"For some reason modern medicine has itself turned a corner and entered a darkness and is now committing crimes against humanity unequalled
in the history of our race."
 
--Dr. Mark Sircus
NATURAL HEALING 
featuring 
Alternative Cancer Treatments

INTRODUCTION: by DIANNE JACOBS THOMPSON (under construction)
1979 Around January of that year, I went home to die.   ..cont. 
I was diagnosed with stage 2 stomach cancer, chronic bronchitis, acutely infected ovarian cysts, arthritis, sciatica, low thyroid, anemia and a heart condition. Besides that I had chronic ear infections and long-standing clinical depression. The late Dr. Harold Dick, N.D., known as a "naturopathic oncology pioneer" cured me in 5 weeks. It required the diagnosis (the Carroll Food Test) of digestive enzyme deficiency food intolerances which most people have and few know about, and it also identified the primary tissue salt deficiency, along with treatment with glandular protomorphogens to restore glandular health, and Constitutional Hydrotherapy to bring about detoxification, to stimulate blood circulation and the activity of the vital organs and to jump-start the immune system. It turned out to be the basic foundation of the most successful healing system I've ever witnessed.
1986 My 5-year-old daughter was forcibly vaccinated and immediately developed a flesh-eating infection so virulent that my husband and I became infected from contact. Naturopathic medicine brought us back from the brink.
Later that year we were introduced to escharotic cancer salves and treated a dog tumor, my husband's cirrhosis of the liver, various skin lesions, moles, fungal infections, and a lump in my thigh. It eventually helped clear up the remaining symptoms from my husband's flesh-eating infection after he was forced to submit to antibiotic treatment which made a mess of it. There was much more, gallbladder problems in 1999, adrenal deficiency 2001, injury in 2002, arthritis, diabetes, and other issues between 2003-2012, including glaucoma--cured.

This is why I research and write about alternative medicine. It's a debt.

Please help support this website by purchasing hand-fired glass beads and jewelry at nitabeads1 to assist in covering the costs of books, reports, & articles needed for continuing research.


 

 

 

 


 

 

 


*
Alternative treatments for cancer, chronic-degerative disease, infection, stress, harmful emotions and other disorders and conditions;
*Information about junk science and bad medicine, including unsafe and ineffective vaccines and undiagnosed medical conditions mimicking child abuse and Shaken Baby Syndrome;

Natural Healing Information
This site provides starting points. The rest of the journey must be yours.

"Truth wears no mask, seeks neither place nor applause, 
bows to no human shrine; she only asks a hearing"


SUBJECT: "CANCER" BY DR. MARK SIRCUS

http://www.oceanplasma.org (academic site)
http://www.oceanplasma.com (orders & requests)

ocean plasma (seawater) website article
Miracle From The Sea--Nexus article, earlier drafts
Seawater as blood plasma substitute (Nexus Article)
Seawater article rough drafts and notes
The Marine Treatment photos (old photos from the French medical archives)
Marine Treatment (Ocean Plasma) 2, at home
Dr. Mark Sircus "Medical Miracle From the Sea"
Seawater solids save sacred Indian Buffalo lands


http://www.imva.info

http://www.magnesiumforlife.com

The following report comes from a membership site: http://www.holisticcancersolutions.com There is a $67 membership fee which opens up the site for all of the many reports contained within. Before that, a summary of the reports is available for anyone to read, to see if it looks like information they want. It is well worth the investment, but for those who can't afford to pay, one can contact the site manager and request special circumstances for free access. They do not intend on withholding potentially life-saving information from anyone who needs it. For those who can pay, there is even a money-back policy within a time frame.

When I first joined this site several years ago, the fee was $97, so they have reduced the price.

Sodium Bicarbonate
Report #3
Sodium bicarbonate
(pharmaceutical grade baking soda)

The latest news in cancer therapy comes from Italy. An oncologist in Rome, Italy, Doctor Tullio Simoncini, is destroying cancer tumors with sodium bicarbonate. S. b. is safe, inexpensive, and extremely effective as an anti-cancer agent.

" It’s an irresistible chemical, cyanide to cancer cells, for it hits the cancer cells with a shock wave of alkalinity, which allows much more oxygen into the cancer cells than they can tolerate. Cancer cells cannot survive in the presence of high levels of oxygen. Sodium bicarbonate is, for all intent and purposes, an instant killer of tumors." (http://www.nutrimedical.com/)

Sodium bicarbonate is a chemical compound with the formula NaHCO3. Sodium bicarbonate (baking soda) is commonly used as an antacid for short-term relief of stomach upset, to correct acidosis in kidney disorders, to make the urine alkaline during bladder infections and to minimize uric acid crystallization during gout treatment. Prescription sodium bicarbonate products are given by injection to treat metabolic acidosis and some drug intoxications. Sodium bicarbonate is available as a nonprescription medical as well as a general house hold item. It is also used with other non-prescription drugs for short-term treatment of various conditions to treat anything from fever to moderate pain.

Writes Dr. Simoncini:

The fundamental reason and the motives that suggest a therapy with sodium bicarbonate against tumours is that, although with the concurrence of a myriad of variable concausal factors – the development and the local and remote proliferation of these tumours has a cause that is exclusively fungin.

At the moment, against fungi there is no useful remedy other than, in my opinion, sodium bicarbonate. The anti-fungins that are currently on the market, in fact, do not have the ability to penetrate the (tumor) masses ... since they are conceived to act only at a stratified level of epithelial type. They are therefore unable to affect myceliar aggregations set volumetrically and also masked by the connectival reaction that attempts to circumscribe them.

We have seen that fungi are also able to quickly mutate their genetic structure. That means that after an initial phase of sensitivity to fungicides, in a short time they are able to codify them and to metabolise them without being damaged by them – rather, paradoxically, they extract a benefit from their high toxicity on the organism.
This happens, for example, in the prostateinvasive carcinoma with congealed pelvis. For this affliction, there is a therapy with anti-fungins which at first is very effective at the symptomatological level but through time it consistently loses its effectiveness.

Sodium bicarbonate, instead, as it is extremely diffusible and without that structural complexity that fungi can easily codify, retains for a long time its ability to penetrate the (tumor) masses. This is also and especially due to the speed at which it disintegrates them, which makes fungi’s adaptability impossible, thus it cannot defend itself. A therapy with bicarbonate should therefore be set up with strong dosage, continuously, and with pauseless cycles in a destruction work which should proceed from the beginning to the end without interruption for at least 7-8 days for the first cycle, keeping in mind that a mass of 2-3-4 centimetres begins to consistently regress from the third to the fourth day, and collapses from the fourth to the fifth.

Generally speaking, the maximum limit of the dosage that can be administered in a session gravitates around 500 cc of sodium bicarbonate at five per cent solution, with the possibility of increasing or decreasing the dosage by 20 per cent in function of the body mass of the individual to be treated and in the presence of multiple localisations upon which to apportion a greater quantity of salts.

We must underline that the dosages indicated, as they are harmless, are the very same that have already been utilised without any problem for more than 30 years in a myriad of other morbid situations such as:

* Severe diabetic ketoacidosis
* Cardio-respiratory reanimation
* Pregnancy
* Haemodialysis
* Peritoneal dialysis
* Pharmacological toxicosis
* Hepatopathy
* Vascular surgery

The discovery of Dr. Simoncini is that sodium bicarbonate is lethal to fungi. Why is that so significant for the cancer patient?

A cancer cell survives by a fermentation-based metabolism. Where there is fermentation, there is yeast, that is, fungus. Remember: "In every very sick cancer cell resides a very healthy fungal microbe." It is the fungus that keeps the cancer cell alive.

If we want to kill the fungus - or fungal colony - in the cancer cell, we want to lead the sodium bicarbonate into the cancer cell. How can this be done?

It can be done surgically, by creating an arterial map to show the blood vessels that directly feed into the tumor; then a catheter can be inserted into the appropriate vein, and a solution of sodium bicarbonate can be injected into it. This is the hard way.

The easy way is to use a trojan horse that will carry the sodium bicarbonate straight into the cancer cells. Two methods are available, suggested by the author of this web site. One is insulin potentiation. The insulin makes the cancer cells starved for sugar, then a glucose solution, mixed with a sodium bicarbonate solution, is infused intravenously. The cancer cells greedily absorb the glucose/sodium bicarbonate solution, which will destroy the fungus in them instantly. To my best knowledge, the method has not yet been used anywhere.

An easier and simpler way is to mix DMSO with the sodium bicarbonate solution, and apply it intravenously. The DMSO will bond with the sodium bicarbonate, and lead it straight into cancer cells, because DMSO seeks out cancer cells selectively. This is a safe and inexpensive protocol. The first clinic that is introducing this brand new therapy in the USA is the CAMELOT CANCER CARE LLC clinic in Tulsa, Oklahoma. As of June 2, 2007, the preliminary results of this protocol are extremely encouraging.

Finally, for the cancer patient who is seeking self treatment at home, there is a third method. DMSO is a superb penetrator. It is so effective that it can be argued that applying DMSO topically, on large surface areas of the skin, it will enter the organism more effectively than by swallowing it, because this way it avoids the gastric juices of the stomach and infiltrates tissues and organs directly. The cancer patient can topically apply a DMSO/sodiumbicarbonate solution as often as he/she wants. The treatment is inexpensive, relatively simple and safe. However, no cancer treatment, no matter how safe and simple, should be carried out without consulting an expert guide. If you wish to use this method, ask your holistic doctor whether you need special injectable pharmaceutical grade sodium bicarbonate, and if so, where to get it.

Both DMSO and sodium bicarbonate will pass the blood/brain barrier; the above described methods can be used by brain tumor patients.

The solution will also penetrate bone structures, if the cancer is in the bone marrow, like in case of leukemia.

Please keep in mind that an intravenous application is always on a much higher level as far as efficacy goes than topical, oral or injected treatment. However, if the patient has no access to intravenous therapy, the topical application of DMSO/sodium bicarbinate is a very promising one.

Is it a known and proven fact that sodium bicarbonate has powerful anti-fungal properties? Here are some examples:

Sodium bicarbonate (baking soda) as fungicide:
Cornell University scientists demonstrated significant control of powdery mildew and black spot by weekly spraying of 0.063M aqueous solution of baking soda.

