Cancer Regimen
This is what I would do if I had cancer.
SUMMARY - Use a wide spectrum antiseptic such as Eclectic Institute Para-Fight (formally known as Intestinal Support), plus vitamin D, whey protein, and non-acidic enzymes. These are the basics to use long term. 
Cancer - What I Would Do
For diet, control blood sugar levels by limiting grains and other starchy carbohydrates and sugars and getting adequate protein and good oils such as by the Zone Diet (see Diet section). Clean up the home environment and limit toxin absorption and ingestion (see Toxin Avoidance). Toxin avoidance can be a challenging part of a cancer regimen. Drink plenty of water as in the Water Cure.
Cancer should always be treated as a long term infection until it is gone. Never lose sight of this. Whether the infection is from fungus, bacteria, viruses, and/or parasites, one or more of these is probably directly or indirectly causing the problem. Any of these can produce growth factors, which are probably the key to understanding and controlling cancer, as well as indirectly affect the immune system such that it is less effective to fight cancer.
When people start researching various alternative treatments and getting advice from many people, they often end up using hundreds of dollars worth of supplements per month, some of which are only marginally if at all useful, mostly under the guise of "boosting the immune system." Usually, using antiseptic supplements are far more effective, especially considering that ridding the body of pathogens directly is the best immune system booster.
The cardinal rule of effective complementary cancer treatment is TREAT CANCER LIKE AN INFECTION. Never lose sight of this. The infection may be from fungi, bacteria, parasites, or viruses.
This article discusses a wide varierty of supplements but recommends the 4 basics first and as-necessary addendums after those are addressed. Just recommending the basics keeps it simple and hopefully drives home the point that these basics are so important.
1. Eclectic Institute Intestinal Support is one of the best single systemic antiseptics, despite its name. It used to be called Black Walnut Wormwood and may be effective against viruses, bacteria, fungi, and parasites all over the body. Use it at triple recommended dosage the first week 
(after building up slowly), double recommended dosage the second week, and for a week
every month at recommended dosage afterward. If the problem is
severe it can be used three weeks on and one week
off. Other antiseptics, like Blue Moon or Kroeger Clove capsules and oregano oil (see below),
should be added if more action is needed. The Eclectic
Institute formula is good since it contains two kinds of
wormwood, absynthium and annua, and may also help control mycoplasmas, spirochetes, and
other microbes. Better than the Eclectic Formula may be to use the black walnut hull extract, clove capsules, and wormwood capsules all separately, as Hulda Clark recommends, but this is a hassle compared to using the single product and Clark's regimen does not include wormwood annua (sweet annie) which greatly improves the systemic effects of the supplement. This can be added to Clark's program by adding an additional artemisinin supplement if the Eclectic product is not used.
2. Use Vitamin D. Get 5000IU capsules and use three per day for one week and one per day afterward. Get tested for vitamin D levels after one month to be safest. Note that new research suggests that vitamin K levels should be adequate when using large amounts of vitamin D, so ensure consumption of green leafy vegetables and other sources high in vitamin K or consider a vitamin K supplement.
3. Use non-acidic anti-inflammatory enzymes such as Now Bromelain capsules or Enzymatic Therapy Mega-Zyme, in large amounts. This would be at least 5 capsules between each meal or more as necessary. If I had a brain tumor or other type of cancer where any inflammation was extremely dangerous, I would use double or more this amount. Non-acidic enzymes are important since if they have acidic components like HCL or ox bile, they cannot be taken in large amounts.
Inflammation makes it more likely for cancer to initiate and spread. Enzymes also boost immune system function without making it overactive, provide nutrients to help clean up tumor debris, assist digestion of proteins and oils in the diet, which further boosts the immune system and improves nutritional status, and fight pain and inflammation. If controlling inflammation is of the utmost importance, as in fighting brain cancers, enzymes are the most important supplement.
The most enzyme action for the money is had in pancreatin
supplements. Examples of these include Enzymatic Therapy Megazymes, Twinlab Pancreatin, Wobenzym, and
Healthgenesis Megazyme Forte. One must use a product withoutacidic
components like oxbile and HCL since these cannot be taken
in large enough amounts without causing stomach upset.
