Cancer Fungus: The Link Between The Microbe And Cancer

CANCER FUNGUS: THE LINK BETWEEN THE MICROBE AND CANCER

The cancer fungus link is well-documented. Fungus is a microbe, and many scientists believe viruses, fungus and bacteria are all different stages of the microbe life cycle. The microbe has long been associated with and identified as a possible cause for cancer. A large and significant number of independent cancer researchers, scientists, micro-biologists and prominent medical practitioners over the past 100 years [as shown below] have found overwhelming evidence supporting this cancer fungus link or link between cancer and the microbe. They have also discovered and observed that this microbe is pleomorphic, meaning it changes back and forth from harmless spore form to harmful viral, bacterial and yeast-like fungus form. This microbe, they found, is always present in cancer/tumor cells.

1890

On December 3, 1890 William Russell, a pathologist in the School of Medicine at the Royal Infirmary in Edinburgh, gave an address to the Pathological Society of London in which he outlined his histopathologic findings of a characteristic organism of cancer that he observed microscopically in fuchsine-stained tissue sections from all forms of cancer that he examined, as well as in certain cases of tuberculosis, syphilis and skin infection. The parasite was seen within the tissue cells (intracellular) and outside the cells (extracellular). The size of Russell's parasite ranged from barely visible, up to "half again as large as a red blood corpuscle." The largest round forms were easily seen microscopically. The large size of some of these bodies suggested a fungal or yeast-like parasite. Russell provisionally classified the parasite as a possible "blastomycete" (a type of fungus); and called the forms "fuchsine bodies" because of their bluish-red staining qualities.

1901

After three years work at the New York State Pathological Laboratory of the University of Buffalo, Harvey Gaylord confirmed Russell's research in a 36-page report titled "The protozoon of cancer", published in May, 1901, in the American Journal of the Medical Sciences. Gaylord found the small forms and the large sacs characteristic of Russell bodies in every cancer he examined. Some large spherical bodies were four times the diameter of a leukocyte (white blood cell). Red blood cells measure about 7 micron in diameter and leukocytes are 2 to 3 times larger than red blood cells. Thus, some of the bodies that Gaylord observed attained the amazing size of around 50 micron in diameter. In addition, he found evidence of internal segmentation within the larger bodies "after the manner recognized in malarial parasites." The tiniest forms appeared the size of ordinary staphylococci.

1920

In the 1920s James Young, an obstetrician from Scotland, repeatedly grew pleomorphic bacteria from various cancers. The microbes had a "specific life cycle" and "spore stages" comprised of exceedingly tiny and barely visible spores. In the laboratory these tiny spores transformed into larger coccoid (round) forms, rod-forms and yeast-like forms (similar in size to Russell bodies). Young found his microbe in 16 cases of breast cancer, and in two mice with breast cancer. He identified "spore forms" and clumped "spore balls" in microscopic sections prepared from the mouse tumours.

1925

In 1925 Northwest Medicine published two papers by Michael Scott, a Montana surgeon who learned about the cancer microbe in TJ Glover's lab in 1921. Scott's microbe was similar to Young's. The parasite had a life cycle composed of three stages: a coccus, a rod, and a "spore sac" stage. Scott believed cancer was an infection like tuberculosis and attempted a vaccine treatment, but his treatment methods were quickly suppressed by the medical establishment.

In 1925, John Nuzum, a pathologist and physician at the University of Illinois College of Medicine, reported a pleomorphic coccus he repeatedly isolated from breast cancer. The tiniest forms were virus-like and passed through a filter designed to hold back bacteria. Nuzum grew his "micrococcus" from 38 of 41 early breast cancers, and from the cancerous lymph nodes and metastatic tumours resulting from spread of the cancer to other parts of the body. During his 6 years of intensive bacteriological study, he learned the microbe could pass through a filter designed to hold back bacteria, indicating that some forms of the microbe were as small as the size of some viruses. With special stains he detected these small round coccoid forms within the breast cancer tumour cells. Although Nuzum couldn't produce cancer tumours in mice, he was able to induce breast cancer tumours in 2 of 5 dogs injected with the microbe.