United States Patent 6432425
http://www.freepatentsonline.com/6432425.html
Abstract:
A formulation consisting of sodium bicarbonate, sodium carbonate and trisodium phosphate in aqueous solution is applied topically to treat an array of skin and tissue problems. The solution offers antibacterial, antiseptic, anti-fungal, and healing properties to skin scratches, cuts, sores, and fungus-infected nails. In addition, the solution dries as a thin film to the applied surfaces, continuously providing antibacterial, anti-fungal and antiseptic activity beneath the protective film long after it has been applied.

United States Patent 5518727
http://www.freepatentsonline.com/5518727.html
Abstract:
This invention provides alkali metal bicarbonate powder consisting of a narrow size distribution range of ultrafine particles. The ultrafine powder has a large surface area, and provides enhanced reactivity in applications such as deodorization or neutralization, and exhibits increased antibacterial/antifungal activity.

Sodium bicarbonate is widely used in gardening and agriculture as a benign, non-toxic general antifungal and pesticidal agent.


Magnesium and Cancer
Magnesium and Cancer

International Medical Veritas Association

Magnesium stabilizes ATP[i], allowing
DNA and RNA transcriptions and repairs.[ii]

There is a power and a force in magnesium that cannot be equaled anywhere else in the world of medicine. There is no substitute for magnesium in human physiology; nothing comes even close to it in terms of its effect on overall cell physiology. Without sufficient magnesium, the body accumulates toxins and acid residues, degenerates rapidly, and ages prematurely. It goes against a gale wind of medical science to ignore magnesium chloride used transdermally in the treatment of any chronic or acute disorder, especially cancer.

Magnesium repletion produced rapid disappearance of the periosteal tumors.[iii]

Aleksandrowicz et al in Poland conclude that inadequacy of Mg and antioxidants are important risk factors in predisposing to leukemias.[iv] Other researchers found that 46% of the patients admitted to an ICU in a tertiary cancer center presented hypomagnesemia. They concluded that the incidence of hypomagnesemia in critically ill cancer patients is high.[v] In animal studies we find that Mg deficiency has caused lymphopoietic neoplasms in young rats. A study of rats surviving Mg deficiency sufficient to cause death in convulsions during early infancy in some, and cardiorenal lesions weeks later in others, disclosed that some of survivors had thymic nodules or lymphosarcoma.[vi]

One would not normally think that Magnesium (Mg) deficiency can paradoxically increase the risk of, or protect against cancer yet we will find that just as severe dehydration or asphyxiation can cause death magnesium deficiency can directly lead to cancer. When you consider that over 300 enzymes and ion transport require magnesium and that its role in fatty acid and phospholipids acid metabolism affects permeability and stability of membranes, we can see that magnesium deficiency would lead to physiological decline in cells setting the stage for cancer. Anything that weakens cell physiology will lead to the infections that surround and penetrate tumor tissues. These infections are proving to be an integral part of cancer. Magnesium deficiency poses a direct threat to the health of our cells. Without sufficient amounts our cells calcify and rot in. Breeding grounds for yeast and fungi colonies they become, invaders all to ready to strangle our life force and kill us.

Over 300 different enzymes systems rely upon magnesium to facilitate their catalytic action, including ATP metabolism, creatine-kinase activation, adenylate-cyclase, and sodium-potassium-ATPase.[vii]

It is known that carcinogenesis induces magnesium distribution disturbances, which cause magnesium mobilization through blood cells and magnesium depletion in non-neoplastic tissues. Magnesium deficiency seems to be carcinogenic, and in case of solid tumors, a high level of supplemented magnesium inhibits carcinogenesis.[viii] Both carcinogenesis and magnesium deficiency increase the plasma membrane permeability and fluidity. Scientists have in fact found out that there is much less Mg++ binding to membrane phospholipids of cancer cells, than to normal cell membranes.[ix]

Magnesium protects cells from aluminum, mercury, lead, cadmium, beryllium and nickel.

Magnesium in general is essential for the survival of our cells but takes on further importance in the age of toxicity where our bodies are being bombarded on a daily basis with heavy metals. Glutathione requires magnesium for its synthesis.[x] Glutathione synthetase requires ?-glutamyl cysteine, glycine, ATP, and magnesium ions to form glutathione.[xi] In magnesium deficiency, the enzyme y-glutamyl transpeptidase is lowered.[xii] According to Dr. Russell Blaylock, low magnesium is associated with dramatic increases in free radical generation as well as glutathione depletion and this is vital since glutathione is one of the few antioxidant molecules known to neutralize mercury.[xiii] Without the cleaning and chelating work of glutathione (magnesium) cells begin to decay as cellular filth and heavy metals accumulates; excellent environments to attract deadly infection/cancer.

There is drastic change in ionic flux from the outer and inner cell membranes both in the impaired
membranes of cancer, and in Mg deficiency.

Anghileri et al[xiv],[xv] proposed that modifications of cell membranes are principal triggering factors in cell transformation leading to cancer. Using cells from induced cancers, they found that there is much less magnesium binding to membrane phospholipids of cancer cells, than to normal cell membranes.[xvi] It has been suggested that Mg deficiency may trigger carcinogenesis by increasing membrane permeability.[xvii] Magnesium deficient cells membranes seem to have a smoother surface than normal, and decreased membrane viscosity, analogous to changes in human leukemia cells.[xviii],[xix] There is drastic change in ionic flux from the outer and inner cell membranes (higher Ca and Na; lower Mg and K levels), both in the impaired membranes of cancer, and of Mg deficiency. And we find that lead (Pb) salts, are more leukemogenic when given to Mg deficient rats, than when they are given to Mg-adequate rats, suggesting that Mg is protective.[xx]

Magnesium has an effect on a variety of cell membranes through a process involving calcium channels and ion transport mechanisms. Magnesium is responsible for the maintenance
of the trans-membrane gradients of sodium and potassium.

Long ago researchers postulated that magnesium supplementation of those who are Mg deficient, like chronic alcoholics, might decrease emergence of malignancies[xxi] and now modern researchers have found that all types of alcohol — wine, beer or liquor — add equally to the risk of developing breast cancer in women. The researchers, led by Dr. Arthur Klatsky of the Kaiser Permanente Medical Care Program in Oakland , Calif. , revealed their findings at a meeting of the European Cancer Organization in Barcelona in late 2007. It was found that women who had one or two drinks a day increased their risk of developing breast cancer by 10 percent. Women who had more than three drinks a day raised their risk by 30 percent. The more one drinks the more one drives down magnesium levels.

Breast cancer is the second most common cancer killer of women, after lung cancer. It will be diagnosed in 1.2 million people globally this year and will kill 500,000.

According to data published in the British Journal of Cancer in 2002, 4 percent of all breast cancers — about 44,000 cases a year — in the United Kingdom are due to alcohol consumption. It’s an important question though, and one not asked by medical or health officials, is it the alcohol itself or the resultant drop in magnesium levels that is cancer provoking? Though some studies have shown that light- to moderate alcohol use can protect against heart attacks it does us no good to drink if it cause cancer. Perhaps if magnesium was supplemented in women drinkers who were studied there would have been no increase of cancer from drinking.

Alcohol has always been known to deplete magnesium, and is one of the first supplements given to alcoholics when they stop and attempt to detoxify and withdraw.

Researchers from the School of Public Health at the University of Minnesota have just concluded that diets rich in magnesium reduced the occurrence of colon cancer.[xxii] A previous study from Sweden[xxiii] reported that women with the highest magnesium intake had a 40 per cent lower risk of developing the cancer than those with the lowest intake of the mineral.

Pre-treatment hypomagnesemia has been reported in young leukemic children, 78% of whom have histories of anorexia, and have excessive gut and urinary losses of Mg.[xxiv]

Several studies have shown an increased cancer rate in regions with low magnesium levels in soil and drinking water, and the same for selenium. In Egypt the cancer rate was only about 10% of that in Europe and America . In the rural fellah it was practically non-existent. The main difference was an extremely high magnesium intake of 2.5 to 3g in these cancer-free populations, ten times more than in most western countries.[xxv]

The School of Public Health at the Kaohsiung Medical College in, Taiwan, found that magnesium also exerts a protective effect against gastric cancer, but only for the group with the highest levels.[xxvi]

If we looked it would probably be very difficult to find a cancer patient with anywhere near normal levels of cellular magnesium meaning cancer probably does not exist in a physical cellular environment full of magnesium. It makes perfect medical sense to saturate the body with magnesium through transdermal means. Magnesium deficiency has been implicated in a host of clinical disorders but the medical establishment just cannot get it through its thick skull that it is an important medicine.

It is as if the collective medical profession had just pulled the plug on medical intelligence. In fact it has done exactly this and it seems too late for it to redefine itself, which is a tragedy. Though magnesium improves the internal production of defensive substances, such as antibodies and considerably improves the operational activity of white granulozytic blood cells (shown by Delbert with magnesium chloride), and contributes to many other functions that insure the integrity of cellular metabolism, no one thinks to use it in cancer as a primary treatment. It is even worse than this, the medical establishment does not even use magnesium as a secondary treatment or even use it at all and gladly uses radiation and chemo therapy, both of which force magnesium levels down further.

To not replete cellular magnesium levels would be negligent especially in the case of cancer where a person’s life is on the line. An oncologist who ignores his patient’s magnesium levels would be analogous to an emergency room physician not rushing resuscitation when a person stops breathing. If one elects to have or has already had chemotherapy they have four times the reason to pay attention to a concentrated protocol aimed at replenishing full magnesium cellular stores.

Magnesium chloride is the first and most important item in any person’s cancer treatment strategy. Put in the clearest terms possible, our suggestion from the first day on the Survival Medicine Cancer Protocol is to almost drown oneself in transdermally applied magnesium chloride. It should be the first not the last thing we think of when it comes to cancer. It takes about three to four months to drive up cellular magnesium levels to where they should be when treated intensely transdermally but within days patients will commonly experience its life saving medical/healing effects. For many people whose bodies are starving for magnesium the experience is not too much different than for a person coming out of a desert desperate for water. It is that basic to life, that important, that necessary.

That same power found in magnesium that will save your life in the emergency room during cardiac arrest, that will diminish damage of a stroke if administered in a timely fashion is the same power that can save one’s life if one has cancer. All a patient has to do is pour it into their baths or spray it right onto their bodies. What could be simpler?

Magnesium chloride, when applied directly
to the skin, is transdermally absorbed and has an
almost immediate effect on chronic and acute pain.

