes in weanling organ weight were not apparent when maternal breast-feeding was eliminated. The data indicates that Cs adversely affected the newborn which was eliminated after cessation of the Cs exposure.”
http://www.ncbi.nlm.nih.gov/pubmed/3370776?ordinalpos=37&itool=EntrezSyst...
Magnesium suppression of early afterdepolarizations and ventricular tachyarrhythmias induced by cesium in dogs.
“Cesium induced sustained monomorphic ventricular tachycardia, torsades de pointes, or ventricular fibrillation in 12 of 13 dogs before magnesium infusion, and in eight of 11 dogs 1 to 2 hr after stopping infusion, but in only three of 13 dogs during magnesium infusion.”
For those not familiar with ventricular tachycardia, torsades de pointes, and ventricular fibrillation, these are VERY dangerous heart rhythm abnormalities.
http://www.ncbi.nlm.nih.gov/pubmed/6522431?ordinalpos=48&itool=EntrezSyst...
Effect of cesium and potassium salts on survival of rats bearing Novikoff hepatoma.
“Rats treated with CsCl for 12 consecutive days prior to or immediately after inoculation with 1.0 ml of viable hepatoma cell suspension showed an increase in mortality score from corresponding controls.”
http://www.ncbi.nlm.nih.gov/pubmed/6395134?ordinalpos=52&itool=EntrezSyst...
Effect of cesium and ethanol on tumor bearing rats.
“The results indicate potentiation of the hepatoma toxicity by CsCl which may be minimized by ethanol.”
Bottom line is that cesium chloride has not been demonstrated to have anti-cancer activity against all cancers as is being claimed. But study after study has shown a high potential for toxicity, especially on the heart, and possibly even death. There are so many safe treatments for cancer out there that I personally would avoid getting anywhere near this dangerous therapy.
I am glad they made some of the changes they did, such as eliminating silver chloride, but there are still a few things I am leery of.
DMSO can be a good thing if used carefully and properly. Though I generally do not recommend it due to the hassles and safety issues. My biggest concern is people not cleaning the application site properly. Because DMSO crosses the skin so rapidly it will also take pretty much anything it contacts through the skin with it in to the bloodstream. This includes soap scum. So the area needs to be cleaned really well with soap and water, then again with rubbing alcohol to remove the soap scum before applying the DMSO.
My other big concern is the possible reaction of the hypochlorite, improperly being referred to as chlorine dioxide (a very toxic gas), with the DMSO. This is based on the Ramirez case a while back in which there was a conversion of the DMSO a cancer patient was using in to toxic DMSO4. Here is a link to where I discussed it before:
http://www.curezone.org/forums/fm.asp?i=1435824#i
Anyway, hypochlorites are oxidizers, and there is not enough known about interactions between DMSO and oxidizers. We do know that we can oxidize DMSO with heat in to DMSO2, also known as methylsulfonylmethane (MSM), but not with stronger oxidizers.
Hypochlorites make me nervous anyway. Again very little is known about their action in the body or interactions with other compounds. Chlorine is needed by the body, but it also forms some of the most toxic compounds known to man such as nerve agents.
MSM is good, but I still prefer to get my sulfur from natural sources as much as possible. Commercial MSM is not natural. Again it is synthesized from the industrial solvent DMSO.
I had a lady one time selling MSM through network marketing try to convince me that MSM was natural. She said it came from trees. Actually the DMSO is a byproduct of the paper industry. This is then heated to convert the DMSO in to MSM. So I told her that is like claiming plastics are natural since they are formed from naturally occurring oil.
I have never been a big fan of colloidal silver either. I think it is way overhyped. And I have found that many of the silver products on the market are either not true colloids or contain very little silver. And they charge a fortune for something that literally takes pennies to make.
