• Phase 1 of Cancer: Inescapable Shock
  • Phase 2 of Cancer: Adrenaline Depletion
  • Phase 3 of Cancer: The Cancer Fungus
  • Phase 4 of Cancer: Niacin Deficiency
  • Phase 5 of Cancer: Vitamin C Depletion
  • Phase 6 of Cancer: Immune Suppession
  • Cancer-Grief Link
  • Cancer-Anger Link
  • Cancer-Fungus Link
  • Beating Cancer with Nutrition
  • Dr Ryke Geerd Hamer
  • EFT and Cancer
  • EMF Radiation and Cancer
  • Essiac Tea and Cancer
  • Fever Therapy and Cancer
  • Garlic and Cancer
  • Gerson Therapy Cancer Diet
  • God Cancer Cure
  • High Dose Vitamin C Cancer Treatment
  • Whole Body Hyperthermia Cancer Treatment
  • Johanna Budwig Cancer Diet
  • Cancer and Detoxing the Liver
  • Melatonin, Meditation and Cancer
  • Niacin Vitamin B3 and Cancer
  • Oxygen Ozone Cancer Therapy
  • Photodynamic Therapy for Cancer
  • Prayer, God and Cancer
  • Acid-Alkaline pH and Cancer
  • Who Survives Cancer?
  • Baking Soda (Sodium Bicarbonate) and Cancer
  • Massage, Cortisol and Cancer
  • The Brandt Grape Cure and Cancer
  • Cesium Chloride Cancer / DMSO
  • MMS Cancer
  • MMS Cancer Study
  • MMS Cancer Testimonials
  • Overnight Cure for Cancer
  • Avemar Cancer Treatment
  • Hulda Clark Parasite Cancer Cleanse: Clarkia
  • DMG Cancer Immune System
  • Vipassana Meditation and Cancer
  • Guided Relaxation for Cancer
  • Lavender Oil Therapy for Cancer
  • The Cancer Healing Guide
  PSYCHO-ONCOLOGY: DISCOVER HOW STRESS CAUSES CANCER

Psycho-Oncology: Discover How Stress Causes Cancer


Phase 1 of Cancer: Inescapable Shock
Phase 2 of Cancer: Adrenaline Depletion
Phase 3 of Cancer: The Cancer Fungus
​Phase 4 of Cancer: Niacin Deficiency
Phase 5 of Cancer: Vitamin C Depletion
Phase 6 of Cancer: Immune Suppression


HIGH DOSE VITAMIN C CANCER TREATMENT

High dose vitamin C can be take orally or intravenously in the treatment of cancer to stop cancer cell growth. Vitamin C also enhances the immune system by increased lymphocyte production, walls off tumours by stimulating collagen formation, prevents metastasis, expedites wound healing after cancer surgery, neutralizes carcinogenic substances and prevents cellular free radical damage. High dose oral or intravenous vitamin C therapy also has an ameliorating effect on the side effects of the highly oxidative chemotherapeutic agents. Some of the side effects of chemotherapy are so severe that many patients stop therapy as a result. It has been shown to increase the lifespan of some cancer patients when receiving 10-100 grams 2-7 times per week, notably when chemotherapy has not already been used. High dose vitamin C iv or oral treatment inhibits hyaluronidase, an enzyme tumours use to metastasize and invade other organs throughout the body. It induces apoptosis to help program cancer cells into dying early and it corrects the almost universal scurvy in cancer patients. Cancer patients are normally tired, listless, bruise easily, and have a poor appetite. They don't sleep well and have a low threshold for pain. This adds up to a very classic picture of scurvy that generally goes unrecognized by their conventional physicians. When cancer patients receive high doses of oral or intravenous vitamin C they report pain level goes down and are better able to tolerate chemotherapy. They bounce back quicker since the high doses of vitamin C reduces the toxicity of the chemotherapy and radiation without compromising their cancer cell killing effects. High dose oral or intravenous vitamin c cancer treatment can help patients withstand the effects of their traditional therapies, heal faster, be more resilient to infection, develop a better appetite, and remain more active overall. These things promote a better response to overall cancer therapy.

IMPORTANT NOTE: If you decide to stop taking large doses of vitamin C, it is important to wean off the dose slowly. This is because the body will continue to use high doses of vitamin C at the level it is used to, and this can leave the already weakened cancer patient in an even further weakened state, by depleting the body of important vitamin C reserves. [Note: The Holy Spirit of God speaks of this in-depth under the role of lemons as a life extender]

VITAMIN C IN THE TREATMENT OF CANCER: A SUMMARY

Vitamin C in the Treatment of Cancer, by Kathleen A Head, ND. "The Vale of Leven Studies: Most of the studies on vitamin C and cancer relate to its protective effect, rather than use of the vitamin for the treatment of active cancer. The Vale of Leven studies conducted by Ewan Cameron, MD and his associates, (later including Linus Pauling, PhD), at his hospital in Loch Lomondside, Scotland, are among the few exceptions. In preliminary studies which began in November 1971, a small group of patients with advanced cancer were given 10 grams of sodium ascorbate daily. The initial testing was an uncontrolled study, conducted on 50 patients. Seventeen of these patients exhibited seemingly no response, 10 a minimal response, 11 retardation of the tumour growth, 3 ceasing of the tumour growth, 5 regression of tumour growth with long-term survival, and 6 experienced haemorrhage and necrosis of the tumours, which destroyed the tumours but killed the patients in the process. An evaluation of the life expectancy of these first 50 "terminally ill" patients treated with ascorbate yielded promising results. 