Special Note on Calcium and Cancer:

Experts say excessive calcium intake may be unwise in light of recent studies showing that high amounts of the mineral may increase risk of prostate cancer. “There is reasonable evidence to suggest that calcium may play an important role in the development of prostate cancer,” says Dr. Carmen Rodriguez, senior epidemiologist in the epidemiology and surveillance research department of the American Cancer Society (ACS). Rodriguez says that a 1998 Harvard School of Public Health study of 47,781 men found those consuming between 1,500 and 1,999 mg of calcium per day had about double the risk of being diagnosed with metastatic (cancer that has spread to other parts of the body) prostate cancer as those getting 500 mg per day or less. And those taking in 2,000 mg or more had over four times the risk of developing metastatic prostate cancer as those taking in less than 500 mg.

Calcium and magnesium are opposites in their effects
on our body structure. As a general rule, the more
rigid and inflexible our body structure is, the
less calcium and the more magnesium we need.

Later in 1998, Harvard researchers published a study of dairy product intake among 526 men diagnosed with prostate cancer and 536 similar men not diagnosed with the disease. That study found a 50% increase in prostate cancer risk and a near doubling of risk of metastatic prostate cancer among men consuming high amounts of dairy products, likely due, say the researchers, to the high total amount of calcium in such a diet. The most recent Harvard study on the topic, published in October 2001, looked at dairy product intake among 20,885 men and found men consuming the most dairy products had about 32% higher risk of developing prostate cancer than those consuming the least.

The adverse effects of excessive calcium intake may include high blood calcium levels, kidney stone formation and kidney complications.[xxvii] Elevated calcium levels are also associated with arthritic/joint and vascular degeneration, calcification of soft tissue, hypertension and stroke, and increase in VLDL triglycerides, gastrointestinal disturbances, mood and depressive disorders, chronic fatigue, and general mineral imbalances including magnesium, zinc, iron and phosphorus. High calcium levels interfere with Vitamin D and subsequently inhibit the vitamin’s cancer protective effect unless extra amounts of Vitamin D are supplemented.[xxviii]

Magnesium is the mineral of rejuvenation and prevents
the calcification of our organs and tissues that is
characteristic of the old-age related degeneration of our body.

Recommendations of magnesium to calcium ratios range from 1:2 to 1:1. For those interested in preventing cancer one should look closely at the 1:1 camp and during the first six months of treatment one should be looking at ten parts magnesium to one part calcium. In reality one need not even count the ratio during the first months for the only real danger of extremely high magnesium levels comes with patients suffering from kidney failure. If one is at all concerned about their calcium intake one should eat foods high in both calcium and magnesium like toasted sesame seeds.


Up to 30% of the energy of cells is
used to pump calcium out of the cells.

Doctors who have used intravenous magnesium treatments know the benefits of peaking magnesium levels, even if only temporarily. For the cancer patient the transdermal approach combined with oral use offers the opportunity to take magnesium levels up strongly and quickly. For emergency situations three applications a day, for urgent two treatments would be indicated though one strong treatment with an ounce of a natural magnesium chloride solution spread all over the body like a sun screen is a powerful systemic treatment.

Calcium requirement for men and
women is lower than previously estimated.
US Department of Agriculture

It is medical wisdom that tells us that magnesium is actually the key to the body's proper assimilation and use of calcium, as well as other important nutrients. If we consume too much calcium, without sufficient magnesium, the excess calcium is not utilized correctly and may actually become toxic, causing painful conditions in the body. Hypocalcemia is a prominent manifestation of magnesium deficiency in humans (Rude et al., 1976). Even mild degrees of magnesium depletion significantly decreases the serum calcium concentration (Fatemi et al., 1991).

Mark Sircus Ac., OMD
Director International Medical Veritas Association
http://www.imva.info
http://www.magnesiumforlife.com
Sanctuary Cancer Clinic

Product Information: In my clinical work with patients I am using two grades of natural magnesium chloride. The first is the finest in the world coming from a deep underground deposit in Europe that is over 200 million years old. Talking about purity this is what you want to use to put in nebulizers for aerosol treatment, for oral use, eye wash, douches, and for sensitive skin. And for cancer of the skin or breast this is the magnesium chloride to use. Also for doctors who want to use magneisum intravenously this is a much higher grade than anything pharmaseutically sourced. The second is the sea water evaportation magnesium chloride, which is more cost effective for baths and intensive body spraying. Contact Rob Behr from Ancient Minerals in Europe for international sales information and Jared Ramirez from LL Magnetic Clay for the United States and Canada.

[i] Mg2+ is critical for all of the energetics of the cells because it is absolutely required that Mg2+ be bound (chelated) by ATP (adenosine triphosphate), the central high energy compound of the body. ATP without Mg2+ bound cannot create the energy normally used by specific enzymes of the body to make protein, DNA, RNA, transport sodium or potassium or calcium in and out of cells, nor to phosphorylate proteins in response to hormone signals, etc. In fact, ATP without enough Mg2+ is non-functional and leads to cell death. Bound Mg2+ holds the triphosphate in the correct stereochemical position so that it can interact with ATP using enzymes and the Mg2+ also polarizes the phosphate backbone so that the 'backside of the phosphorous' is more positive and susceptible to attack by nucleophilic agents such as hydroxide ion or other negatively charged compounds. Bottom line, Mg2+ at critical concentrations is essential to life,” says Dr. Boyd Haley who asserts strongly that, “All detoxification mechanisms have as the bases of the energy required to remove a toxicant the need for Mg-ATP to drive the process. There is nothing done in the body that does not use energy and without Mg2+ this energy can neither be made nor used.” Detoxification of carcinogenic chemical poisons is essential for people want to avoid the ravages of cancer. The importance of magnesium in cancer prevention should not be underestimated.

[ii] Magnesium has a central regulatory role in the cell cycle including that of affecting transphorylation and DNA synthesis, has been proposed as the controller of cell growth, rather than calcium. It is postulated that Mg++ controls the timing of spindle and chromosome cycles by changes in intracellular concentration during the cell cycle. Magnesium levels fall as cells enlarge until they reach a level that allows for spindle formation. Mg influx then causes spindle breakdown and cell division.

[iii] Hunt, B.J., Belanger, L.F. Localized, multiform, sub-periosteal hyperplasia and generalized osteomyelosclerosis in magnesium-deficient rats. Calcif. Tiss. Res. 1972; 9:17-27.

[iv]Aleksandrowicz, J., Blicharski, J., Dzigowska, A., Lisiewicz, J. Leuko- and oncogenesis in the light of studies on metabolism of magnesium and its turnover in biocenosis. Acta Med. Pol. 1970; 11:289-302. (abstr: Blood 1971; 37:245)

[v] D. Deheinzelin, E.M. Negri1, M.R. Tucci, M.Z. Salem1, V.M. da Cruz1, R.M. Oliveira, I.N. Nishimoto and C. Hoelz. Hypomagnesemia in critically ill cancer patients: a prospective study of predictive factors. Braz J Med Biol Res, December 2000, Volume 33(12) 1443-1448

[vi] Bois, P. Tumour of the thymus in magnesium-deficient rat. Nature 1964; 204:1316.

[vii] Magnesium is used in the creatine-phosphate formation, activates the alkaline phosphatase and pyrophosphatase, stabilizes nucleic acid synthesis, concerning DNA synthesis and degradation, as well as the physical integrity of the DNA helix, activates amino acid and protein synthesis, and regulates numerous hormones.

[viii] Durlach J, Bara M, Guiet-Bara A, Collery P. Relationship between magnesium, cancer and carcinogenic or anticancer metals. Anticancer Res. 1986 Nov-Dec;6(6):1353-61.

[ix]Anghileri, L.J. Magnesium concentration variations during carcinogenesis. Magnesium Bull. 1979; 1:46-48.

[x] Linus Pauling Institute http://lpi.oregonstate.edu/infocenter/minerals/magnesium/index.html#function

[xi] Virginia Minnich, M. B. Smith, M. J. Brauner, and Philip W. Majerus. Glutathione biosynthesis in human erythrocytes. Department of Internal Medicine, Washington University School of Medicine, J Clin Invest. 1971 March; 50(3): 507–513. Abstract: The two enzymes required for de novo glutathione synthesis, glutamyl cysteine synthetase and glutathione synthetase, have been demonstrated in hemolysates of human erythrocytes. Glutamyl cysteine synthetase requires glutamic acid, cysteine, adenosine triphosphate (ATP), and magnesium ions to form ?-glutamyl cysteine. The activity of this enzyme in hemolysates from 25 normal subjects was 0.43±0.04 µmole glutamyl cysteine formed per g hemoglobin per min. Glutathione synthetase requires ?-glutamyl cysteine, glycine, ATP, and magnesium ions to form glutathione. The activity of this enzyme in hemolysates from 25 normal subjects was 0.19±0.03 µmole glutathione formed per g hemoglobin per min. Glutathione synthetase also catalyzes an exchange reaction between glycine and glutathione, but this reaction is not significant under the conditions used for assay of hemolysates. The capacity for erythrocytes to synthesize glutathione exceeds the rate of glutathione turnover by 150-fold, indicating that there is considerable reserve capacity for glutathione synthesis. A patient with erythrocyte glutathione synthetase deficiency has been described. The inability of patients' extracts to synthesize glutathione is corrected by the addition of pure glutathione synthetase, indicating that there is no inhibitor in the patients' erythrocytes.

[xii] Braverman, E.R. (with Pfeiffer, C.C.)(1987). The healing nutrients within: Facts, findings and new research on amino acids. New Canaan : Keats Publishing

[xiii] http://www.dorway.org/blayautism.txt

[xiv] Anghileri, L.J. Magnesium concentration variations during carcinogenesis. Magnesium Bull. 1979; 1:46-48.

[xv] Anghileri, L.J., Collery, P., Coudoux, P., Durlach, J. (Experimental relationships between magnesium and cancer.) Magnesium Bull. 1981; 3:1-5

[xvi] Anghileri, L.J., Heidbreder, M., Weiler, G., Dermietzel, R. Hepatocarcinogenesis by thioacetamide: correlations of histological and biochemical changes, and possible role of cell injury. Exp. Cell. Biol. 1977; 45:34-47.

[xvii] Blondell, J.W. The anticancer effect of magnesium. Medical Hypothesis 1980; 6:863-871.

[xviii] Whitney, R.B., Sutherland, R.M. The influence of calcium, magnesium and cyclic adenosine 3'5'-monophosphate on the mixed lymphocyte reaction. J. Immunol. 1972; 108:1179-1183.