Healthgenesis.com Megazyme Forte contains the most
chymotrypsin, which is one of the components of pancreatin
thought to be best in fighting cancer when used in
conjunction with vitamin B-17 (laetrile), but all of these
provide similar action digesting protein and fighting
inflammation. Another company makes a product called
Megazyme Forte which is not the same thing as the one sold
by healthgenesis.com. Note also that
healthgenesis.com's Megazyme 
Forte, unlike Twinlab
Pancreatin or Enzymatic Therapy Megazymes, contains zinc
which if taken in large doses can cause stomach upset.
For doses, use 4 capsules with and between each meal.
Enzymatic Therapy Megazymes are over twice as potent as
the other two so less are necessary - 2 tablets with and
between each meal. Taking with meals assists digestion
and protein assimilation best, taking between meals fights
cancer and inflammation best. If there is pain or no progress in reducing a tumor,
increase the amounts of enzymes. There
is no toxic amount of pancreatin but, again, the Megazyme
Forte can cause stomach upset if used in too high a dose due
to the zinc. Another good pancreatin product is Source Naturals Pancreatin 8X, which has the most activity for the money per serving. See Enzyme Therapy for a more complete discussion of enzymes.
If pancreatin will not or cannot be used for any reason, bromelain (pineapple enzyme) is acceptable. Use only bromelain capsules since bromelain tablets are often sprayed with isopropyl alcohol, a possible cancer catalyst, before packaging.
Enzymes are used long term, but decrease to recommended serving sizes after the problem is solved.
4. Get good quality whey protein and use it in a shake or food for one or two meals or snacks per day. Look for whey without artificial sweeteners or fructose. A good brand is Designer Whey since most of their products are now sweetened with stevia and inulin instead of fructore and sucralose (but still read the ingredients before purchase since some of the old canisters with fructose and sucralose might still be out there). Whey boost glutathione levels in the body better than any other supplement. Using large amounts of vitamin C boosts glutathione levels far more than using a glutathione supplement directly, but whey protein boosts levels far more than vitamin C as well as provides amino acids, sulfur, and protein.
For those who cannot tolerate whey, Natureade makes a soy-free vegetable protein powder. Although soy may provide a few useful nutrients to fight some cases of cancer, long term use may not be beneficial, especially considering soy is a potent protease, including chymotrypsin, enzyme inhibitor. For more information, see Problems with Soy. Plus, no protein supplements except whey boost glutathione levels, including the Soy-Free Natureade product but are only good to provide additional protein in the diet and help keep blood sugar levels lower.
Those are the four basic supplements for fighting cancer and inflammation and boosting the immune system. Below are other supplements often recommended for cancer but probably should not be considered until the basics above are covered.
5. CoQ10. Use in whatever dose one can afford. 200 mg per day is good, 400mg is better, 600mg or more is best. However, taking as little as 30mg per day is still beneficial. Always take CoQ10 with an oily food like a meal, or a few raw walnuts, or an EFA supplement (see below), to greatly increase absorption. CoQ10 is used long term. CoQ10 is often available in softgel form mixed in oil. This is not necessary if sufficient oils are always consumed with the CoQ10, but if they are not, using the softgel is preferred.
6. Oregano oil. My favorite oregano oil supplement is Now Oregano OIl caps. These are gelcaps with some fennel seed and ginger oil mixed in which alleviates burps. The most popular oregano oil supplement is probably North American Herb and Spice Oregano Oil. It is very high quality but using the liquid burns the mouth, so I prefer capsules which allow a good bit to be taken at once (like 2 gelcaps at a time). However, long term use of gelcaps can start to cause cramping in which case, oddly enough, the liquid can usually be used instead. Oregano oil is one of the best if not the best single ingredient supplement to control the widest amount of pathogens. It is highly recommended to use along with the Eclectic Black Walnut Wormwood Para-Fight (formally known as Intestinal Support) if results are not fast enough.
7. Essential fatty acids. (EFAs) Use a molecularly distilled EPA fish oil or other good omega 3 product. Molecular distillation removes toxic metals like mercury which are often found in fish oils. Most quality fish oil products are now of this type. Fish oils come in two types - cod liver oil and "plain" fish oil. Cod liver oil provides less EPA/DHA fatty acids but includes vitamins A and D, which are often helpful in fighting cancer. Plain fish oils provide more EPA/DHA and little if any vitamins A and D. Fish oil can be taken in amounts over the recommended dosage, but using large amounts of cod liver oil long term is not recommended due to the large amount of vitamin A is contains.