Based on data from previous similar groups of patients, it was expected that 90 percent of the group would be dead within three months of being labelled "terminal." When 10 g ascorbate was prescribed daily (beginning at the time the patient was labelled "terminal"), by the 100th day of treatment the mortality rate was only 50 percent. Of the remaining 25 patients, 20 died between days 110 and 659, with an average survival time of 261 days; and five had an average survival time of greater than 610 days. Subsequently, a controlled retrospective study was conducted, comparing survival times of 100 terminally ill cancer patients at Vale of Leven Hospital with 1,000 matched controls from the same hospital. The patients were randomly selected from the database of those terminal cancer patients who had received ascorbate. Each ascorbate-treated patient was matched with 10 controls from the same hospital of the same age, sex, and type and stage of cancer who had not been prescribed vitamin C. In 90 percent of the cases, the ascorbate-treated group lived three times longer than the control group. For the other 10 percent, long-term survival made it impossible to assess survival time with certainty, but at the time of publication of the study, the ascorbate group exhibited greater than 20 times the survival rate of the control group. Having been criticized by some investigators for not assuring the subjects were randomly chosen from the same representative subpopulations in the treated and control groups, a second retrospective evaluation at the Vale of Leven hospital was undertaken in 1978 again with 100 patients receiving ascorbic acid compared to 1,000 matched controls without vitamin C. Most of the ascorbate-treated group and about half the controls were the same subjects as in the initial study. This time, since there are different mean survival times for different types of cancer, the groups were further divided according to types of cancer, and controls carefully matched. In addition, the groups passed several "randomness" tests. In each of the nine types of cancer the ascorbate group had a considerably longer survival time than their matched controls. At the time of evaluation, eight patients in the vitamin C group were still living, while no one was alive in the control group; this resulted in 321+ days longer lifespan for the vitamin C treated group. Factoring out those in the ascorbate group who were still living at the time of evaluation, the vitamin C group lived an average of 251 days longer than the control group. 

Cameron and Pauling later evaluated the first 500 "terminal" cancer patients to receive ascorbate. In most cases, subjective improvement ­ increased feeling of well-being, more energy, more alertness, decrease or elimination of pain, better appetite­ were noted by the ascorbate patients. Cameron reported a quite dramatic relief of bone pain from metastases in four out of five patients. Objective improvements included a decrease in malignant ascites and pleural effusion, relief from hematuria, some reversal of hepatomegaly and jaundice, and decreases in erythrocyte SED rate and serum seromucoid levels, all accepted indicators of a decrease in malignant activity. Furthermore, patients who had been on large doses of narcotics, such as morphine, for pain relief, showed none of the typical withdrawal symptoms. Based on the above cited studies the researchers concluded: "It is our conclusion that this simple and safe treatment, the ingestion of large amounts of vitamin C, is of definite value in the treatment of patients with advanced cancer. Although the evidence is as yet not so strong, we believe that vitamin C has even greater value for the treatment of cancer patients with the disease in earlier stages and also for the prevention of cancer."

The Vale of Leven protocol called for a ten-day course via intravenous (IV), continuous slow-drip infusion of sodium ascorbate in half-strength Ringer's Lactate Solution. After the IV treatment, assuming the patient was able to take medication by mouth, an oral dose of vitamin C was begun at a dose of 2.5 grams every 6 hours for a total of 10 grams in 24 hours. The dosage varied somewhat, ranging from 10-30 grams daily, and was continued indefinitely. The goal was to maintain plasma ascorbate levels of at least 3 mg/dl. The researchers reported generally a subjective improvement in well-being, vigour, pain relief, and appetite was apparent within 5-7 days. Increased energy was believed to be a result of improved carnitine synthesis with a resulting increase in triglyceride transport into cell mitochondria.

Japanese Studies:  Uncontrolled trials conducted at two different hospitals in Japan during the 1970s also confirmed the increase in survival time of terminal cancer patients supplemented with ascorbate. At the Fukuoka Torikai Hospital, the average survival time after being labelled "terminal" was 43 days for 44 patients supplemented with low levels of ascorbate (less than 4 grams daily), and 246 days for 55 patients supplemented with higher dosages of ascorbate (greater than 5 grams daily - averaging 29 grams daily) and starting at the time of "terminal" diagnosis. The researchers found no differences in survival times between the groups receiving 5-9 grams daily and those receiving 10-29 grams daily. A decline in effect was noted in those receiving 30-60 grams daily. They found the best results with uterine cancer, and the smallest increases in survival time with lung and stomach cancer. Effectiveness of ascorbate was also observed at the Kamioka Kozan Hospital where 19 terminally-ill control patients survived an average of 48 days compared to six patients on high levels of vitamin C who lived an average of 115 days, or 2.4 times longer than the control group. These researchers also reported the improved quality of life observed in the Scottish studies.