[xix] Petitou, M., Tuy, F., Rosenfeld, C., Mishal, Z., Paintrand, M., Jasmin, C., Mathe, G., Inbar, M. Decreased microviscosity of membrane lipids in leukemic cells; two possible mechanisms. Proc. Natl. Acad. Sci. USA 1978; 75:2306-2310.

[xx] Hass, G.M., McCreary, P.A., Laing, G.H., Galt, R.M. Lymphoproliferative and immumunologic aspects of magnesium deficiency. In Magnesium in Health and Disease (from 2nd Intl Mg Sympos, Montreal , Canada , 1976), b Eds. M. Cantin, M.S. Seelig, Publ. Spectrum Press, NY, 1980, pp 185-200

[xxi] Collery, P., Anghileri, L.J., Coudoux, P., Durlach, J. (Magnesium and cancer: Clinical data.) Magnesium Bull. 1981; 3:11-20.

[xxii] American Journal of Epidemiology (Vol. 163, pp. 232-235)

[xxiii] Journal of the American Medical Association, Vol. 293, pp. 86-89

[xxiv] Paunier, L., Radde, I.C.: Normal and abnormal magnesium metabolism. Bull. of Hosp. for Sick Childr. ( Toronto ) 1965; 14:16-23.

[xxv] MAY 19, 1931, Dr. P. Schrumpf-Pierron presented a paper entitled "On the Cause Of the Rarity of Cancer in Egypt ," which was printed in the Bulletin of the Academy of Medicine, and the Bulletin of the French Association for the Study of Cancer in July, 1931. http://www.mgwater.com/rod02.shtml

[xxvi] Yang CY et al. Jpn J Cancer Res.1998 Feb;89 (2):124-30. Calcium, magnesium, and nitrate in drinking water and gastric cancer mortality.

[xxvii] New York State Department of Health; http://www.health.state.ny.us/diseases/conditions/osteoporosis/qanda.htm

[xxviii] Accu-Cell Nutrition; Calcium and Magnesium http://www.acu-cell.com/acn.html


Dr. Hammer's "The New Medicine"--Broken Souls
Dear IMVA,

The following essay is from HeartHealth, and is one of the 270 chapters in the Survival Medicine compendium (2,200 pages), which we will be publishing next week. Below you will find a rare document of beauty - words of love and comprehension. Putting together the compendium has offered me a stroll down many of the lanes I have traveled in my life that have led me up to the present moment and life's work.

Several people have been mentioning The New Medicine from Dr. Hammer and the below, despite all I write about orthomolecular medicine, shows where I am really am in my soul about health, medicine and treating people in need. Being a doctor of the soul is not an easy job but sometimes that is the level a doctor needs to work to relieve conflicts in their patients lives. Many people have had intentional harm done to them and medicine does not deal well with these harsh realities. Dr. Hammer talks about conflicts and how momumental life shocks can trigger the decline into cancer. Below I talk about something else, about the heart and its grace and the vital healing energy that flows through it when we are open to the vulnerabilities in our hearts and souls.

Mark Sircus Ac., OMD
Director International Medical Veritas Association
http://www.imva.info
http://www.magnesiumforlife.com
Sanctuary Cancer Clinic

Grace of the Heart

Both western medicine and modern psychology have not been able to come up with solid concepts that explain why some people recover from illness and others do not. There does seem to be a force in most everyone that operates routinely to protect and promote health, whose absence seems to leave us vulnerable. This explains, on some level, why one individual might suffer a relatively mild attack of a disease like ulcerative colitis, another gets chronically crippled by the same disease, and a third might decline rapidly from the first attack and go on to die from the same thing another recovers quickly from. Many physicians and therapists have noticed that certain people have a strong will to get better. There are some individuals who can become extremely sick, and because of an exceptionally ‘strong will to grow,’ heal. And there are people who suffer from mild illnesses, who lack this will, and despite the best of treatment and care, languish inside of their illness. They will not show significant improvements, or if they do, will end up bouncing from one illness to another.

Our will is what the heart wants to do.

Dr. Christopher Hills

Whatever our heart loves it has the will for. This connection between heart and will offers us a clue to the `secret` forces at work in our ability to resist disease or recover from illness quickly. The heart is at the center of more than we can dream of yet it is a factor that is not at all understood or even recognized by contemporary psychiatric or medical theory. Simply put, it is the abandonment of the seat of feelings, the repression and denial of the heart that is at the center of much illness and disease. The displacement effect of the heart, driven to the bottom of human consciousness, is terrible to behold and more terrible to experience. When we repress our heart felt feelings we repress our beings and this is something impossible to do without paying a steep price in terms of mental, emotional and physical health.

The heart center is where we experience our being.

The distance we travel away from our own heart
and true being is the same distance we travel
away from the happiness of our health.

Psychosomatic is the global term used by many doctors and psychologists to refer to causes beyond the purely physical, beyond genetic accidents and beyond things like AIDS or being hit by a truck. That the psyche is somehow involved in the causation of various illnesses and the general collapse or weakening of the immune system is known. Yet doctors do not have the training or understanding to make this knowledge useful to their patients. To tell someone it’s all in your head does not help. The knowledge that individuals with certain personality patterns have lower resistances and higher incidences of certain diseases does not translate into a workable system that aids us on the practical level of diagnosis and treatment of mental, emotional or physical disease.

It might take time for modern science, medicine, and psychology to understand and believe it, but the heart is at the center of much of the mysteries that have confounded rational thinkers for millenniums. When we say that the heart is the vulnerability of being we are making a direct connection between what we are calling the heart and our pure being. Pure heart or pure being is very different from the space of the thinking mind. One thinks, the other feels. Though in consciousness both mind and being co-exist, one is more fundamental to life then the other. Mind based personality patterns in and of themselves are not at the root of disease directly. What is both important is the effect each and every person’s personality (thoughts) have on the heart. Egocentric patterns do their damage by ripping us away from the heart. They tear our connection with our own inner being. The evil of personality is seen only in how it separates us from the heart and universe of true being (feelings).

Grace is the flow of pure heart energy.

It heals, enlightens and warms us.

It touches us where we need to be touched.

There is a quality of heart and pure being that can be called grace. The grace of the heart offers us a quality of being that is healing, animating, invigorating, supporting, nurturing, and comforting. The grace of the heart offers an inner tranquility and peace that the mind by itself rarely possesses. The essence of the heart is love, light and health. It represents our being nature and that nature is given to us by the cosmic intelligence with these highly positive qualities. Yet it does seem that some people’s hearts are so small that they seem not to exist at all. Somehow man through his society, religion, law and politics has found a way to almost completely squash the universe of heart, love, being and soul.

The Intelligence, Love and Power of the heart acts

routinely to protect and to foster health on all levels.

It is this intelligence and protecting love force that
guides our steps and makes all the difference in life.

It is this power that charms our life.

Deep in the nuclear core of the heart is a love of life and a love of love. Some beings come here to earth with such a strong heart that no circumstance can beat it out of them. In them is a furnace of heart energy and like the sun it will not be denied though they might have to go through great struggles to release and express this energy. Though we all have hearts, the problem with life comes with the repression of the light and radiance of the heart. What we are born with hardly remains by the time we reach adulthood. And the path of regaining what was lost is a path of lifelong learning, growth, and often-painful experience.

The pure heart stops all thinking, all imagining
and just experiences things and people as they are.

Mental, emotional and even physical illness occurs because our conscious mind resists the normally more unconscious wisdom of the heart. Scott Peck said “mental illness occurs when the conscious will of the individual deviates substantially from the will of God, which is the individuals own unconscious will.” The will of God can be seen in the basic structure of consciousness that is hard wired into our beings. This is the love of love, love of life and the capacity to feel this love, and feel when this love is being hurt.

The heart is the only thing strong enough
to cut through the illusions of the mind.
Consciousness is stronger than mind stuff,
and the experience of pure consciousness is found
when we step through the portal of the open and pure heart.

So the real heart of this book, its real message is to put all of your attention on the heart, to tack against the strong winds of the mental world of thought, which even when diminished will still strongly occupy the seat of consciousness, and cave dive into the essence of true intelligence, the intelligence and healing power of the heart. The heart offers us a grace, a power and a will toward what is right and what is certain for our existence.

Though HeartHealth talks about the pure heart, and achieving the experience of it is thought to be a worthy goal, we are hardly advocating a total abandonment of the conscious rational or conceptual mind functions. Though these conscious mental functions might need to be put in their proper place in consciousness they are essential aspects of our being also.

The pure heart has no sense of self-image.

The pure heart is no longer thinking about itself

and is beyond all levels of imagination.

Our heart just is and just feels.

It cares and feels itself to be part of the whole.

Part of the Oneness of Being.
It is in the oneness that the true heart appears.

The real pure heart does not have to be controlled from without. It does not need religious codes of behavior. Each individual heart, which is not really divisible from the whole, shines with a light of great intelligence. The pure heart feels, understands what it feels, gathers the full wisdom and intelligence from those feelings, and then responds, moves, and changes life directions. The pure heart does this equally well when listening to its own feelings or the feelings of another. When we can listen to our husbands and wives this way, and then our children this way, we will have begun the creation of heaven on earth. Now that we have almost destroyed the family, the basic social unit of life The Marriage of Souls lays down a new blueprint for the resurrection of family and social life.

Our pure beings need pure love, deserve pure love,

live on pure love. The Marriage of Souls is about

pure beings "sharing" pure love. The pure light of pure being,

perfectly vulnerable, perfectly feeling, perfectly real.


Nascent Iodine
Nascent Iodine

Iodine is utilized by every hormone receptor in the body.
The absence of iodine causes a hormonal dysfunction that
can be seen with practically every hormone inside the body.

Nascent Iodine is a scientific term for iodine where the iodine molecule has the diatomic bond broken and has a high amount of electromagnetic energy associated with it. During the 2 to 3 hour of activation time (within the human body, once diluted in water and consumed) the nascent iodine atom has the ability to be of assistance to the body. This form of iodine is produced by subjection of a 1 % tincture of iodine to a high electro magnetic field for a given time in order to produce the nascent iodine state. This atomic state and electromagnetic charge is held by the atom until diluted in water and consumed. Once diluted and inside the body this atom is readily absorbed and utilized by the body. This charged atom of iodine starts a process where it gradually loses its energy over 2 to 3 hours. During this time the body recognizes this atom as the same nascent iodine it produces in the thyroid in order to make the T3 and T4 hormones.