Raw nuts can also be used to provide some omega 3
oils. Raw walnuts are good as are raw hulled pumpkin
seeds. If they agree with digestion, one can eat 2 brazil nuts per day, the richest natural source of 
selenium. A
few nuts are especially good to eat with supplements that
are better absorbed with oils, in particular CoQ10, and are
also useful to eat after taking capsule or tablet
supplements to "wash them down" and ensure they do
not get stuck in the throat.
The Budwig diet recommends consuming cottage cheese with flax oil (a tablespoon per half cup to cup of cottage cheese two or three times per day). Flax is an omega 3 oil but it is not in a form that can be used by the body directly - it must first be converted to EPA/DHA. See Essential Fatty Acid Metabolism for more information. This conversion only takes place if there is sufficient protein in the diet and not too many carbs, otherwise using flax oil can actually slow the conversion of all essential fatty acids into body-usable forms, creating a deficiency. Eating adequate cottage cheese provides enough protein where this is not a problem. If this diet is followed, use only organic cottage cheese and a good quality flax oil sold refrigerated in a dark bottle, as from Health From The Sun, Omega Nutrition, or Barlean's. High lignan content is best. One benefit of using omega 3 oils in this manner is that, when omega 3 conversion is effective as it should be, it is the equivalent of using a huge number of EPA fish oil capsules.
Essential fatty acid supplements are used long term as part of a General Maintenance regimen.
8. Vitamin C and Minerals For the most action in severe cases, use vitamin C up to bowel tolerance, but as little as 1g (1000mg) per day is helpful. If dietary mineral status is low due to poor nutrition, vitamin C must be used with adequate minerals. Since vitamin C causes increased elimination, sufficient mineral intake must be assured or it could cause a deficiency. For minerals, use a 1:1 ratio calcium magnesium like Solaray Cal-Mag Citrate. This is a cleansing form since it contains so much magnesium. Or, use a 1:1 cal-mag ascorbate product like Nutribiotic Hypo-Aller C to provide both minerals and vitamin C.
Vitamin C and minerals are used long term. After the problem is solved, continue to get adequate calcium (50% RDA or more) and magnesium (100% RDA or more) daily and use vitamin C in low to medium dose.
9. A liver cleansing supplement. There is much liver, kidney,
and other organ cleansing action with the recommendations above, but it may be
necessary to clean petrochemicals out of the liver quickly. If the liver's
function is severely compromised, this becomes the most important supplement. Good combination products for this purpose are FutureBiotics
Silymarin Plus or 
Now
Silymarin. Futurebiotics is best for immediate and strong cleansing action taken at the full recommended dosage for two to three weeks or longer as needed, then one weekend per month. Now Silymarin is good for maintenance since the base it contains provides antioxidant and antiseptic properties and can be taken one capsule before bed long term.
10. Basic multivitamin regimen Do not use B vitamins including a multivitamin without first taking antiseptic supplements since they can otherwise stimulate fungi and parasites. A multivitamin can be taken long term if desired if it provides noticeable benefits in energy levels and well being.
If additional measures were required, I would consider cleansers and antiseptics like the Hoxsey formula. Gaia makes a good one called Hoxsey Red Clover Formula (now known as Red Clover Supreme). They made another deep tissue cleanser called Scudder's Alterative that may work better for some people although it has been discontinued. Use at recommended dose.
Juicing provides nutritional and immune boosting benefits
but be sure that they do not raise blood sugar levels.
One way to accomplish this is to add protein (like whey) and
olive or flax oil 
to juices which have a high glycemic
index (like carrot or fruit juices.) The Vita-Mix
blender is, IMO, the best juicer since there is no waste and
cleanup is easiest.