Mayo Clinic Studies:  In an attempt to either duplicate or refute the Cameron and Pauling results, the Mayo Clinic initiated a test on 150 patients. Subjects were randomly divided into two groups, one group of 60 received 10 grams of ascorbic acid daily in four divided doses while the control group of 63 received an equal number of placebo capsules. After randomization, 27 patients elected not to participate and comprised a third "no treatment" group. Treatment was continued until death or until the patient was no longer able to take medication orally. The two groups were evenly balanced with regard to age, sex, tumour site, initial performance status, and previous treatment. Fifty-eight percent of those receiving placebo and 63 percent of those receiving ascorbate reported subjective improvement in symptoms during the treatment period. The researchers reported no significant difference between the vitamin C and placebo groups in regard to survival time; however, the 27 patients who received no treatment experienced a significantly lower survival time, living an average of 25 days compared to an average of 51 days for the vitamin C or placebo groups. All but nine of the 123 subjects had received prior chemotherapy, radiation, or both."

VITAMIN C NOT AS EFFECTIVE AFTER CHEMOTHERAPY

Vitamin C and cancer: Linus Pauling is considered the pioneer in the use of oral and intravenous vitamin c in the treatment of cancer. His documented studies in extending cancer survival using large doses of Vitamin C are seen as a benchmark by all those who seek to replicate or refute the beneficial claims of Vitamin C. In 1979, the Mayo Clinic undertook a clinical study to replicate or refute the earlier studies of Linus Pauling. The study participants (with a few exceptions) had all received chemotherapy PRIOR to being given ORAL doses of Vitamin C. The study concluded by the Mayo Clinic reported no evidence that large doses of Vitamin C help in extending cancer survival. The following is a letter from Linus Pauling to the Editor of The Times magazine who reported "Vitamin C Fails as a Cancer Cure" as a result of the Mayo Clinic findings. By Linus Pauling (October 24, 1979). "To the Editor: An article in your Sept. 30 Week in Review section, "Vitamin C Fails as a Cancer Cure" (with reference to me in the first sentence), said that a controlled study of 150 Mayo Clinic patients with advanced cancer, published in the New England Journal of Medicine, had shown no evidence that large doses of vitamin C help. This is indeed what was reported by the Mayo Clinic investigators. They themselves and The Times article do not point out, however, that the population of cancer patients investigated in the Mayo Clinic was so different from that investigated by my associate Dr. Ewan Cameron in Vale of Leven Hospital, Loch Lomondside, Scotland, that the results observed in the Mayo Clinic study cannot be considered to refute the results observed in the study in Scotland. The chief investigator in the Mayo Clinic study wrote to me last year that he hoped to repeat Dr. Cameron's work as closely as possible. I then wrote to him, pointing out that cyto-toxic chemotherapy damages the body's protective mechanisms to such an extent that subsequent treatment with Vitamin C would not be expected to have much value, because Vitamin C functions largely by potentiating these protective mechanisms. I recommended strongly that only patients who had not received chemotherapy be used in the Mayo Clinic study. This recommendation, however, was ignored.  Nearly all the patients in the Mayo Clinic trial had received courses of chemotherapy, whereas only 4 percent of those studied by Dr. Cameron had received chemotherapy. The Vale of Leven study showed that large doses of Vitamin C have great value for cancer patients who have NOT received chemotherapy. The Mayo Clinic study answers an important question in that it verifies that treatment with Vitamin C is far less effective for patients whose immune systems have been damaged by courses of chemotherapy." http://profiles.nlm.nih.gov/MM/B/B/R/R/_/mmbbrr.pdf

NATIONAL INSTITUTES OF HEALTH:
​VITAMIN C AND ADVANCED CANCER SURVIVAL CASES

National Institute of Health / National Cancer Institute – “Early clinical [Cameron/Pauling] studies showed that high-dose - oral OR intravenous vitamin c iv, may improve symptoms and prolong life in patients with terminal cancer. Double-blind placebo-controlled [Mayo Clinic] studies of oral vitamin C therapy showed no benefit. Recent evidence shows that oral administration of the maximum tolerated dose of vitamin C (18 g/d) produces peak plasma concentrations of only 220 µmol/L, whereas intravenous administration of the same dose produces plasma concentrations about 25-fold higher. Larger doses (50–100 g) given intravenously may result in plasma concentrations of about 14 000 µmol/L. At concentrations above 1000 µmol/L, vitamin C is toxic to some cancer cells but not to normal cells in vitro. We found 3 well-documented cases of advanced cancers, confirmed by histopathologic review, where patients had unexpectedly long survival times after receiving high-dose intravenous vitamin c iv therapy. We examined clinical details of each case in accordance with National Cancer Institute (NCI) Best Case Series guidelines. Tumour pathology was verified by pathologists at the NCI who were unaware of diagnosis or treatment. In light of recent clinical pharmacokinetic findings and in vitro evidence of anti-tumour mechanisms, these case reports indicate that the role of high-dose intravenous vitamin c iv therapy in cancer treatment should be reassessed.”