The atomic iodine is perhaps the least toxic and
least irritating of all the iodine formulas available.

The quality that separates nascent iodine from all other iodine products is that the diatomic bond is broken with each atom keeping one of the two electrons that had made up the covalent bond. This is known as homolytic cleavage and causes the iodine atom to be subject to magnetic charging. The iodine being in the atomic state was the reason it was called Atomidine, for Atomic Iodine (1926 to 1935). This atomic state and large electromagnetic charge is held by the atom until diluted in water where it then rapidly looses its charge.

Nascent Iodine is a complete atom
no extra electrons none missing.

It was the famous psychic Edgar Cayce, who suggested iodine for all sorts of thyroid problems, who advised that it would be necessary to electrically charge the iodine to change it into its "atomic" form. This charging converts the iodine into a form that the body can most fully recognize and assimilate. (Iodine trichlorite claims to be atomic iodine, but it’s not.) A true atomic iodine is the best kind to bring the thyroid to its optimal function because it supports and saturates the thyroid without any toxic buildup.

Iodine is a well known topical germicidal agent effective against a wide spectrum of organisms including bacteria, fungi and protozoa. Iodine is normally available as solutions, alcoholic tinctures and iodophors. Iodophors were developed because iodine tinctures caused skin irritation, severe hypersensitivity reactions and systemic absorption of iodine. Iodophors are compounds of iodine linked to carriers for iodine and only a small amount of iodine is released minimizing toxicity, which is not really a problem at all when iodine is administered in its pure atomic form.

Iodine has bactericidal activity, e.g. a 1% tincture
will kill 90% of bacteria in 90 seconds, a 5% tincture
in 60 seconds and a 7% tincture in 15 seconds.

Gershenfeld, 1968

Iodide uptake by the thyroid is an active process.[i] So much of the information on iodine insists that iodine should be taken in its two major forms, iodide and iodine. An iodide ion is an iodine atom with a -1 charge. Compounds with iodine in formal oxidation state -1 are called iodides. Dr. David Brownstein wrote that “it is very difficult to get iodine into a solution that uses water as a solvent. Therefore as Dr. Lugol discovered, using the reduced form of iodine (iodide) increases the solubility of iodine.” Atomic or Nascent Iodine is not dissolved in water but in alcohol.

I have used various iodide preparations
for years with mixed success.
Dr. David Brownstein

Iodized salt and the iodine supplements usually found in health food stores contain the iodide form of iodine but Dr. Brownstein, one of the world’s iodine experts has had little success treating patients with only iodide. The supplement Iodoral contains both the iodide (reduced) and iodine (oxidized) forms of iodine. The US RDA for iodine is 150 mcg. Iodoral contains 100 times (12.5 mgs) the RDAs requirement of iodine/iodide. One drop of Nascent iodine = RDA of 0.2 mg. If using for additional energy and general improved health take up to 5 drops daily. That would mean only one milligram.

We do in fact find that when taking a nascent form of iodine, therapeutic doses are much lower. If recommended by your healthcare professional for assistance with a chronic health concern take 5 drops three or four times a day or as instructed by your healthcare professional. Thirty drops per day is the equivalent of 6 mg. of iodine or 1 drop of Lugol's iodine. Frequent small doses are more effective than larger amounts at less frequent intervals. Always take on an empty stomach. Most will find that it is important to build up gradually in order to experience the least amount of detoxification reaction. (See chapter Iodine and Chelation) It is best when using strong chelators, which iodine is, to moderate the amount of detoxification symptoms or what is called the Herxemeirs reaction, which is the experience of poisons being dumped into the blood stream from the cells or from large scale yeast die offs. This is most readily controlled with iodine in the atomic form simply because it is so easy to control and regulate the dose.

Iodine is an easily oxidisable substance. Food that is present in the digestive tract will oxidize iodine to iodide which is not corrosive to the gastrointestinal tract. Oral iodine appears to be inactivated by combination with gastrointestinal contents. Absorption is poor due to rapid conversion of iodine to iodide[ii] and this might explain why one needs to take very high doses of Iodoral or Lugols compared to nascent iodine, which seems to bypass the digestive track altogether meaning its absorption starts right in the mouth and continues through direct penetration of the stomach tissues. The nascent appears to go into direct use by the body directly as soon as it is exposed to soft tissues. This is no stretch of the imagination since we know that iodide is completely and rapidly absorbed throughout all areas of the GI tract. Dr. Brownstein says that the downside of Lugol’s solution is the taste and the dosing of it. Lugol’s has a distinct metallic taste that many people find offensive. The atomic iodine on the other hand is like sipping on a heavenly gift, you can sense in a millisecond its positive nature.

Iodide has to be converted back to the nascent form in order to produce T3 and T4. Would the body not recognize nascent iodine as what is needed in the thyroid and take it there to avoid the steps of active transport to produce nascent iodine when it already has it available? This could explain why some people report that they feel the atomic form of iodine in their thyroid within 10 minutes. Is there really time for the iodine to get into the intestines and be converted into an iodide to be shipped to the thyroid?

Sunkar A. Bisey a Hindu scientist was suffering from malaria in the early nineteen-hundreds and quinine didn't do him any good. His life was despaired of, and a Hindu doctor, hoping to save the life of India 's greatest inventor, sent on a few doses of a Burmese preparation, made from seaweed, that had proved useful in treating chronic malaria there. Bisey tried it. The effect was electrical. He began to improve at once and in a month was a well man. He set out to research the contents of the seaweed and ended up producing the compound now known as Beslin or atomic iodine. Atomic iodine is iodine molecules broken down to individual atoms, which is the exact form that the body needs to make thyroid hormones. If iodine is not in the atomic form the molecules of iodine first need to be broken down and that of course takes energy.

Malaria was treated with 20 drops of nascent iodine in a half glass of water given 4 or 5 times during the first day and then going to 10 drops of nascent iodine 4 times a day for 3 more days. A slide study of the blood shows that the malaria is gone from the body. It is interesting to note that Salem Banajeh, Associate Professor-Child Health at Sana'a University-Sana'a-Yemen found that case fatality for malaria is 4 times higher in highlands compared with endemic areas.[iii] Iodine deficiency would explain this, which would explain why iodine is an effective treatment for malaria.

Dr. A. Regnault, while recognizing the great value of quinine in the treatment of malaria, said in 1901 that it was becoming a matter of general recognition that the quinine-series of drugs is of service only during certain developmental periods of the disease. It is held that the toxins are developed with great rapidity just at the time of the division of the parasites. In order to eliminate these toxins, Dr. Regnault suggested the use of iodine and potassium iodide, iodine being a body which has a special affinity for bodies of the alkaloid class, and presumably for the supposed analogies of these toxins. The results obtained were reported as being very striking in that not only were the attacks aborted, but the action on the fever itself was striking and immediate with chills, vomiting and malaise disappearing rapidly. The remedies were employed in the following strength: Tincture of Iodine and potassium iodide, of each, 1; distilled water, 25.[iv]

“Iodine has many positive therapeutic actions. It is a potent anti-infective agent. No virus, bacteria or parasite has been shown to be resistant to iodine therapy,” writes Dr. Brownstein. This is an incredible statement but one that can easily be backed by hardcore medical science. It is the reason hospitals use iodine by the gallon and in reality the only reason hospitals are not like ground zero sites contaminated in an infectious sense is because of iodine's broad spectrum anti-infective power.

Few are the doctors who have realized that iodine can be taken internally in large quantities and that it will have the same effect internally as it does on external surfaces. When we look at the fact that the entire focus of vaccines is anti-viral, that bacterial infections are becoming more threatening and more antibiotic resistant, that cancer is always accompanied by and or is a fungal yeast infection, we might begin to realize how iodine can again become a doctor’s best friend. Oncologist Dr. Tullio Simoncini in Rome already uses it for skin and breast cancer but even he has overlooked its potential for internal application for the same action against cancer yeasts and fungi. The secret to successful application in high enough quantities is provided by Nascent Iodine.

Nascent Iodine is more potent in its action because of its
formulation, and because the toxicity has been removed.


When the thyroid becomes fully saturated from continued ingestion of detoxified iodine, whatever it doesn’t need is eagerly grabbed by other tissues of the body independent of the form meaning iodide is not necessary. After the atomic iodine has made its rounds, whatever then remains and is unable to be used is excreted in the urine. The urine will turn bright yellow from the excess, similar to what happens with water-soluble B-vitamins that the body doesn’t need. And, any excess can help the kidneys if there's an infection at the site.

Note: even nascent iodine is safe to use, too much taken too late in the day can be stimulating enough to keep you awake. As with any other supplement, use discretion.

There is a difference between Nascent Iodine and Detoxified Iodine, which itself is a high quality form of iodine. Detoxified Iodine is produced at 10 amps of resistance for five minutes. Nascent Iodine is more difficult to produce. The time required to get iodine into the nascent state is 15 to 20 minutes at 30 amps with a very limited quantity of iodine. The result is that heat is generated and that must be dissipated in order to have the process continue. Historians who have speculated as to why this process was never used in the 1930's by Sunkar A. Bisey to improve his product was that it is just to time consuming and costly to make the nascent iodine through this method. For those who notice the results of nascent iodine it may seem costly to make but well worth it for the results. (I have had several people who have used different iodine products of these types conclusively claim they can feel the difference immediately when taking a true Nascent iodine.)

To quote the 1930's document by Schieffelin and Company:

"The lethal dose of Atomidine (1926 to 1935) in animals is very large, which accounts for the absence of untoward effects in clinical use. Due probably to its rapid absorption and its ready combination with organic compounds in the body, iodism very rarely occurs even in sensitive persons."

If the body does recognize both these qualities, it can then use this charged atom in the thyroid or elsewhere in the body as needed.

The body utilizes more or less nascent iodine depending on the task being addressed. To boost the body systems may require very small amounts, a few drops once a day. The average dose is 5 to 10 drops in one-half glassful of cold water, repeated every two or three hours. Frequent small doses are more effective than larger amounts at less frequent intervals. When an intensive effect is desired 20 or more drops may be administered over the critical period and repeated as required.


Testimonials:

It's 4:30 Thursday, 7-5-07, and I took four drops of Magnascent in water about a half hour ago. As I sit here I can actually FEEL my thyroid gland doing *something* for the third time in about a week, each time after taking at least 4 drops in water on an empty stomach. It feels almost like it is moving in my throat. Well I suppose if it is making hormones and injecting them into my body, a certain amount of movement is to be expected.