Glyconutrients and polysaccharides may be helpful against some diseases including cancer, but the products sold through multi level marketing schemes are very expensive (probably 3 times more than they should be, if other overhyped MLM products are any indication). Glyconutrients are also available from aloe juice, plus aloe juice has many other beneficial ingredients that are not found in typical glyconutrient products. George's aloe juice is the most highly recommended type. It is fractionally distilled to remove the laxative components, tastes almost like water, can be used in whatever amount is necessary, and is reasonable in cost (around $20 per gallon). Of course, like any aloe juice, George's is also excellent used topically.
One mistake people make when formulating a cancer regimen
for themselves is they forget the basics. Taking
advice from different people, often herb store clerks, they
end up with 40 or 50 different supplements with no idea
which are the most beneficial for their condition when they
realize they cannot possibly take them all. The basics
are to be continuously using antineoplastic and antiseptic
supplements or performing other measures to control
infection be it from virus, bacteria, fungi, or parasites,
controlling exposure to toxic elements, and 
ensuring
consumption of nutrients often missing from the diet like
sufficient vitamin C, enzymes, EFAs, and minerals.
It helps the immune system far more to control an infection directly, avoid toxins which impair its function, and ensure the basic nutrients needed for its function rather than take high priced immune stimulants. For example, I have seen people taking IP-6 and making progress only to be talked into instead using an expensive mushroom supplement by an herb store clerk (saying, "it contains IP-6, too!" - yeah, about 50 times less) and start losing progress despite spending hundreds per month on this one supplement. I have seen people write or recite a long list of supplements they were taking for cancer, many very expensive, and there not be a single one with strong antiseptic action. Don't make this mistake.
The following was written by Dr. Richard Loyd and posted to the rife lists . The 90% Percent Solution |
Prostate Cancer Update Life Extension Update Exclusive Vitamin E succinate inhibits prostate tumor growth in laboratory studies A report published in the May 15, 2006 issue of the International Journal of Cancer revealed the findings of researchers at H. Lee Moffitt Cancer Center in Tampa, Florida and their colleagues at Southern Illinois University School of Medicine that a form of vitamin E (VE) known as vitamin E succinate (VES) suppressed prostate cancer cell growth in culture as well as in a mouse model of the disease. Mokenge P. Malafa and his team used a rat prostate cancer cell line, and two androgen receptor-negative and one androgen receptor-positive human prostate cancer cell lines for the current study. The cells were incubated with various concentrations of vitamin E succinate, vitamin E (nonsuccinate), succinic acid, ethanol, or no additions, and cell activity was studied. Vitamin E succinate significantly inhibited growth of the rat prostate cancer cells at 48 hours at a concentration for which vitamin E or succinic acid alone were ineffective. It was discovered that apoptosis, or programmed cell death, was the mechanism behind the growth inhibition. Vitamin E succinate also helped inhibit the growth of the human prostate cancer cells by the same mechanism. In another experiment using mice who received prostate cancer tumor grafts, daily injections of 50 or 100 milligrams per kilogram vitamin E succinate were associated with tumor growth suppression compared to untreated mice. Although the 50 mg/kg dose appeared to be ineffective at preventing metastasis, mice who received the higher dose of vitamin E succinate had dramatically fewer metastatic nodules in the lungs than untreated mice. “We have demonstrated for the first time that VES, a derivative of VE, is capable of inhibiting prostate cancer growth in vivo,” the authors announced. “Further studies of the antitumor effects of VES in vivo will aid in the design of clinical trials to incorporate the use of this micronutrient in the treatment of human prostate cancer,” they conclude. Protocol from Life Extension Foundation Prostate cancer: metastasized/late