I have made strong colloidal silver solutions in the past but rarely did much with them. The last time I used it was about 15 years ago when I cut half of the last digit of my thumb off on a table saw. What was left of the cut off part was too mangled to put back on so I figured I was going to have to live with a short thumb the rest of my life. On a couple of tips (no pun intended) from a doctor friend of mine and some natural healers I combined their suggestions. The doctor showed me some nylon impregnated with silver that could be put over the amputated area and the silver driven in to the tissue with electrical energy to stimulate tissue growth on the amputation. He only had a tiny piece though about the size of dime. So I substituted a very concentrated colloidal silver solution that I would soak the amputation in. My other friends had mentioned regrowing amputated areas with high voltage through argon tubes. Keep in mind that the body is electric, and electricity has been shown to stimulate the growth of some tissues, such as bone. I was willing to try anything, so I looked for a tube. I could not find an argon tube, but I managed to scrounge a neon tube from a photospectrometer. I hooked that up to a 15,000 volt 30ma transformer. I would soak the amputated section in the silver then turn on the power and put the amputated silver soaked area up the tube with the 15,000 volts running through it to help drive the silver in (according to the hypothesis). First thing I noticed is that was a WONDERFUL pain killer. And it took 6 months, but I grew the entire tip of the thumb back. There is just a little, hardly noticeable scar, and I have only recovered about 90% of the feeling in the tip of the thumb. That I can care less about, I was just so grateful to have the rest of my thumb back!!!
Other than that I have ingested very little as I found it was not very effective for things like colds and flu. I have other things for that. And don't ask what because the most effective thing I found again is not safe unless you really know what you are doing. I did this once though with a cold and all my symptoms were gone within a minute. And talk about nasty tasting!!!
Silver nitrate is something that is best not fooled with. It can accumulate in tissues, and it can be poisonous.
This is not to say silver is bad. I do think it has its place. For instance silver nitrate had a long history of being used in the eyes of babies to prevent herpes induced blindness. And Silverdene is used to control infections on burns. It is just I will not use colloidal silver unless I make it myself so I know how much silver is in it and that it is a true colloid. Even at that I have other things I prefer in most cases such as herbs, ozone, and radiofrequency therapy.
I am going to cut this short and continue with another post so this does not get too long. Makes it harder to quote and respond when posts get too long.
They are right about being careful with killing cancer cells. There are ways for example to kill off large amounts of cancer cells. But this also comes with risks. If you killed off a basketball sized tumor in a single shot you would likely kill the patient from sepsis. We have to keep in mind that dead cells in the body are infectious material. The body has to have time to clear dead cells from the body before adding to the load by killing more cells.
One thing that I did not like was their saying not to use any antioxidants, immune builders or even multivitmains. Cancer patients need to protect their healthy cells from free radicals such as chemotherapy, radiation therapy and oxidizers. Many cancer patients also suffer from cachexia, and really need to maintain their nutrition. I have an old training textbook on cancer written for doctors. One thing I found really interesting in the book was their statement that most cancer patients do not die from their cancer. Instead, most cancer patients die from the malnutrition brought on in large part from their treatments. The treatments can cause severe nausea preventing them from getting all of the nutrition they really need.
They are partially right about the microbial connection to cancer. There are numerous viruses, bacteria, fungi, etc. capable of causing cancer. But these are not the only cause. DNA damage, from sources such as radiation exposure and other sources, can also cause cancer. By far though viruses are the number one cause of most cancers. There was a very interesting article back years ago in Discover magazine discussing oncogenes (genes that cause cancer). They finally admitted what had been known in medicine for decades but the medical establishment was doing their best to cover up. They made the simple statement that every oncogene that had been found to date was viral, and that no human oncogene had ever been found. The medical establishment wanted to keep this quiet because the implications were enormous. They would not only have to admit that they had known for a long time that cancers WERE NOT hereditary, which meant that they were knowingly conducting unnecessary testing on people because they had a family history of cancer. This would also leave major legal implications on doctors performing these unnecessary tests, but also for the doctors scaring women in to getting prophylactic mastectomies and men in to getting prophylactic prostectomies. What this means is that the doctors were convincing these women and men to have their HEALTHY tissues surgically removed to prevent the possible formation of cancer in these tissues in the future.
They also repeat the common myth that everyone has cancer cells and that our immune systems just fight them off. I think whoever started this myth was mistaking non-malignant tumor cells for malignant (cancerous cells). Even though they share some properties there are still very big differences. A simple way to prove this myth is with a little common sense. Everyone will suffer immune suppression at various times throughout their lives. Think about it. Why doesn't everyone get sick from let's say cold or flu viruses they are exposed to? If your immune system is intact and strong then your immunity can help fend off the infection. This is why we rarely see hospital personnel getting sick from the constant barrage of microbes they are exposed to. When your defenses are down you are more susceptible to these microbes. So if we all had cancer cells all the time the cancer cells would take hold, just like a cold or flu virus, when our defenses are down. And once they take hod they can further weaken our system. Therefore, if their claim was true then we should all have been dead a long time ago.