1932

Royal Raymond Rife studied medicine at the prestigious John Hopkins University, and began his career as a research pathologist and medical researcher. Over his lifetime, Rife was to receive fourteen major scientific awards and honours and an honorary doctorate from the University of Heidelberg for his scientific discoveries. Royal R. Rife cultured tissue from a breast cancer sample, in Kendall medium, and isolated a micro-organism. He followed this experiment with a series of other studies in which he cultured an organism in Kendall media, from tissue taken from a human breast cancer. He then injected this microorganism into 412 healthy rats, and found that without fail they all developed breast cancer. Finally, he was then able to isolate the original microorganism from the tumours which grew in the rats. In the process Rife became probably the first person ever to fulfil Koch's postulants, for cancer causing microbes. Koch's Postulants are a set of rules to prove the causation of disease by microorganisms. They state that to prove such causality the microorganism must first be isolated and cultured. It must then be shown to have infected a health animal, and finally the same organism must be recoverable from the now infected animal. The cancer virus which Rife named Cryptocides Primordiales or the BX virus, was a minute 1/5 micron in length and 1/20 micron in width. It was highly motile, aerobic (requiring free oxygen for its survival) and highly pathogenic. Rife discovered that while exposing the virus to a temperature of 42C for 24 hours would kill the virus, it remained unaffected by exposure to either X-ray, UV or Infra-red waves. While the discovery of a cancer virus was in itself an incredible feat of scientific endeavour, Rife was to make yet more discoveries destined to rock the scientific status quo. The BX virus was shown to be a polymorphic virus, able to change its states according to the culture in which it was grown. When a BX virus was cultivated in a different media, it was seen to change into a BY virus. When the media was changed yet again it developed into a monococcoid in the monocytes of the blood, and with a further change of media it morphed once again, this time into crytomyces pleomorphia fungi. At any stage along this journey of polymorphism, the original BX virus could be grown again by adding any one of these forms to the original media.

1935

Another pleomorphist, Canadian researcher of Dr Gruner was watching Rife's work with interest. Gruner was using asparagus agar to grow fungus from cancer blood. Rife was growing a virus from cancer tissue using Kendall media. In the 1930's both Gruner and Rife collaborated and went on to discover that when a sample of Gruner's fungus was cultured on K media the BX virus emerged. By changing the media they could turn a fungus originally grown out of cancer blood into the BX organism, itself grown out of cancer tissue. They repeated this experiment hundreds of times with exactly replicable results each time.

1940

Virginia Livingston, independently discovered the cancer microbe in the late 1940s. Aided by micro-biologist Eleanor Alexander-Jackson, who supplied the bacteriologic expertise, the two women found a special stain (the acid-fast stain) that allowed the microbe to be recognised in culture and within the cancer tumour. Like the researchers back in the 1920s, they confirmed the microbe was filterable; and electron microscopic photos provided further proof that the filterable forms were indeed viral-size. Livingston has written three books on the cancer microbe: Cancer: A New Breakthrough (1972), The Microbiology of Cancer (1977), and The Conquest of Cancer (1984).

1950

In the 1950s Irene Diller of the Institute for Cancer Research at Fox Chase, Philadelphia, discovered fungus-like microbes in cancer cells. Joining forces with the Livingston team, Diller worked with specially bred mice with a proven cancer incidence. By injecting them with microbes cultured from breast cancer and other tumours, she was able to more than double the cancer incidence of the mice. She injected healthy animals with cancer bacteria. When cancer tumours developed she successfully cultured the microbe from the tumours - thus proving that these bacteria were implicated in the production of cancer. Utilising Livingston's methods, Diller also grew the microbe from the blood of cancer patients.

1950 - PRESENT

In the 1950, Professor Gaston Naessens invented a high-powered light microscope, capable of viewing the tiniest forms of life within blood. With this microscope, Naessens discovered in the blood of animals and humans – as well as in the saps of plants – a subcellular microscopic life form that reproduces, which he christened a somatid (tiny body). The somatid, he found, could be cultured (grown) outside the bodies of its hosts (in vitro, "under glass,"). Naessens also observed that this somatid life form was pleomorphic (form-changing). He observed this somatid life form was limited to 3 stages in a healthy organism – somatid, spore, and double spore – and that these 3 stages where crucial to the organisms survival. What was more amazing, was that Professor Naessens observed that this somatid life form became pathogenic (harmful) when the immune system of the organism was compromised or weakened. He observed these somatid life forms then entered a further 13 stages of development, changing from bacterial into yeast-like fungus forms. (A total of 16 stages). Naessens studied the blood of various degenerative diseases, including rheumatoid arthritis, multiple sclerosis, lupus, AIDS, and cancer, and consistently found the 16 stages of the somatid life cycle (shown below) present in all of these diseases.