Dr. Mark Levine of the National Institutes of Health in Bethesda, Maryland, and colleagues note that, in vitro, vitamin C is toxic to some cancer cells but not normal cells at concentrations above 1000 µmol/L. IV doses in the range of 50-100 g result in plasma levels of about 14,000 µmol/L. The team analyzed clinical and histological data from three patients with advanced cancer who responded to high-dose IV vitamin C. The first patient was a 51 year-old-women with advanced renal cell carcinoma, treated with nephrectomy, and several small lesions in the lung "consistent with metastatic cancer." She received IV vitamin C 65 g twice a week for 10 months, in combination with other alternative therapies, including thymus protein extract. Repeat chest radiography revealed one small spot, assumed to be a scar. Five years later, new lung masses were detected. The patient again received intravenous vitamin c iv, with unsuccessful results. The second patient, a 49-year-old man, had bladder cancer with multiple satellite tumours. He received IV vitamin C 30 g twice a week for three months, followed by 30 g vitamin C once every 1-2 months for four years. Nine years after diagnosis, the patient is in good health, without signs of disease. Case three was a 66-year-old woman with B-cell lymphoma invading paraspinal muscle and bone at L4-5. She received IV vitamin C 15 g twice weekly for 7 months, then 15 g every 2-3 months for about one year. Ten years after diagnosis, the patient is in good health. Dr. Levine and colleagues note that all three patients survived for longer than expected for the types and stages of cancers that they had. At the doses delivered, vitamin C "is a pro-drug for hydrogen peroxide formation in extracellular fluid," they explain. Histology results also showed evidence of tumour haemorrhage, attributable to ascorbate. The investigators conclude that "the role of high-dose intravenous vitamin c iv therapy in cancer treatment should be reassessed."
[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1405876/]
For further information see Phase 5 of Cancer: Vitamin C Depletion

A SPECIAL TRIBUTE TO VITAMIN C PIONEER, ​DR FREDERICK KLENNER

​Frederick Klenner was a pioneer in the field of using megadoses of ascorbic acid (vitamin C) to treat many illnesses, particularly viral diseases such as polio, in the early 1950's. His leading work and results inspired other forward thinking doctors such as Linus Pauling and Abram Hoffer to treat other illnesseses such as cancer with megadoses of Vitamin C. Abram Hoffer writes: "In the early 1950s, Dr. Fredrick Klenner began his work with megadoses of vitamin C. He used doses up to 100 grams per day orally or intravenously. In clinical reports he recorded the excellent response he saw when it was given in large doses. For example, polio patients given vitamin C suffered no residual defects from their polio. A controlled study in England on 70 children, half given vitamin C and half given placebo, confirmed that none of the ascorbatetreated cases developed any paralysis while up to 20 percent of the untreated group did. This study was not published because the Salk Vaccine had just been developed and no one was interested in vitamins. Dr. Klenner’s work was ignored." Linus Pauling writes: "Dr. Fred Klenner's early research reports provide much information on the use of high-dose vitamin C for the prevention and cure of many diseases, and these reports are still important."

12 Step Cancer Survivor Program

Step 1: Healing the root psycho-emotional cause of cancer

As revealed in the 6 phases of cancer, it is suppressed negative emotions (principally anger, hate, resentment and grief) which cause and continue to fuel cancer at the cellular level. Finding a way to remove these toxic emotions is critical to long term cancer recovery. The 93-page evidence-based thesis, "Psycho-Oncology: The 6 Phases of Cancer", reveals exactly how cancer develops in the body due to the suppression of toxic negative emotions. It is recommended you undertake sessions with an experienced healer of emotions (such as an EFT specialist) who can work with you to permanently remove these toxic emotions. Continuing a daily self-healing program to express and release cancer-causing emotions is also strongly advised and the Cancer Healing Guide is designed for this purpose. The Vipassana meditation technique is also beneficial for releasing toxic emotions. You are also encouraged to explore the link between anger, unforgiveness and cancer and unresolved complicated grief and cancer. The book, "Healing Dis-ease in the Mind of Christ", will help you uncover the spiritual cause of why dis-ease is present. We are aware of illnesses having spontaneously healed during the reading of this book.

Step 2: Systems change (Removing stressful conditions)

As revealed by world-renowned cancer researcher Lothar Hirneise, 100% of all late stage 'miracle' cancer survivors of the hundreds he interviewed had all made dramatic system changes in their life before getting well, and had typically left a highly stressful job or relationship or highly stressful living condition. This is because those diagnosed with cancer have significantly elevated stress hormone cortisol levels, which deplete all-important adrenaline reserves (as outlined in phase 2 of cancer), breaking the cell's Kreb's Citric Acid Cycle, causing cell mutation and cancer. By removing anything in your life that is causing significant stress, this will help to normalize cortisol and adrenaline levels, and thus halt the condition known as cancer.