Another thing I disagree with is under their goal claim. They claim the goal is to kill every microbe in every cancer cell. Not all cancer cells contain microbes. First of all not all cancers are microbial in origin. As I mentioned earlier radiation is one thing that can cause DNA breakage. A few rare leukemias for example have been linked to DNA damage from radiation. Thyroid cancer is common around nuclear power plants, such as Hanford, where radioactive iodine has been released. Radon gas can lead to lung cancer.... Furthermore, it is only some cells that get infected with viruses leading to the cancer. These cells (mother cells) create an excess of cellular division hormones, known as trephones in Europe. When the level of trephones exceed the level of trephone inhibitors the excess trephones lead to a higher than normal level of abnormal cell (daughter cell) growth. This is the malignant tumor. The reason we develop chem resistant tumors is because mother cells are not destroyed by the chemo due to the extra genetic material they contain. The daughter cells are killed though since they do not contain the extra viral genetic material. So the cancer goes in to "remission" since the mass of mother cells is too small to be detected. When they grow though they create clones of themselves leading to the development of a chemo-resistant tumor. This is just a quick simplified explanation so I am not sitting here all night typing. Look in to the research of Gaston Naesson for pieces of what I just explained.
There are some other minor things I disagree with. My biggest problem with this protocol is a lack of any evidence of efficacy or even a demonstration that it really reverts cancer cells to normal. I also have a problem with the mixture since it is unknown how these different chemicals are going to interact with each other. For example will the colloidal silver react with the DMSO or MSM forming silver sulfate, or with the sodium chlorite and hypochlorite (the breakdown products of the highly unstable chlorine dioxide) forming toxic silver chloride? Just too many safety issues to be answered.
I also have to admit that it really bothers me that they keep referring to the MMS as chlorine dioxide when it is not chlorine dioxide. Chlorine dioxide is a toxic and unstable gas. It reacts with water yielding the sodium chlorite and hypochlorite. I have a problem with companies repeatedly making misleading claims, especially when they have been told over and over that the claim is misleading. Do they feel that chlorine dioxide somehow sounds more healthy or scientific? Or are they trying to distance themselves from the relationship of MMS to common household bleach? Regardless of the reason, being deliberately misleading is being deliberately misleading. And this makes me wonder what else they are being misleading about in order to sell product. Network marketing companies are notorious for making up false claims about their products, hyping them up to justify the ridiculous prices. And I cannot stand networking marketing companies for this reason. So when I see MMS promoters deliberately claiming that it is something it is not I am going to take ALL of their other claims with a grain of salt until I see some solid evidence to the contrary.
Boy are you keeping me busy with your post, LOL!!!
Finally I wanted to address their claims about Rife. I love Rife units provided they are not the all fluff ones. What I mean by this is the ones that have all the different frequencies. I was introduced to Rife Technology about 18 years ago. I managed to get a hold of copies of lot of Rife's original papers and schematics for machine. I do not do electronic circuitry, so I had a custom unit built for me. The first unit was a mix of radio tubes and solid state, and had 7 frequencies. I used alligator clips attached to paper towels soaked in saline for the conduction. The next generation had 6 frequencies, and used independent foot baths with salt. The next generation pretty much the same, but with molded foot baths. After that 3 more frequencies were dropped leaving the 3 frequencies Rife kept. He did not have an 11 page frequency list as is going around. More on that later. The newest generation is a single fixed frequency and no foot bath. Instead is has a metal plate that you put your fingers on and the frequency is "broadcast" through the body.
Before anyone asks, NO, I don't sell them, and I do not have access to any for sale. All of these were prototypes, many of which I lent out to people with illnesses.
All of the units were built strictly for research purposes. This is why frequencies kept getting dropped. Again, I know this is going to open up a can of worms, but Rife only kept 3 frequencies. He did not have hundreds of frequencies as some have claimed. The 11 page frequency list going around is bogus. In fact if you look at some of the frequencies they include dangerous ones such as 42hz, which is the frequency of formaldehyde, which is a carcinogen. So why they are listing that as an anti-cancer frequency is beyond me. We think that a lot of the bogus frequencies were put out there by Rife's second partner Crane in order to throw people off of the real research since he was selling his units for a ridiculous $7,500 a piece. Superb results can be obtained from a single fixed frequency unit costing less than $100. Sellers like to add as many frequencies though to make their units APPEAR more high tech and effective to they can command higher prices. We have had some of these other units tested by an alternative practitionaer and found that they did not work as well as the simple one frequency units.