For years I have been fighting degenerative arthritis. I have had many successes already with many substances and methods. One thing that has eluded me is a regular, everyday good feeling, and regualr everyday flexibility. I have had many good days in the past few years but always they faltered and I was always searching for some way to keep it up. Now I think I have found it. For about 4 weeks now, starting with taking Detoxified Iodine, but then moving on to Magnascent, I have kept up a level of energy and flexibility that I mostly have not had since I was
about 38 or so (I'm 53).


I get up in the morning and within a short time I'm running through the house ready to get work done, then I'm running through my business shop and yard. At the end of every day I am solidly physically tired, but just get up and go at it all the same way again every day.


The flexibility is just unbelievable. I find myself jumping in and out of trucks and crawling under equipment and working on things while squatting or kneeling with nearly no discomfort. Squatting and kneeling were very uncomfortable for me only a few weeks ago. I used to wince at the thought of having to squat or kneel.


All of this has happened to me on only about 10-12 drops of Magnascent per day. I'm drinking about 8- 10 a day and putting about 2-4 drops a day on a couple of Heberden's Nodes on my hands. Since the endocrine system is all stimulated by iodine and the thyroid, my testosterone is up too. I don't need a test to tell that.


Bob Ansley

A case of Richard D. Norton Jr. with oral cancer had four operations found yet another tumor growing that he could see with a flash light and mirror. He used the nascent iodine for one week three times a day holding it in his mouth a few minutes and then swallowing. In a week he called to ask if the iodine colors skin. I said it was only temporary and then goes back to normal color. He said that he had lost where the cancer was. He couldn't find it. The next week Dr. Anderson his physician confirmed it was gone but they found another in a different location which he is treating it now.

The toxicity of modern life is impacting iodine levels. It is well known that the toxic halides, fluoride and bromide, having structure similar to iodine, can competitively inhibit iodine absorption and binding in the body. Americans, who are more exposed to fluoride than other populations have a desperate need for more iodine and taking iodine in its nascent form would be the best way of increasing iodine levels in the safest and most effective way possible.

In treating over 4,000 patients, Dr. Brownstein has found only three patients with “allergy” to non-radioactive inorganic iodine/ iodide. The nascent form is even less provoking meaning the chances of side effects besides a normal detoxification and chelation response would be near zero. The use of nascent iodine is simple, safe and has proven itself effective through more than a century of medical use. One should turn a deaf ear to all those cynics who would recommend pharmaceutical poisons in its place. They are not unlike the child molester using sweet words to draw an innocent into a deadly web of pain and deceit.

From its position at the base of the brain, the pituitary gland monitors the levels of hormones in the blood. If a low level of thyroid hormones is detected, the pituitary gland sends out its own hormone called thyroid stimulating hormone or TSH, which stimulates the thyroid gland to step up production of thyroid hormones. The thyroid gland can't do this since it's missing one essential ingredient - iodine - but the pituitary gland does not know this. It keeps secreting TSH which after a time will cause the tissue of the thyroid gland to change and the entire gland will enlarge.

Iodine levels have fallen 50% over the last 30 years in the United States . We have also seen at the same time a dramatic drop off of magnesium cellular levels and the same can be said for other minerals like zinc and selenium. During this same time, there have been dramatic increases in illnesses of the breast (including breast cancer), prostate, thyroid and the immune system (i.e., autoimmune disorders). All of these conditions can be caused (in part or wholly) from iodine deficiency as well as magnesium, selenium and zinc deficiencies. Mineral levels should be evaluated in all suffering from illness and those trying to achieve their optimal health. In reality we do not need to expand fortunes in sophisticated testing because unless one is eating a perfect organic whole food diet the chances of being ill and not being mineral deficient is about zero.

Special Note: There is a great deal of confusion by these terms: detoxified iodine, atomic iodine, nascent iodine. Edgar Cayce actually gave out instructions for two different types of iodine, one which is fairly easy to make, or what is called the detoxified form, and the full atomic form or what we are calling Nascent Iodine, which in the opinion of the IMVA, is clearly more potent. Several people who have used one form literally feel the difference at the moment of injection. The only company[v] we are trusting to provide a true Nascent Iodine happens to also be the only company that has applied for a license to supply both the one percent solution, which has been the type of iodine discussed in this chapter, and also a seven percent solution of Nascent Iodine, which now has to be licensed through the drug enforcement (DEA) agency of the government. This type is not for oral use but is perfect for transdermal application, which will be reviewed in another chapter on Transdermal Iodine. This is important to note and have in ones medicine cabinet or dispensary because it is the solution to many diseases of the skin including skin cancer and is a vital part of any protocol for breast cancer as well.

Second Special Note: There has been a lot of commotion in health circles about a product called Miracle Mineral Supplement (MMS). It is being advertised as the answer to AIDS, hepatitis A, B and C, malaria, herpes, TB, most cancer and many more of mankind's worst diseases. The claim about how the chlorine (a poison, not what would be considered a mineral for health)[vi] interacts with pathogens is the same claim we can make about iodine (a safe nutritional mineral), which is known to also kill pathogens of all types on contact. I do not mean to make a qualified medical opinion on MMS, which is chlorine dioxide. Chlorine dioxide is formed from the chemical combination of sodium chlorite and the acetic acid (vinegar) or citric acid. Chlorine dioxide is dangerous to handle and use. A search for material safety data sheets sustains the risk of using this substance.

Chlorine dioxide: May decompose explosively on shock, friction or concussion, or on heating rapidly. Strong oxidant - reacts violently with combustible and reducing materials, and with mercury, ammonia, sulphur and many organic compounds.[vii]

A strong irritant of the skin, eyes, and respiratory tract; [HSDB] A strong oxidizer that promotes combustion; Concentrated solutions may be corrosive to the skin and eyes; Mild hemolytic anemia and increased methemoglobin in males is observed in animal feeding studies; [CHEMINFO][viii]

Acute Health Effects:[ix]

Ingestion: Not a normal route of exposure. Harmful if swallowed. Can cause irritation to mouth,

esophagus, stomach, and mucous membranes.

Eye Contact: Contact causes redness, irritation, pain, blurred vision, tearing, corneal injury and burns.

Inhalation: Harmful if inhaled. Coughing, headaches, labored breathing, nausea, shortness of breath,

pulmonary edema.

Chronic Health Effects:

May have effects on lungs, resulting in chronic bronchitis and permanent lung damage (with chronic exposure).

The use of dangerous poisons is common in allopathic medicine. Even when pharmaceutical companies jump through hoops costing many millions of dollars to test such poisons (most pharmaceuticals are mitochondria poisons) it does not remove the dangers of the poisons, which create all kinds of complications and side effects. The natural allopathic medicine of Survival Medicine only uses such poisons as a last resort.

It almost never makes sense medically to ignore the basics, the air we breathe, the water we drink and the sun. Minerals like magnesium and iodine are up there with the prime basics of life and the use of poisons like chlorine dioxide should not be considered for use unless the basics do not supply the necessary resolution. In the special case of the supposedly magical mineral substance we have something vastly safer, more natural and proven through over a century of medical use. We have iodine, which has the same anti pathogenic profile as that claimed for the chlorine compound.

It is hard to believe that chlorine would
be selective in what it damages or kills.

A later meta-analysis found chlorinated water is associated each year in America with about 4,200 cases of bladder cancer and 6,500 cases of rectal cancer. Chlorine is estimated to account for nine percent of bladder cancer cases and 18 percent of rectal cancers. Those cancers develop because the bladder and rectum store waste products for periods of time. (Keeping the bowels moving regularly lowers such risk.) Chlorinated water is associated with higher total risk of all cancers.[x]

Lastly, the marketing materials and promotion of this chlorine compound are not anchored in medical science or reason. It is very hard to verify claims or trust those who whip up medical hysteria because we never know when testimonials are just projections of the hysteria. The placebo effect is alive and well and its waters fertilized when unsubstantiated claims are made. It makes sense sometime in medicine to take risks but not before medical basics is employed first. Why promote the use of something that has inherent dangers when we have something proven and safe.

Mark Sircus Ac., OMD
Director International Medical Veritas Association
http://www.imva.info
http://www.magnesiumforlife.com
Sanctuary Cancer Clinic

[i] Am J Physiol Endocrinol Metab 273: E1121-E1126, 1997;

Vol. 273, Issue 6, E1121-E1126, December 1997

[ii] Reynolds, 1989; Gosselin et al., 1984, Gilman et al., 1990.

[iii] Abdullah Al-Taiar, Shabbar Jaffar, Ali Assabri, Molham Al-Habori, Ahmed Azazy, Nagiba Al-Mahdi, Khaled Ameen, Brian M Greenwood, and Christopher J M Whitty Severe malaria in children in Yemen: two site observational study BMJ 2006; 333: 827

[iv] Revue de Medicine, 1901, vol xxi., p. 804.

[v] John Brookshire
1316 Shirley way,
Bedford Texas 76022
Phone 817-868-1400
john@magnascent.com
johnb124c@yahoo.com
http://www.magnascent.com/

[vi] Chlorine in swimming pools reacts with organic matter such as sweat, urine, blood, feces, and mucus and skin cells to form more chloramines. Chloroform risk can be 70 to 240 times higher in the air over indoor pools than over outdoor pools.22 Canadian researchers found that after an hour of swimming in a chlorinated pool, chloroform concentrations in the swimmers’ blood ranged from 100 to 1,093 ppb.23 If the pool smells very much of chlorine, don’t go near it.

[vii] http://physchem.ox.ac.uk/MSDS/CH/chlorine_dioxide.html

[viii] http://hazmap.nlm.nih.gov/cgi-bin/hazmap_generic?tbl=TblAgents&id=1559

[ix] http://www.haloxtech.com/pdf/MSDS-Chlorinedioxide(ClO2)-540ppm.pdf

[x] http://www.orthomolecular.org/library/jom/2000/articles/2000-v15n02-p089.shtml


Selenium
Dear IMVA,

Today’s chapter is on item number four in my cancer protocol, selenium. Yes we do have to prioritize things in medicine as we do in life. It escapes people that what we make important in life shapes our life, and it is no different in medicine. After the sun, air and water, magnesium chloride is the number one item in my protocol, iodine is number two, Alpha Lipoic Acid (ALA) number three, selenium is four and after that it’s the sodium bicarbonate.