Step 3: Active relaxing to lower stress cortisol levels

Over many years the typical cancer personality has trained their body to remain rigid and tense in response to life stressors. And when the body is not relaxed the mind will not relax sufficiently enough to enter the deep-sleep-cycle to produce melatonin, which is the primary hormone responsible for inhibiting cancer cell growth. It is this "body stress" which continues to deplete all-important adrenaline reserves in phase 2 of cancer. You should ideally spend 2 hours each day in active relaxation mode to lower stress hormone cortisol levels, which in turn will help restore adrenaline reserves and enable you to enter the deep-sleep-cycle to produce melatonin. Here are some ways to actively relax: sitting amongst nature, walking on the beach, swimming, tai chi, aromatherapy massage, watching funny movies, join a laughter therapy group, holistic pulsing, meditation, deep breathing exercises, lavender oil therapy, and listening to a guided relaxation recording.

Step 4: Using meditation to increase melatonin levels

As revealed in phase 1 of cancer, melatonin is the primary hormone responsible for inhibiting cancer cell growth. It does this by producing interleukin 2 (IL-2) which governs the production of (cancer killing) immune system T cells, B cells, natural killer cells, macrophages and neutrophils. Melatonin is produced in the pineal gland of the brain between the hours of 1am and 3am in the morning during uninterrupted deep sleep. The cancer personality who suppresses for long periods toxic emotions (of anger, hate, resentment, and/or grief) is generally unable to enter this critical deep sleep cycle and therefore becomes depleted of melatonin over time -- one day at a time. Removing the toxic emotions that disrupt deep sleep and lowering stress hormone cortisol levels will naturally correct the problem, however studies have demonstrated meditation can also be used to produce melatonin by stimulating the pineal gland. Consider meditating for 30 minutes per day as part of your 2 hours of daily relaxation.

Step 5: Supporting / boosting the immune system

There are a number of conditions that suppress or weaken the immune system: including high stress hormone cortisol levels, depleted melatonin and dopamine levels, parasites, pathogen microbes (viruses, bacteria, fungus), as well as chemotherapy and radiation. When the immune system is suppressed or weakened, the "cancer fungus" in phase 3 thrives. We recommend you incorporate at least one protocol to support and boost your immune system. High Dose Vitamin C Therapy can be used for this purpose and should wherever possible be used PRIOR to chemotherapy and radiation. Consider also: Fever Therapy, DMG, Lemon Juice Therapy, and Avemar. Note: If you are undertaking chemotherapy or radiation, consider Graviola capsules to prevent side-effects such as hair loss, nausea, and general malaise and energy loss. This natural product also prevents cell-resistance to chemotherapy.

Step 6: Removing the cancer fungus

As revealed by the Holy Spirit of God in phase 3 of cancer, what we know as cancer is in fact seven different types of fungus. When the cancer personality experiences prolonged chronic stress, somatids (tiny microorganisms necessary for life) that live in our body pleomorphise [or change] into yeast-like-fungus to ferment rising glucose and lactic acid in cells. In a healthy person, somatids are limited to 3 stages in their life cycle - somatid, spore, double spore. However, in a highly acidic (low pH) lactic acid environment, somatids pleomorphise into a further 13 stages. These stages include viral-bacterial-yeast-like-fungus forms that: a) migrate to the cell nucleus releasing "mycotoxins" causing cell DNA damage and the mutation of normal cells into cancer cells, and b) ferments the glucose in cancer cells, providing a natural growth factor for cancer and tumor cells to metastasize in the body. For this reason it is recommended you include at least one of the following protocols to remove and keep at bay the cancer-fungus in your body: Apple Cider Vinegar, Garlic, Baking Soda, Essiac Tea, Clarkia, and Hyperthermia.

Step 7: Detoxing the liver and colon of toxins

Those with cancer are typically overloaded with toxins in the key immune system organs of the body: the liver and colon. Toxins include "mycotoxins" or acidic waste products caused by: 1) the cancer-fungus, 2) a poor diet, 3) chemicals, alcohol, tobacco, 4) antibiotics, 5) chemotherapy agents, 6) fermentation of stress hormones, 7) poor exercise regime causing a build-up of lactic acid, and 8) dead microbes, parasites and cancer cells. These toxins build up primarily in the liver -- the master immune system organ. When the liver is overloaded with these toxins, your immune system is weakened and you feel sicker, and cancer and viral-bacterial-yeast-like-fungus thrives. Thus it is very important to have a plan to detox the liver (the master immune system organ), the colon (the intestinal immune system), as well as the gall bladder and kidneys -- especially if you are undertaking a treatment to kill cancer cells or the cancer fungus. If you don't, your liver simply cannot remove all the dead microbes and cancer cells, which remain overloaded in the liver. It is strongly recommended you include a daily treatment plan for detoxing the liver and colon. See Liver-Colon Cleanse for further details. Ozonated Water should be considered also, for it is a superb body detoxifier, but should NOT be used by those with lung cancer or lung conditions.