stage Not all prostate cancer (PC) is systemic, anymore than all breast cancer or other tumor types are systemic. If they were, we would never cure any man or woman of PC, breast cancer, or any other malignancy. Physicians claiming that every man with PC needs androgen deprivation therapy (ADT) as primary and sole therapy are blindly ignoring the growing numbers of men who present 8 to 15 years after radical prostatectomy (RP) or radiation therapy (RT) with a flat PSA graph. Emphasis on the use of routine prostate specific antigen (PSA) monitoring starting annually at the age of 40 with PSA velocity and doubling time determinations as a standard part of PSA reporting will increase the numbers of men diagnosed earlier, with a lower tumor burden, and cured with local modalities of treatment (Labrie et al., J. Clin. Endocrinol. Metab., 1995; Labrie et al., Urology, 1996). PSA testing with these enhancements should start earlier, at age 35, in men with a familial history of PC. The difference in treating early PC versus more advanced PC relates to the issue of cure as opposed to control. Early PC has the potential for cure via a local therapy combined with the use of ADT in situations where the tumor volume compromises the curative ability of local therapy such as RT (including seed implantation) or cryosurgery. When PC spreads to the capsular interface and leaves the prostate gland, it reflects a change in the biologic nature of the cancer. The PC now is expressing its more aggressive nature in its ability to spread and metastasize. Why? The aggressiveness of these tumors appears to directly correlate with the proportion of higher Gleason grade cells. This frequently involves multiple clones of PC cells-some androgen-sensitive, but others androgen-insensitive, and/or possibly androgen-altered (Aihara et al., Urology, 1994; Brawn, Cancer, 1983). This heterogeneity appears related to tumor size or burden. As the tumor burden increases by cell division, the chances of gene mutation increase, which in turn may lead to androgen or drug-resistant tumors. Such mutations likely result from the activation of oncogenes or the inhibition of tumor suppressor genes. http://www.lef.org/protocols/prtcl-094.shtml Featured Products
Prostate cancer cells are wusses when it comes to hot chilies Prostate cancer cells would rather commit suicide than feel the burn of hot chili peppers (or, at least, one ofchili peppers' components), according to a report published in the March 15, 2006 issue of Cancer Research. Scientists at the Samuel Oschin Comprehensive Cancer Institute at Cedars-Sinai Medical Center along with colleagues from the University of California at Los Angeles found that giving capsaicin, the compound in jalapeño chilies responsible for a burning sensation when consumed, to mice in whom human prostate cancer tumors were implanted caused approximately 80 percent of the cancerous cells to undergo apoptosis (programmed self-destruction). The dose given to the mice was the equivalent of giving a 200 pound man 400 milligrams capsaicin three times per week, which is the amount provided by three to eight fresh habañera peppers. In separate studies using androgen-dependent and independent cell cultures, capsaicin reduced cell proliferation and lowered the production of prostate specific antigen (PSA), a protein produced by prostate tumors. http://www.lef.org/whatshot/index.html#pcca ------------------------------ From Mike at truerife.com "The following information is for research purposes only, and does not claim to present a cure for any disease or health condition." Understanding the function of cancer on its most basic level can often result in getting a better grasp on other avenuesof targeting or even preventing malignancy. This is deep stuff, but it is worth the time for serious researchers to evaluate. The Body's Control of Angiogenesis Angiogenesis occurs in the healthy body for healing wounds and for restoring blood flow to tissues after injury or insult. In females, angiogenesis also occurs during the monthly reproductive cycle (to rebuild the uterus lining, to mature the egg during ovulation) and during pregnancy (to build the placenta, the circulation between mother and fetus). The healthy body controls angiogenesis through a series of "on" and "off" switches:
Angiogenesis may switch off in as little as two to fourteen days.