Bicarbonate is effective in dissolving cancer tumors if it can be applied in a way that gets it close or right up to the tumor. Using sodium bicarbonate is like using a fire extinguisher; it can be sprayed on cancer tumors, which will quickly dissolve if hit right in the face with the bicarbonate. It is number five only because it does not treat the underlying cause or prevent cancer from returning but it does give a great respite to the immune system, which is given enormous help with the elimination of hostile cancer colonies.

We tend to forget the most important items in medicine which are the air we breathe, the water we drink and the sun, which everyone is warning us to stay out of. With the governments in the western hemisphere officially attached to poisoning public water supplies with fluoride, and with air pollution seriously getting out of hand in the northern half of our planet, we are in trouble with our health and doctors are stuck fighting a losing battle against chronic diseases stemming from the massive poisoning of humanity. We do not need to feel compassion for main stream orthodox doctors and dentists though for they have themselves supported the massive use of poisons like mercury.

This chapter from Survival Medicine looms up in importance for the very specific reason that our world is choking on a rising tide of mercury pollution made much worse because of the insane use of mercury in dentistry and medicine. The Rising Tide of Mercury section explains these issues across three hundred and fifty pages of words, words that speak of an invisibly occurring doom happening on the parts per million level. When we take things down to the parts per million and trillion level we witness incredible hurricanes of toxicity and this is what doctors who care about people can no longer ignore.

Mark Sircus Ac., OMD
Director International Medical Veritas Association
http://www.imva.info
http://www.magnesiumforlife.com
Sanctuary Cancer Clinic

PS. Survival Medicine is being uploaded into the e-book format and hopefully the process will be finished by Sunday making it available next Monday if all goes right. Until then it is still available at the pre-publication price of 125 dollars. Approximate length is 2,200 pages. For more information contact luciana@imva.info or go directly to: http://www.imva.info/books.shtml and order.

Selenium, Cancer and Mercury

Selenium, is a reddish-brown solid Metalloid, somewhat
translucent, and of dull metallic glance, insoluble in water,
and alcohol. It exists crystalline, and vitreous; at water's boiling
heat it melts and boils, evolving odour like stale horse-radish.

J. Carrington Sellars, Chemistianity, 1873

Selenium is a potent immune stimulator – the most potent immune stimulator of all some think. Selenium is an essential component of thyroid metabolism and antioxidant defense, as well as immune function. It may improve activation and proliferation of B- lymphocytes and enhance T-cell function.[i] Selenium is essential for our immune system to function at optimal performance. Thus we should not be surprised to find out those cancer patients with low selenium levels tend to have a wider spread of the disease, more recurrences and die sooner. [ii]

Blood selenium levels often indicate the presence
of cancer and even the severity of cancer in a patient.

Selenium influences both the innate, "nonadaptive" and the acquired, "adaptive" immune systems[iii]-[iv]-[v]-[vi]-[vii] The innate immune system includes barriers to infection and nonspecific effector cells such as macrophages. Both the T and B lymphocytes form the major effector cells of the acquired system that mature with exposure to immune challenges. Selenium-deficient lymphocytes are less able to proliferate in response to mitogen, and in macrophages, leukotriene B4 synthesis, which is essential for neutrophil chemotaxis, is impaired by this deficiency. These processes can be improved by selenium supplementation. The humoral system is also affected by selenium deficiency; for example, IgM, IgG and IgA titers are decreased in rats, and IgG and IgM titers are decreased in humans. In endothelial cells from asthmatics, there is a marked selenium deficiency that results in an increase in expression of adhesion molecules, which causes greater adhesion of neutrophils.[viii]

Selenium is also involved in several key metabolic activities through its selenoprotein enzymes that protect against oxidative damage.[ix] Further, selenium deficiency may allow invading viruses to mutate and cause longer-lasting, more severe illness.[x] Animal research has shown selenium and vitamin E have synergistic effects, enhancing the body’s response to bacterial[xi] and parasitic infections.[xii]

Proving the point that selenium is a potent immune stimulator is a 18-month study of 262 patients with AIDS found those who took a daily capsule containing 200 micrograms of selenium ended up with lower levels of the AIDS virus and more health-giving CD4 immune system cells in their bloodstreams than those taking a dummy pill. These AIDS patients who took selenium were able to suppress the deadly virus in their bodies and boost their fragile immune systems, adding to evidence that selenium has healing powers we need to pay attention to in treating cancer patients.[xiii] Those with severely compromised immune systems due to AIDS had dramatically better immune system response with selenium supplementation and this finding is consistent with the information presented by the NIH on their selenium web site.

Selenium is an important weapon against cancer.

As an antioxidant nutrient, selenium prevents the action of free radicals which are believed to be causative agents behind degenerative diseases such as premature ageing, cancer and atherosclerosis.[xiv] Clinical trials have also indicated that selenium can have a role to play in combating oxidative diseases[xv], enhancing the immune response[xvi], increasing male fertility[xvii], improving psychological mood scores[xviii] and reducing the pain and stiffness in arthritis sufferers.[xix]

The implicit importance of selenium to human health is
recognised universally. Selenium is incorporated as
selenocysteine at the active site of a wide range of selenoproteins.

Dr. Emanuel Revici, a Romanian-born physician, scientist, author, and humanitarian[xx] had five major papers on lipids, pain, and cancer deposited by the Pasteur Institute into the eminent National Academy of Sciences during the Second World War. By 1948, Revici had begun exploring the use of selenium in treating cancer and as a means for rendering radiation less harmful. Dr. Revici's use of selenium in the treatment of cancer predates mainstream interest in this mineral by more than twenty years. Selenium is one of the major trace elements always found deficient in cancer-prone populations. Research has shown that it is of value not only in preventing cancer but also in treating it.[xxi]

Revici uses a special molecular form of selenium (bivalent-negative selenium) incorporated in a molecule of fatty acid. In this form, he can administer up to 1 gram of selenium per day, which corresponds to 1 million micrograms per day, reportedly with no toxic side effects. In contrast, too much selenite (hexavalent-positive selenium) has toxic effects on animals, so human intake of commercial selenite is limited to a dosage of only 100 to 150 micrograms by mouth. Dr. Revici often administered his nontoxic form of selenium by injection, usually considered to be four times more powerful than the form given orally.

Dr. Gerhard Schrauzer, professor of biochemistry at the University of California at La Jolla , publicly credited Revici for “having discovered pharmacologically active selenium compounds.” Dr. Gerhard Schrauzer noted almost 30 years ago if every woman in America took 200 micrograms of supplementary selenium daily that breast cancer rates would rapidly decline in the space of a few short years. Dr. Schrauzer is professor emeritus from the University of California , San Diego School of Medicine and has chaired two world conferences on selenium and cancer.

Dr. Richard Donaldson of the St. Louis Veterans' Administration Hospital conducted a clinical trial with terminally ill cancer patients. He found that when he could raise the patients' blood levels of selenium into the normal range, their pain and tumor sizes were often reduced. In a 140 patient study of cancer victims treated with selenium, Dr. Donaldson reported in 1983 that some patients deemed terminal with only weeks to live were completely free of all signs of cancer after four years; all the patients showed a reduction in tumor size and in pain.[xxii]

The amount of selenium needed to obtain normal blood levels varied from person to person. Normal healthy people usually were seen to have normal blood selenium levels on normal diets however it seemed that cancer patients had lower selenium levels on similar diets. (As we will see below this could in great part be due to more intense mercury toxicity in cancer patients.) Apparently they could not get enough without supplements. Dr. Donaldson found that he had to supplement the cancer patients with at least 200 to 600 micrograms of selenium per day and in some cases 2,000 micrograms of selenium per day were required to obtain normal blood selenium levels.

There are now seven population studies in the past six years
that examined the possible connection between selenium and
prostate cancer. All but one of them has found selenium protective.
Karen Collins, R.D.

In one recent study, men with the highest levels of selenium in their blood were about half as likely to develop advanced prostate cancer as the men with the lowest blood selenium. The "Nutritional Prevention of Cancer Project" (NPC) was a controlled, randomized cancer prevention trial in which 1,312 patients received a daily 200 mcg dose of selenium or a placebo for up to 10 years.[xxiii]

A 1996 study by Dr. Larry Clark of the University of Arizona showed just how effective selenium can be in protecting against cancer. In the study of 1,300 older people, the occurrence of cancer among those who took 200 micrograms of selenium daily for about seven years was reduced by 42 percent compared to those given a placebo. Cancer deaths for those taking the selenium were cut almost in half, according to the study that was published in the Journal of the American Medical Association on December 25, 1996. In addition, the people who had taken selenium had 63 percent fewer prostate cancers, 58 percent fewer colorectal cancers, 46 percent fewer lung cancers and overall 37% fewer cancers. Selenium was found to reduce the risk of lung cancer to a greater degree than stopping smoking.[xxiv]

It is noteworthy, that the Food and Drug Administration has determined that there is sufficient evidence to warrant a qualified health claim for Se and cancer. Furthermore, the recent discovery that defects in the SECIS-binding protein 2 (SBP2), which is an indispensable protein for the incorporation of Se into the selenoproteins, result in thyroid dysfunction.[xxv]

Much of what selenium does you can’t feel while it is doing it, but if
you don’t have it, then you will feel it later and you won’t like the
feeling at all – especially if the feeling of dying is not a turn-on to you.
Christopher Barr

Health & Nutrition Historian

One important study found that high blood levels of selenium is associated with a four- to fivefold decrease in the risk of prostate cancer. Scientists at Stanford University studied 52 men who had prostate cancer and compared them to 96 men who didn’t.[xxvi] One surprising finding was that blood levels of selenium generally decreased with age. It is well known that the risk of prostate cancer increases dramatically as one ages.

Selenium - Geography - Cancer

Those who have studied geographical differences have seen that in low-selenium regions, higher death rates occurred from malignant lymphomas and cancers of the tongue, esophagus, stomach, colon, rectum, liver, pancreas, larynx, lung, kidneys and bladder. Dr. Harold Foster has stated that death rates in the USA for breast, colon, rectal and lung cancer are lower when blood selenium levels are high. Dr. Foster is the one to have reported that cancer patients with low selenium levels tend to have a wider spread of the disease, more recurrences and die sooner.[xxvii] This is critical information that fits rationally into the entire picture of selenium being compiled by medical science and is the principle reason I list selenium as the number four agent in our cancer protocol.