Step 8: Restoring the Krebs' Cycle with niacin & vitamin C

Cancer can only exist when the Krebs' Citric Acid Cycle of a person's body cells is broken. And this is due to adrenaline depletion (in phase 2), niacin deficiency (in phase 4) and vitamin C depletion (in phase 5), all of which are caused by prolonged chronic stress. Dr Abram Hoffer, the department head of psychiatry at a major hospital in Canada, started using niacin and high doses of ascorbic acid (vitamin C) to treat psychiatric patients and found (by accident) that it also effected a cure in some of his patients with cancer. He subsequently found of 132 patients he treated in his own private practice with advanced stage cancer, 101 patients who followed his program (below) lived on average 16 times longer than the 31 patients who did not or could not follow his program. Dr Abram Hoffer and Linus Pauling presented the following study findings: "Mean survival time for the 31 patients who did not follow the regimen is 5.7 months. Of the others, who did follow the regimen, 20% were poor responders, with mean survival time 10 months, and 80% were good responders, with mean survival time 122 months for 32 patients with cancer of the breast, ovary, cervix, and uterus and 72 months for 47 patients with other kinds of cancer." [Click here to read the full Abram Hoffer/Linus Pauling study and patient survival times.]

Dr Abram Hoffer recommended the following regime to his patients: "The first thing I try to do is to cut their fat way down. So, I put them all on a dairy free program. I reduce, but I don't eliminate, meat and fish, and I ask them to increase their vegetables, especially raw, as much as they can. I think it's a good, reasonable diet, which most people can follow without too much difficulty. Having spent some time with them going over what they ought to eat, I begin to talk about the nutrients. The first one, of course, is vitamin C. The dose is variable. I find that most patients can take 12 grams per day without much difficulty, that's the crystalline vitamin C sodium ascorbate or calcium ascorbate. They take one teaspoon three times per day. If they do not develop diarrhea, I ask them to increase it until this occurs and then to cut back below that level. I think in many cases it would be desirable to use intravenous vitamin C. I also add vitamin B-3, either niacin or niacinamide. I prescribe from 500 mg to 1500 mg per day. I also add a B (vitamin) complex preparation 50 or 100. I think vitamin E is an extremely important anti-oxidant and I use that as well, 800 to 1200 I.U. They also get 25,000 to 75,000 units of beta carotene. I s
ometimes use vitamin A. (One cup of raw carrot juice contains 36,600 units of beta carotene, which converts to vitamin A). I like to use folic acid for lung cancer, and for cancer of the uterus. I use selenium, 200 mcg, three times per day. I use some zinc, especially for prostatic cancers and I do use calcium-magnesium." [Click here to read Dr Abram Hoffer's complete Niacin and Vitamin C Protocol]

[Note: Sourcing the correct ascorbic acid is important. NutriBiotic Ascorbic Acid 100% Pure Vitamin C 5lb from www.iHerb.com appear to offer the best value bulk pharmaceutical grade crystalline ascorbic acid.]

Step 9: Re-alkalizing the body's natural pH balance

As discovered by Otto Warburg, cancer cells only survive in a low pH highly acidic environment, and this is why those with cancer typically have a low pH of between 4.0 and 6.5pH. This highly acidic environment occurs when the Krebs' Citric Acid Cycle of the cell is broken due prolonged chronic stress depleting all-important adrenaline reserves. As the cell can no longer produce ATP energy via the Krebs' Citric Acid Cycle, the cell instead ferments glucose [to obtain smaller amounts of ATP energy] via the process known as Glycolysis, causing lactic acid levels to rise sharply within the cell. This lactic acid problem is further compounded when the somatid in phase 3 of cancer pleomorphises into the cancer-fungus to ferment rising glucose and lactic acid, itself releasing acidic waste products called "mycotoxins". As cancer cells find it difficult to survive in a high pH alkaline environment of 7.5 or greater, it is therefore essential to: 1) Remove the lactic-acid forming psycho-emotional stress (i.e. toxic negative emotions), 2) introduce alkaline-based foods, and 3) include dextrorotatory lactic acid, which is administered in homeopathic form as prescribed by Dr Waltraut Fryda in phase 2 of cancer.

Step 10: Reversing the subconscious desire to "exit life"

As revealed by the Holy Spirit of God in phase 6 of cancer, cancer manifests as a result of a subconscious wanting to "exit life", caused by the individual feeling overwhelmed by the pain of life and no longer having a strong desire or will to live. This desire to exit life -- experienced not so much consciously, but at the subconscious "feeling level" of the mind -- sends subliminal messages to the immune system to shut down and stop working, enabling cancer cells and the cancer-fungus to thrive. God reveals it is important to examine this subconscious desire to exit life and to see whether 2-4 years prior to diagnosis you felt this way, and to make the decision to re-activate the immune system, by generating an energy of wanting to live that is greater than the energy to exit life. The Cancer Healing Guide will help you examine your will to live in greater depth, and of course, removing the toxic negative emotions (emotional pain) that caused the subconscious desire to exit life is a critical key component.