When angiogenic growth factors are produced in excess of angiogenesis inhibitors, the balance is tipped in favor of blood vessel growth. When inhibitors are present in excess of stimulators, angiogenesis is stopped. The normal, healthy body maintains a perfect balance of angiogenesis modulators. In general, angiogenesis is "turned off" by the production of more inhibitors than stimulators. History of angiogenesis research 1787 - British surgeon Dr. John Hunter first uses the term 'angiogenesis' (new blood vessel growth) to describe blood vessels growing in the reindeer antler. 1935 - Boston pathologist Dr. Arthur Tremain Hertig describes angiogenesis in the placenta of pregnant monkeys. 1960's - Judah Folkman first hypothesized in the 1960's that angiogenesis is also integral to the complex biology that enables and encourages the growth of tumors and other forms of cancer. Folkman has spent the last four decades validating this hypothesis, beginning with a publication in the New England Journal of Medicine in 1971. In this paper, he proposed the revolutionary concept that tumors are unable to grow beyond a certain size unless they have a dedicated blood supply, and that successful tumors secrete an unknown substance (which he then called tumor angiogenesis factor, or TAF) that encourages new blood vessel growth. The process of angiogenesis, Folkman argued, helps transform a tumor from a small cluster of mutated cells to a large, malignant growth. According to the National Cancer Institute, solid tumors cannot grow beyond the size of a pinhead, that is, 1-2 cubic mm, without inducing the formation of new blood vessels to supply the nutritional needs of the tumor. So without the tumors promotion of angiogenesis, tumor growth would terminate at a point where it would not be life threatening. In 99% of cases observed by researchers, this is exactly what happens.The fact is that many people go to their grave with these small cancerous tumors never affecting the quality of their lives,but in 1% of cases, the tumor is able to generate its own TAF or aniogenesis factor allowing for uncontrolled cancerous tumor growth, in effect the switch is now locked to the ON position for blood vessel growth. Uncontrolled cancer malignancy has now begun. Since rapid vascularization and tumor growth appear to occur concurrently, interrupting the vascular growth cycle is paramount to overcoming or even preventing malignancy. Or to put is simply, if one could turn the angiogensis switch to OFF, tumor growthwould stop, and may even regress, or would have never started at all. ENTER ribonucleotide reductase (The following information is contains information from: http://www.dukemednews.duke.edu/) A gene labeled RRM1 is responsible for the production of ribonucleotide reductase. Ribonucleotide reductase or RR, has been known for 30 years or so and has been studied biochemically, andis required for cell viability and cell repair. It is also a necessary component for angiogenesis. If you can knock out RRM1, there is no way a cell can overcome the lack of ribonucleotide reductase and survive." Potentialtherapy could, therefore, either block the enzyme, rendering it ineffective, or could target the remaining copy of the RRM1 gene to prevent it from producing the enzyme. As with all cancer treatments, however, there needs to be selectivity so that cancer cells are killed but normal cells are left alone as much as possible. Normal cells have two copies of RRM1 and would be more resistant than a cancer cell that has 1 copy of the RRM1 gene. With no ribonucleotide reductase active, the cancer will die, tumors willstop growing, angiogeneses willbe turned OFF. While normal cells may be affected also, they should have enough residual enzyme activity to survive and wouldn't become cancerous just because of diminished RRM1 activity.The gene doesn't make cancer, it just makes cancer spread when angiogenesis is out of balance." Two copies of the RRM1 geneare good; no copies and the cell dies. One copy seems to make the cell prone to metastasizing or angiogenesis in the case of tumor growth. Currently, new drugs are being developed known as andiogenesis inhibitors. Enter Electrotherapy: Since the introduction of theEffectrolysis Hydrotherapy system, we have received positive reports as well as blood work for a variety of cancers. What has been puzzling is that many of these reports came from individuals who were running simple detox frequencies only. Since these frequencies have no known association with Rife Cancer frequency research, whatmay bethe mechanism for these positive reports? A clue as to what may be happening may have to do with the enzyme RR (ribonucleotide reductase) which some researchers believe to be at the core of cancerous growth. Asimple wayof blocking this enzyme is suggested by the fact that at the center of this enzyme is a lone electron (free-radical) which is essential for its activity. It has been demonstrate that such free radicals can be disabled with a small amount