1960 - 1990

In the early 1960s Florence Seibert became so impressed with Irene Diller's research that she quit retirement to help prove that bacteria cause cancer. Back in the 1920s Seibert devised a method to make intravenous transfusions safe by eliminating contaminating ubiquitous bacteria. Later, as one of the foremost authorities investigating the chemistry and immunology of the acid-fast bacteria that cause tuberculosis, she perfected the skin test for tuberculosis that has been used worldwide ever since. In 1938, she was awarded the famed Trudeau Medal, the highest prize given to tuberculosis research. Experiments conducted by Seibert and her research team showed these acid-fast and TB-like cancer microbes were not laboratory contaminants because they were able to isolate bacteria from every piece of tumour (and acute leukemic blood) they studied.

1983

In 1983, Cosmic Awareness – the force that expressed itself through Jesus of Nazareth, the Buddha, Krishna, Mohammed, Edgar Cayce, and others who served as spiritual messengers for God – reveals cancer is indeed a fungus. In this revelation, it is revealed that there are seven different types of fungus which are diagnosed as cancer. In this revelation, it is also revealed that Apple Cider Vinegar together with High Dose Vitamin C or equivalent amounts of lemon juice can effectively rid this cancer fungus from the body. To read this full article, click on Lemon Vinegar Cancer Treatment.

1983 - PRESENT

Dr Tullio Simoncini is an Italian doctor specialising in oncology, diabetology and in metabolic disorders. He has treated and cured many cancer patients with sodium bicarbonate (the strongest anti-fungal chemical known to man), commonly via catheter, and has observed tumours consistently disappear within weeks. His book, “Cancer is a Fungus – The Revolution in the Therapy of Tumours” is widely available. It is Dr Simoncini’s unequivocal belief that cancer and tumours are the result of fungal growth in the body, supporting the cancer fungus link. [Note: Injecting baking soda into the body may cause side effects]. See: Sodium Bicarbonate Cancer Treatment

WORLD HEALTH AUTHORITIES LINK THE MICROBE TO CANCER

1. "The over representation of cancer in a region where there is a high incidence of parasitic disease, and the unique characteristics of bilharzial bladder cancer, indicate the possibility that this parasite plays a role in the etiology of cancer. The presence of chronic bacterial cystitis, complicated by urethral strictures, calculi, diverticulae and paralytic stasis, has been known to induce epithelial changes in the bladder mucosa, which may progress to invasive cancer." [CA: A Cancer Journal for Clinicians, the American Cancer Society - Parasites in the Etiology of Cancer: Bilharziasis [parasite] and Bladder Cancer, 1977, Dr. Elsebai, Professor of Surgery, Cancer Institute, Cairo University, Egypt.

2. "Schistosomiasis (also known as bilharziasis), an infection with a parasitic worm called Schistosoma hematobium that can get into the bladder, is also a risk factor for bladder cancer. Although this parasite is found mostly in Northern Africa, it does cause rare cases of bladder cancer in the United States among people who had been infected by the worm before moving to this country." [American Cancer Society]

3. According to the US National Cancer Institute, "Being infected with parasites increases the risk of bladder cancer." It is possible that the immune system in a highly parasitized human being is compromised. In attempting to fight off the large amounts of [foreign] parasites, cancer cells that exist in every human being are left alone to multiply - the immune system simply not having enough resources to go around.

4. The World Health Organization estimates over 1.5 million of the total of 10 million new cancer cases a year could be avoided by preventing the infection associated with them. WHO states that "Viruses, bacteria and parasites emerge as the "secret agents" causing millions of cases of cancer" each year.

5. Many cancers are associated with infections (for example, cervical cancer is linked to the human papilloma virus), but there is no stronger link between a human malignancy and a parasitic infection than that between cancer of the bile ducts and a liver fluke called Opisthorchis viverrini. Scientists at the Queensland Institute of Medical Research (QIMR) in Brisbane are part of an international study into the link between cancer and a parasite found in South-East Asia. The institute’s Dr Alex Loukas says bile duct cancer is prevalent in Thailand and Laos, where people eat raw fish. He says the results could be applied to other cancers caused by parasites. "We know from collaborations with our colleagues in Thailand that the cancer is highly likely to be caused by proteins that this worm secretes into the bile ducts as part of its feeding process".