Step 11: Connecting to God / your Higher Spiritual Self

At Puna Wai Ora, we regularly receive messages from God to guide us in the work we are doing. When we asked what is the best late stage alternative cancer treatment available, the first reply we received was prayer. The Angels spoke of the Lord's Prayer spoken out loud daily - preferably in Latin - was the most effective late stage cancer treatment. They indicated it was important to: 1. Ask God for forgiveness of any wrong-doings, 2. Ask God to fill them with white love and light, 3. Ask for the pain to be diminished in Jesus' name [or another spiritual being you pray to], 4. State "Please bless me with white love and light in Jesus' name and let the healing begin", and 5. Thank God, Jesus and the Angels for their healing and your recovery. These are the words of God delivered by the angels: "God will decide if a miracle happens. They need to connect with themselves more that they are on the right path to awareness of spiritual realms and God. They must believe in God to get through, to have more faith and trust in God. Once they open up, they will be open up in more ways than one. Their pain will not be as intense, they will be comforted."

Step 12: Choosing an alternative cancer treatment

It is important to choose at least one alternative cancer treatment to target and eliminate cancer cells within the body. In most cases you should only need to choose one treatment in addition to the above 11 steps. We highly recommend your alternative cancer treatment include at least one dietary treatment such as the Johanna Budwig Cancer Diet, the Gerson Therapy Cancer Diet, the Bill Henderson Diet Protocol (based on the Budwig diet), or the Brandt Grape Cure. The 42 day organic juice fast known as the Breuss Cure or Breuss Treatment has also been used in the treatment of cancer. Remember, always choose a diet you enjoy that fosters a will to live. To view a list of further treatment options, see: Alternative Cancer Treatments.  

Healing Dis-ease in the
​Mind of Christ

This new revelation from God reveals the spiritual cause of why dis-ease is present. It is available freely in pdf format, and is also available at Amazon.

Picture

Psycho-Oncology: The 6
Phases of Cancer

This 93-page evidence-based thesis reveals exactly how cancer develops in the body over 6 separate phases. It is freely available in pdf format.

Picture

Who survives cancer?
​By Lothar Hirniese

After interviewing hundreds of miracle 'late-stage' cancer survivors, world-renowned cancer researcher, Lothar Hirneise, reveals the 3 most important steps they took to survive.

Picture

God reveals Cancer is
​seven types of fungus

In this extraordinary revelation, the Holy Spirit of God reveals cancer is in fact seven different types of fungus. The Holy Spirit of God also reveals the two natural remedies for reversing this disease at the outer physical level.


God reveals the cancer-fungus is caused by a subconscious wanting to "exit life"

In a further extraordinary revelation, the Holy Spirit of God reveals cancer is caused by a subconscious wanting to "exit life". Healing the mind-body-spirit is thus a crucial step to fostering a will to live.


Glen Russell: The weed that is cancer must be cut off at the root, to ensure it does not regrow. Many cut off the top of the weed (what we see at the surface) by taking physical remedies; but the root of the dis-ease, the spiritual and mental dis-ease, is often left behind.

Restoring the Krebs' Citric Acid Cycle: A two-pronged approach

As the patient makes a sustained effort to cut off the root of the cancer weed (the spiritual and mental dis-ease), this will begin the process of normalising the Krebs' Citric Acid Cycle naturally, through the normalisation of adrenaline levels and niacin and vitamin C levels. Yet this takes time. And if the cancer has progressed to such a point, that as revealed by God in phase 6 of Cancer may be difficult to reverse, the approach taken by Dr Abram Hoffer and Linus Pauling in Step 8 (below) demonstrates that even in a high percentage of late-stage cancer patients, long term survival is possible using simply this outer physical "Krebs" approach. An analogy one could equate is such: The house is on fire (the cancer in the body) and all the conditions for creating the fire are in the process of being removed (in steps 1-4), yet the fire still burns. So a two-pronged approach is often necessary to both contain and stamp out the existing fire, while at the same time removing all conditions that could restart the fire anew.


Dr Lorraine Day's experience with the Gerson Therapy

Dr Lorraine Day, former Chief of Staff of Orthopedic Surgery at San Francisco General Hospital, reveals how after using the Gerson Therapy Cancer Diet for 8-9 months to cure her cancer, without addressing the root underlying psycho-emotional cause, that the cancer came back even more aggressively.

Picture

About this
​Program

The 12 Step Cancer Survivor Program has been prepared by Glen Russell of Puna Wai Ora Mind-Body Cancer Clinic. It points to critical areas to be considered when one is seeking to reverse the 6 phases of cancer outlined in Psycho-Oncology: The 6 Phases of Cancer.

FAQ

1. Is it necessary to include all 12 steps in this program?

The answer is no. For example, you may address healing the root psycho-emotional cause of cancer (in Step 1) and do this successfully, and combine this with killing the cancer fungus (in Step 6), or with restoring the Krebs' Citric Acid Cycle (in Step 8). If you restore the Krebs' Citric Acid Cycle, this automatically prevents normal cells mutating into the cancer fungus, so in effect Step 6 would not be necessary; although you can do both (Step 6 and Step 8) to super-charge the effect.

Similarly, you could combine Step 1 with a cancer diet (such as the Gerson Therapy Cancer Diet) in Step 12. Both of these steps contribute to eliminating the cancer fungus (in Step 6) and also contribute to normalising pH acid/alkaline levels (in Step 9). Step 1, that is the healing of the root psycho-emotional cause of cancer, also contributes to normalising melatonin, adrenaline and stress hormone cortisol levels, so steps 2-4 are not crucially important if you are already implementing Step 1 correctly.