I am not very good about explaining this part, but there is a basis behind Rife's frequencies that even he did not understand. His machine was not curing people by blasting apart microbes, but rather by retuning the body back in to proper resonance.
This all came about after noticing that Rife's second and third frequencies were much slower to heal than his first frequency (666hz). Yes, I know!!! The 666 being the mark of the beast is Hollywood hype. The supposed real number for the mark of the beast is actually totally different. We also noticed a lot of things being successfully treated that had nothing to do with pathogens. Diabetic neuropathy, general pain, and nerve regeneration as examples.
So the builder started doing some calculations on the different frequencies and found a correlation between our primary frequency and and Rife's remaining 3 frequencies. The reason the last two were slower? Because they were each off by one. So we stuck to the 666hz and found that they worked for every disease and condition they were used for. This included various cancers including very advanced liver cancer, neuropathy, MS, chronic fatigue, nerve regeneration in the brain after surgical removal of tumors, fibromyalgia, etc.
This all brings me back to their claim that the Rife units cure the cancer within 24 hours by converting the cells back to normal by destroying the cancer pathogen. No, Rife units do not cure cancer within 24 hours. On average they take about 1 month. I found that if a person has had previous radiation therapy that it takes much longer. I believe this is because cancer cells can build up a tolerance to radiation therapy the same way they can build up a tolerance to chemotherapy. Both radiation therapy and Rife units use forms of electromagnetic radiation. So the cells building a tolerance to the radiation therapy are inadvertantly building a resistance to the Rife units as well. The longest I have ever seen these units take to get rid of cancer was in someone suffering from bone, esophageal, and lung cancer. He had previous radiation therapy, which did not eradicate the cancer. When he started on the Rife unit the cancer growth just stopped. It did not grown and it did not shrink. It just stayed static for about 6 months. Then it finally started shrinking. Two months later it was completely gone.
As an interesting related note, did you know that electrotherapy was actually started by the ancient Greeks? They used electric eels and rays to shock people with high voltage to cure various diseases. Modern medicine is still trying to catch up with what has been known for thousands of years.
Dr. Royal R. Rife published more than just 3 frequencies as stated. The following list comes directly from Rife's own lab notes: 1935 -1939. There were many other frequencies Dr. Rife used from 1934 and before as well. Some are listed below in Hertz. Here are Rife's frequencies from his notes:
I said Rife KEPT 3 frequencies. Of course he experimented with other frequencies.
What is your source that Dr. Rife only used 3 frequencies?
From copies of his original notes, not rewritten notes posted on the web.
I've never read this anywhere before... His lab notes have been publicly available for years. Where did you read in Rife's notes about the 666 Hz?
Again from copies of his original notes. I have copies of a lot of his original research that I have had long before the internet came available to the general public.
Also, one is going to need more power than a $100 CD system can provide.
Not true at all!!!! There is no reason for high power. If you understand how Rife units really work then you would understand why. Using high power is like using 10 aspirin when one will do. The power used is 12V or less, and I have seen these units work time after time. We have had alternative doctors test them with equal results. In fact one of the doctors in Norhtern California tested these units as well as other Rife units and said that these units worked better than any other Rife unit she had tested. So don't try to feed me that crap!
Rife himself used a carrier. Where is the mention of a carrier frequency to carry these low freqeuncies to the body. You aren't going to find it commercially available at that price.
The Rife units don't work the way he thought they did. We found that they were doing a lot of things that Rife's hypothesis could not explain. This was because they were working on a totally different principle than Rife thought they were working on.
What is your source, since you made said this can be done?
See above.
I've never read that it only takes 24 hour with a Rife generator to eradicate cancer? You have misquoted quite a bit throughout your posting. Please study the facts before you post!
You need to learn to read!!! I did not say that, I was quoting and contradicting the statement. Here is the quote again, pay attention this time:
"This all brings me back to their claim that the Rife units cure the cancer within 24 hours by converting the cells back to normal by destroying the cancer pathogen. No, Rife units do not cure cancer within 24 hours. "
The only reason I can think of why you would come here and act like such a jerk is because you are selling, or are somehow otherwise involved in selling overpriced and overhyped Rife units. Go elsewhere!