of electrical current being passed through the tissue. Evidence is mounting that the vortex of cancerous growth and angiogenesisis centered around the enzyme ribonucleotide reductase. In the 1985 study, electrotherapy was shown to consistently and progressively reduce tumor mass. This consisted of five one-hoursessions over 5 days at 2.4 milli-ampere! Researchers who are pursuing these protocols state “this cancer treatment should be effective in treating various solid cancers such as bladder, bone, brain, breast, cervical, colon, esophagus, kidney, liver, lung, ovarian, pancreatic, prostate, rectal, skin, stomach, testicular, throat & uterine cancers.” Rather this is the mechanism of the Effectrolysis hydrotherapy systems or other conventional Rife systems positive reports is not known, and certainly much more research needs to be done.However, it may provide interesting insight and clues on what may be happening during the sessions, and may provide a new avenue of research for resonant initiated field effects. SUPPLEMENT GREEN TEA : "Green tea has also been shown to help prevent metastasis. Cancer cells secrete special enzymes called collagenases in order to penetrate and colonize various tissues. It is the metastatic (angiogenesis)process that is lethal, not the primary tumor. Hence finding substances that can prevent metastasis is of prime importance in fighting cancer. A study done at the University of Shizuoka in Japan found that epigallocatechin gallate does in fact inhibit the secretion of collagenases by tumor cells (in this study, highly metastatic lung cancer cells), thus arresting their ability to invade normal tissue. Black tea theaflavins were also effective. There is also additional evidence that green tea polyphenols help inhibit angiogenesis, or the growth of new blood vessels that nourish the tumor." Mike -------- Life Extension Update Exclusive Vitamin C works against cancer (but maybe not the way you thought) Researchers from Johns Hopkins report in the September, 2007 issue of the journal Cancer Cell that vitamin C can indeed help prevent cancer as has been claimed for years by a number of scientists including Linus Pauling, but it appears to do so in a different manner than that which earlier researchers proposed. While it had been believed that the well known antioxidant property of vitamin C prevented cancer by protecting DNA from free radical damage, the latest research unveils a new mechanism: that of preventing the ability of a tumor to grow in a reduced oxygen environment. Johns Hopkins professor of medicine and oncology Chi Dang, MD, PhD and his associates tested the ability of vitamin C as well as N-acetyl-cysteine, another antioxidant, in mice implanted with human lymphoma or liver cancer cells, both of which produce a high number of free radicals. Control groups of mice implanted with the cancers received no antioxidant supplementation. When the researchers examined DNA from the mice that did not receive antioxidant treatment, a lack of significant damage was observed. "Clearly, if DNA damage was not in play as a cause of the cancer, then whatever the antioxidants were doing to help was also not related to DNA damage," lead author Ping Gao, PhD, said of the finding. The team found that a protein known as hypoxia-induced factor (HIF-1), which is dependent upon free radicals, was diminished in antioxidant-treated animals. The protein enables tumors to survive in the low oxygen environment of rapidly growing tumors. "When a cell lacks oxygen, HIF-1 helps it compensate," Dr Dang explained. "HIF-1 helps an oxygen-starved cell convert sugar to energy without using oxygen and also initiates the construction of new blood vessels to bring in a fresh oxygen supply." The finding was verified by the engineering of cancer cells to contain a variant of HIF-1 that was not dependent upon free radicals. Antioxidants proved to be powerless against these cancerous cells. "The potential anticancer benefits of antioxidants have been the driving force for many clinical and preclinical studies," Dr Dang noted. "By uncovering the mechanism behind antioxidants, we are now better suited to maximize their therapeutic use." "Once again, this work demonstrates the irreplaceable value of letting researchers follow their scientific noses wherever it leads them," he added. Complementary complementary cancer therapies Vitamin A derivatives, known as retinoids, protect against the development of various cancers, including those of the skin, breast, and lung (Clarke N et al 2004; Khera P et al 2005). Dietary supplementation with synthetic vitamin A for 12 months in liver cancer survivors prevented recurrence of this cancer (Takai K et al 2005). In addition to preventing cancer, vitamin A derivatives have been used to cure acute promyelocytic leukemia (Clarke N et al 2004). Vitamin C. Long-term human studies have shown that vitamin C dietary supplements, when used in conjunction with other antioxidants, can reduce the risk of developing cancer (Hercberg S et al 2004). Similar results were found for cancers of the prostate (Meyer F et al 2005) and lung (Mooney LA et al 2005; Wright ME et al 2004). Clinical studies have shown that vitamin E can reduce the risk of prostate and lung cancers, particularly when used in combination with selenium supplements (Helzlsouer KJ et al 2000; Woodson K et al 1999). Regular and long-term (over 10 years) use of vitamin E reduces the risk of death from bladder cancer (Jacobs EJ et al 2002). Similarly, the use of vitamin E supplements for longer than three years slightly reduces the risk of recurrence among breast cancer survivors (Fleischauer AT et al 2003). --------------------------- |