6. [American Cancer Society] "Cervix cancer is caused by a virus called HPV. HPV is short for human papilloma (pap-ah-LO-mah) virus. This virus can cause changes in the cervix. HPV is NOT the same as HIV. HPV is not a new virus, but we are learning more about this virus. Almost everyone who has ever had sex has had HPV at some time in his or her life. HPV is spread through sex and it can cause an infection in the cervix. The infection usually doesn't last very long because your body is able to fight the infection. If the HPV doesn’t go away, the virus may cause cervix cells to change and become pre-cancer cells."

7. The Institute for Genomic Research and the International Livestock Research Institute have joined forces to decode the DNA of one of Africa’s most destructive cattle parasites. East Coast Fever is caused by a protozoan parasite carried by ticks. The parasite is known to scientists as Theileria parva. Once injected into the cow’s bloodstream it invades the animal’s white blood cells, causing them to divide uncontrollably, like cancer cells. The multiplying cells clog the cow’s organs, killing the animal within 2 to 4 weeks. Knowledge of the genes that the parasite uses to start this lethal cell division may shed light on the mechanisms that cause human tumours to grow. Research on the East Coast Fever parasite has already led to the identification of a previously unknown mechanism that causes leukemia in mice.

8. A new study links parasites with immunosuppression. Stool specimens taken from 38 children with malignancy and from 92 healthy children were investigated for intestinal parasites. The 38 children with malignancy had lymphoma or leukemia and were considered immunosuppressed. Several different parasites were found in 16 of the 38 patients with immune deficiency (47.3%), compared to only 16 of the 92 healthy children (17.3%). The incidence of parasites in patients with malignancy who were immunosuppressed was significantly higher than in the healthy control group. [Study performed by Department of Parasitology, Dokuz Eylül University Faculty of Medicine, Ýzmir, Turkey and Behçet Uz Children's Hospital, Ýzmir, Turkey, March 2004].

12 STEP CANCER SURVIVOR PROGRAM

STEP 1: HEAL 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" (freely available below), reveals exactly how cancer develops in the body over 6 separate phases. Here you will be given proof from many hundreds of universities from around the world how cancer is caused due to the suppression of toxic negative emotions, and how this occurs at the cellular level. 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 uncovering and releasing toxic emotions. You also encouraged to explore more fully the link between anger, unforgiveness and cancer and unresolved complicated grief and cancer. The book, "Healing dis-ease in the Mind of Christ" (also freely available below), will help you to explore more deeply the spiritual cause of why dis-ease is present within the mind, the spirit and the physical body.

Psycho-Oncology: The 6 Phases of Cancer reveals how cancer occurs in the physical body due to a chronic stress build-up of unresolved trapped negative emotions.

Click here to view, print or download

Healing dis-ease in the Mind of Christ reveals both the spiritual cause and remedy of dis-ease in the mind, which manifests as dis-ease in the physical body.

Click here to view, print or download

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 within the body 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 which is fuelled by chronic stress.

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 "rigidity of body" that adds to the internal 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, 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 things 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 really works and 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 damaga 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 cannot remove all the dead microbes and cancer cells, which remain overloaded in the liver. We recommend you include a daily treatment plan for detoxing the liver and colon. See Liver-Colon Cleanse. Ozonated Water should be considered 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 so-called 'incurable 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 full Abram Hoffer/Linus Pauling study and what each patient took to survive.]

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. (One cup of raw carrot juice contains 36,600 units of beta carotene, which converts to vitamin A). I sometimes use 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 for the best value bulk pharmaceutical grade crystalline ascorbic acid. PDF view/download: Niacin and Vitamin C Protocol

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.

STEP 10: REVERSING THE SUBCONSCIOUS DEATH WISH

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 suppressed 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.

RACHEL'S STORY: A STORY OF HOPE & HEALING

Rachel Lynn Sebastian is an international recording artist who was diagnosed with infiltrative ductal carcinoma in 2015. Rachel shares her story of hope and healing and offers a way forward for you to heal within ... [Click here to read more]

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.

Puna Wai Ora Mind-Body Cancer Clinic is a subsidiary of The Leighton Crichton
Church of Jesus Christ of Latter Day Saints, 2006-2020
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