Deciding which steps to include comes down to personal choice; for not every step of this program is either suitable or well-tolerated; and some of the therapies may present as a contraindication to a patient with a pre-existing condition (such as ozone water should not be consumed by those with lung disease or lung cancer). With that said, one could certainly do all 12 steps of this program (which predominantly are natural therapies) under the supervision of their doctor.

2. Should I undertake chemotherapy / radiation while on this program?

The 12 Step Cancer Survivor Program includes therapies which generally fall under the category of "complementary and alternative medicine" or CAM. For the most part, these therapies support the immune system and the healing process during harsher treatments, such as chemotherapy and radiation. For example, vitamin C is known to protect the immune system during chemotherapy, and hyperthermia is known to increase the effectiveness of radiation.

While there is some anecdotal evidence of survival rates being greater amongst those who do both mainstream medicine and CAM, deciding whether to undertake chemotherapy and radiation remains always a personal choice.

It must also be stressed that Linus Pauling concluded in his research that the effectiveness of high-dose vitamin C was not as effective if used AFTER chemotherapy, versus prior to chemotherapy.

3. Do people recover from cancer on this program?

A number of individuals with late stage cancer who have worked one-on-one with Glen Russell to heal the root psycho-emotional cause of cancer (in Step 1) have entered into complete remission within 2 weeks of having completed their sessions. Some of these patients, including two medical doctors, are mentioned as case studies in Psycho-Oncology: The 6 Phases of Cancer. This, however, does not mean the cancer could not return if the patient does not change their mental outlook, and "re-creates" the psychological conditions that leads to a new bout of cancer.

Apart from these cases who have worked one-on-one with Glen, it is difficult to ascertain the effectiveness of this program, as many combine this program (or parts of it) with other alternative or mainstream therapies.

Vertical Divider
Discover how lavender oil therapy is being used around the world to lower stress hormone cortisol levels and overcome depression and insomnia.
Picture

​Program S​upport

Psychoneuroimmunology expert Glen Russell of Puna Wai Ora Mind-Body Cancer Clinic offers free guidance and support for those seeking to reverse the 6 phases of cancer. If you have a question for Glen, please fill in the form below. Glen will contact you as soon as he is able.
Submit

HEALTH DISCLAIMER
Puna Wai Ora Mind-Body Cancer Clinic is an expert in the field of mind-body cancer therapy only. Although Puna Wai Ora Mind-Body Cancer Clinic has compiled research findings on alternative cancer treatments included in this website, it does not claim to be an expert in these fields or to have medical or professional expertise in these fields. Puna Wai Ora Mind-Body Cancer Clinic encourages each person reading the information contained in this website to draw their own conclusions as to the potential benefits of each complementary and alternative cancer treatment and alternative cancer therapy listed and to seek medical advice from their medical doctor and/or cancer specialist or oncologist before undertaking any such therapy.
Picture
Puna Wai Ora Mind-Body Cancer Clinic, 2006-2023
Contact Us I Site Map

  • Phase 1 of Cancer: Inescapable Shock
  • Phase 2 of Cancer: Adrenaline Depletion
  • Phase 3 of Cancer: The Cancer Fungus
  • Phase 4 of Cancer: Niacin Deficiency
  • Phase 5 of Cancer: Vitamin C Depletion
  • Phase 6 of Cancer: Immune Suppession
  • Cancer-Grief Link
  • Cancer-Anger Link
  • Cancer-Fungus Link
  • Beating Cancer with Nutrition
  • Dr Ryke Geerd Hamer
  • EFT and Cancer
  • EMF Radiation and Cancer
  • Essiac Tea and Cancer
  • Fever Therapy and Cancer
  • Garlic and Cancer
  • Gerson Therapy Cancer Diet
  • God Cancer Cure
  • High Dose Vitamin C Cancer Treatment
  • Whole Body Hyperthermia Cancer Treatment
  • Johanna Budwig Cancer Diet
  • Cancer and Detoxing the Liver
  • Melatonin, Meditation and Cancer
  • Niacin Vitamin B3 and Cancer
  • Oxygen Ozone Cancer Therapy
  • Photodynamic Therapy for Cancer
  • Prayer, God and Cancer
  • Acid-Alkaline pH and Cancer
  • Who Survives Cancer?
  • Baking Soda (Sodium Bicarbonate) and Cancer
  • Massage, Cortisol and Cancer
  • The Brandt Grape Cure and Cancer
  • Cesium Chloride Cancer / DMSO
  • MMS Cancer
  • MMS Cancer Study
  • MMS Cancer Testimonials
  • Overnight Cure for Cancer
  • Avemar Cancer Treatment
  • Hulda Clark Parasite Cancer Cleanse: Clarkia
  • DMG Cancer Immune System
  • Vipassana Meditation and Cancer
  • Guided Relaxation for Cancer
  • Lavender Oil Therapy for Cancer
  • The Cancer Healing Guide