Rife Frequencies, Annotations, and Comments CAFL - Some of the general sets for Cancer Cancer (Basic comprehensive set. A complete set like this, or rotation of the general cancer sets, or Rife Technology's intensive carcinoma and sarcoma banks are used as Basic sets. Sets listed below for specific types are to be used in addition to basic sets. Also add frequencies determined to be beneficial from scans. Increase run times on frequencies thought to be most effective as detox allows. Don Tunney now includes E_coli_1 frequencies with Resonant Light’s intensive regimens. Also use 11,780,000Hz if device is capable. James Bare states that 10025 may be master frequency for cancer in general, 10026 for sarcoma. Use + and - 3Hz sweep about 10025, building up to longer periods like 5 min per freq) - 10000, 11780, 21275, 17034, 11430, 10025, 6766, 6064, 5000, 3713, 3176, 3040, 2950, 2876, 2790, 2720, 2452, 2189, 2182, 2128, 2127, 2084, 2048, 2008, 1604, 1552, 1489, 880, 854, 800, 784, 776, 766, 728, 690, 683, 676, 666, 524, 464, 333, 120, 20 Cancer_general_1 - 10000, 5000, 3176, 2720, 2489, 2189, 2184, 2128, 2084, 2050, 2008, 880, 854, 800, 784, 728, 666, 524, 464, 333, 304, 120 Cancer_general_2 - 10000, 3176, 3040, 2720, 2489, 2182, 2127, 2048, 2008, 1862, 1552, 880, 802, 786, 727, 665, 664, 465, 304, 125, 96, 72, 64, 20 Cancer_general_3 - 10000, 3176, 2950, 2180, 2128, 2049, 2008, 1865, 1488, 943, 886, 866, 776, 732, 728, 690, 676, 650, 523, 442, 414, 304, 240, 128 Cancer_BX_virus (carcinoma virus. Sweep up and down 1000hz on MHz freqs and use 0.01Hz sweep on 2876 and 2790) - 11780000, 17033662, 1604368, 21725, 17034, 46015.6, 23007.8, 11503.9, 10025, 3713, 2876, 2790, 2128, 2008, 1604 Cancer_BX2_TR (also use 21275, 20080, 17220, 1604000, 11780000 if device capable) - 5318.8, 8610, 8020, 5278.3, 1675, 5020, 2128, 2127.5, 2127, 2663, 334, 2655, 5388.5, 2385, 6687.3, 3324, 8836.9, 2521, 7356, 2787.5, 5575, 8368.2, 1566.4, 2008, 5013, 5013.5, 10025, 10026, 10027, 7037.5, 263.11 TrueRife - Selected frequency sets in F100 format with comments Cancer_BX #1 hour #The Rife frequency instrument kills the "normal" carcinoma cancer cell by rupturing the thousands of BX cancer viruses they contain and thereby dumping the BX cancer virus contents into the cancer cell cytoplasm. This BX cancer virus as Rife named it in 1931 is not a virus by the normal standard usage of the term today. Rife based his definition on the fact that the BX cancer virus could pass through the finest Berkefeld porcelain filter of the time (000 filter). The BX cancer virus is ovoid in shape, .066 microns along the major axis and .05 microns along the minor axis. It is motile, driven by a proton transport flagella the same as its bacterial parent, the E-coli bacteria. When the BX cancer virus is ruptured it spills out its genome, ribosomes, RNA, enzymes, and various proteins. When thousands of these ruptures occur all at once in a carcinoma cancer cell the results are fatal to the cancer cell. A similar situation occurs in the sarcoma cancer cell when the BY cancer viruses are all disintegrated at once. The BY cancer virus is another form of the BX cancer virus which Rife found caused sarcoma cancer after it had been exposed to prolonged ultraviolet light exposure. #The first step in dealing with cancer electronically must be to eliminate all Bacillus Lichenformis from the body as it appears to be both a tumor promoter and a mutagen. Tumors will tend to grow or recur with this organism present. Also, any significant infection with this organism depresses the immune system and severely drains energy from the body, possibly one of the main reasons that newly diagnosed cancer patients often deteriorate so rapidly. Most people with a depressed immune system are infected with nanobacteria and that must be eliminated also. SEE: Bacillus lichenformis Program dwell 900 Posted by : James Bare Although we in the R.I. F. E. community have been using a few frequencies that affect cancer, modern day researchers have discovered at least 19 ( if not more) that also affect cancer. Some of these in a very profound manner. Some researchers have found that different cancers need very different frequencies to produce effectiveness. The frequencies can vary, not by a few Hz, but by 10's of KHz! |
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