The West African country of Senegal is dominated by high concentrations of selenium in the soil and thus in their foods and as expected we find that Senegalese males had the world's lowest rates for cancer of the trachea, bronchus and lung; stomach and colon; the fourth lowest for prostate cancer and sixth lowest for esophageal cancer. Senegalese women had the lowest incidence of cancers of the trachea, bronchus, lung, esophagus, stomach and colon and second lowest for breast cancer and fifth lowest for cancer of the uterus.

In China, where the selenium levels in the soils varies much more dramatically than in the United States and the population is less mobile, an ecological study in 1985 showed dramatic results in linking cancer with selenium deficiencies. Dr. Shu-Yu Yu measured the selenium content of blood stored in blood banks in 30 different regions in China, and classified the regions as high selenium, medium selenium, and low selenium. They then compared death rates from cancer to the selenium rates and found there was an exact correlation. In the low selenium classification, three times as many people died from cancer as in the high selenium classification.

There is no doubt that selenium is essential for human health and that these elements may protect against cancer and other diseases. For this reason people in regions which are naturally rich in selenium tend to live longer. Selenium, especially when used in conjunction with vitamin C, vitamin E and beta-carotene, works to block chemical reactions that create free radicals in the body (which can damage DNA and cause degenerative change in cells, leading to cancer). Selenium also binds strongly with mercury protecting us from its damaging effects.

Selenium and the Rising Tide of Mercury

Tuna is uniformly rich in selenium. Nearly 300 scientific studies

have demonstrated that this essential element protects against

mercury exposure. Any group carping about mercury in fish

without also talking about selenium is hiding half the story.

One of the main sections in Survival Medicine is about mercury and its toxicity. Although the majority of attention has been given to fish in the media as posing the great health threat in regards to mercury toxicity we have to entertain the possibility that because of selenium, which is an antidote for mercury, fish could be not be as much of a problem as dental amalgam, mercury injected via vaccines, or direct absorption through the air, water and other foods which are becoming increasingly contaminated. The way things are now public attention is focused mostly on fish consumption as the main danger from mercury and this is actually a red herring removing us from focusing on the total threat that mercury has become. It moves our attention away from the combined effects from all sources put together.

The first report on the protective effect of selenium against mercury toxicity appeared in 1967. Since then, numerous studies have shown selenium supplementation counteracts the negative impacts of exposure to mercury, particularly in regard to neurotoxicity, fetotoxicity, and developmental toxicity. The ability of selenium compounds to decrease the toxic action of mercury has been established in many species of mammals, birds, and fish. The detoxifying effect of selenium on mercury toxicity is due to a formation of a biologically inactive complex containing the elements in an equimolar ratio. The complex is unable to pass biological barriers, placenta and choroid plexus and is stored in the liver and the spleen, even in the brain in a non toxic form.

It is well recognized that mercury and sulphur bind together to form complexes. This binding property is the basis of chelating therapy used as a treatment in cases of acute and chronic mercury poisoning. The complexes between mercury and selenium are less generally known but of much higher affinity. Physiologically, sulphur is far more abundant than selenium, yet because of selenium’s higher affinity, mercury selectively binds with selenium to form insoluble mercury selenides. This interaction has been assumed to be a ‘protective’ effect whereby supplemental selenium complexes the mercury and prevents negative effects in animals fed otherwise toxic amounts of mercury.

When selenium and mercury are found together, they connect forming a new compound making it difficult for the body to absorb the mercury separately. Scientists have also tagged cysteine in fish binding with mercury also making it safer to eat. When mercury "binds" to selenium or cysteine it is no longer free to "bind" to anything else -- like brain or kidney tissue.

Selenium deficiency results not only in a decrease of
GSHPx activity, but also in a decrease of GSHPx protein.[xxviii]

Dr. Laura Raymond and Dr. Nicholas Ralston of the University of North Dakota tell us that, “Measuring the amount of mercury present in the environment or food sources may provide an inadequate reflection of the potential for health risks if the protective effects of selenium are not also considered. Owing to the extremely high affinity between mercury and selenium, selenium sequesters mercury and reduces its biological availability. It is obvious that the converse is also true; as a result of the high affinity complexes formed, mercury sequesters selenium. This is important because selenium is required for normal activity of numerous selenium dependent enzymes.”[xxix]

Selenium's involvement is apparent throughout the mercury
cycle, influencing its transport, biogeochemical exposure,

bioavailability, toxicological consequences, and remediation.
Dr. Raymond and Dr. Ralston

Glutathione happens to be the most important of these selenium dependent enzymes. Mercury is highly toxic but mercury’s toxic ruin varies greatly with selenium and glutathione levels. These are the key variables that determine the harm done or the power each individual has to escape the poisonous effect of mercury and other dangerous toxins in the environment. Our defensive shields against both acute and chronic exposure to mercury depend very much on selenium and glutathione.

Selenium is useful as a controlling agent for
mercury, which attacks insulin and its binding sites.

Selenium is a hugely important subject for more reasons than easily meets the eye. Mercury binds with selenium reducing its availability for other functions i.e., for glutathione production in the cells. Thus it is not unreasonable reasoning to see a chain of events starting with mercury contamination passing from mother to child in utero (via mercury vaccines for mother and mothers dental amalgams and fish consumption) stripping the yet to be born of selenium. Newborns receiving more contamination through mother’s milk add to the profile of babies having their selenium levels depleted and thus their glutathione levels set too low to resist childhood vaccines containing thimerosal (fifty percent ethyl mercury) and other toxic elements.

The last 25 years the average daily selenium intake has fallen from 60µg/day to 35µg/day.[xxx] The UK government has established a Reference Nutrient Intake (RNI) level of selenium at 75µg/day.[xxxi] Therefore a nutritional gap now exists between the actual recommended level of daily selenium and what people are actually achieving through their diets. When we calculate in the Rising Tide of Mercury and the extra demands that makes on our selenium stores/nutritional intake we can now see the disaster that has been in the making for decades.

Studies have implicated reactive oxygen species (ROS)
and depletion of intracellular glutathione as major
contributors to mercury-induced cytotoxicity
Sanfeliu et al., 2001

Selenium is absolutely essential in the age of mercury toxicity for it is the perfect antidote for mercury exposure. It is literally raining mercury all over the world but especially in the northern hemisphere. And of course with the dentists poisoning a world of patients with mercury dental amalgam and the doctors doing the same with their mercury laden vaccines, selenium is more important than most of us imagine.

Selenium offers online in real defense time against mercury. As mercury enters our bodies, if there is sufficient selenium it will mop up the mercury before it can bind to its favorite sulfur sites or pass through the blood brain barrier. Taking more selenium reduces the level of "free" mercury doing damage. Minerals and trace elements, the basic building blocks of our bodies, are just not as readily available in our diet as they once were and in the case of selenium this is compounded by the fact that certain vast areas of the world have low selenium contents in the soil and thus the food.

An excess of a toxic metal and/or a relative deficiency of a nutritional
element can be found as significant contributors to every disease.
Dr. Garry Gordon

General Information on Selenium

High doses of vitamin C (over 1 gram ) may reduce the
absorption of selenium. This mineral is best taken one hour
before or 20 minutes after taking vitamin C supplements.[xxxii]

Selenium deficiency impairs thyroid hormone metabolism by inhibiting the synthesis and activity of the iodothyronine deiodinases, which convert thyroxine (T4) to the more metabolically active 3,3'-5 triiodothyronine (T3). In rats, concurrent selenium and iodine deficiency produces greater increases in thyroid weight and plasma thyrotrophin than iodine deficiency alone, indicating that a concurrent selenium deficiency could be a major determinant of the severity of iodine deficiency.[xxxiii]

Later studies showed that serum T4 was maintained at control levels when both dietary iodine and selenium were low, but not when iodine alone, or selenium alone, was low. Activity of thyroidal GSH-Px (erythrocyte glutathione peroxidase) was lowest in rats fed a diet containing high iodine and low selenium. The results suggested that high iodine intake, when selenium is deficient, may permit thyroid tissue damage as a result of low thyroidal GSH-Px activity during thyroid stimulation. A moderately low selenium intake normalized circulating T4 concentration in the presence of iodine deficiency. [xxxiv]

Adequate selenium nutritional status may help protect against some of the neurological effects of iodine deficiency. Researchers involved in the Supplementation en Vitamines et Mineraux AntioXydants (SU.VI.MAX) study in France , which was designed to assess the effect of vitamin and mineral supplements on chronic disease risk, evaluated the relationship between goiter and selenium in a subset of this research population. Their findings suggest that selenium supplements may be protective against goiter.[xxxv] Selenium (Se) in the form of selenocysteine is an essential component of the family of the detoxifying enzymes glutathione peroxidase (Gpx) and of the iodothyronine selenodeiodinases that catalyze the extrathyroidal production of tri-iodothyronine (T(3)). Thus, Se deficiency may seriously influence the generation of free radicals, the conversion of thyroxine (T(4)) to T(3) and a thyroidal autoimmune process.

Recent studies concluded that a positive effect of Se on thyroidal autoimmune process was shown[xxxvi] and indicated that high serum Se levels (>120 ug/l) may also influence the outcome of GD. ( Graves disease). [xxxvii] A recent study testing the various dosages of selenium confirmed that doses greater than 100mcg of selenium (as L-selenomethionine) were required to maximize glutathione peroxidase activities in autoimmune thyroiditis.[xxxviii]

Selenium is also essential for the production of estrogen sulfotranserfase which is the enzyme which breaks down estrogen. A deficiency of selenium can thus lead to excessive amounts of estrogen, which may depress thyroid function, and also upset the progesterone-estrogen balance. Animal studies have shown that the addition of selenium supplementation will alleviate the effects of excess iodine intake.[xxxix] Iodine and selenium deficiencies must both be resolved for iodine treatment to be effective.

Selenium (Se), one of the essential trace elements,
plays a major part in many metabolic functions.

For magnesium to be retained inside cells you need good antioxidant status. Selenium is the main mineral antioxidant. Foods are unreliable because food content is dependent on soil levels of selenium. Foods rich in selenium include whole grains, organ meats, butter, garlic and onion. Seafoods are rich in selenium and obviously not dependent on soil levels.

Ironically, until approximately 40 years ago, selenium was known only as a poison. It is now known that selenium is essential for the normal function of many of the systems of the body and selenium deficiency can have adverse consequences on these systems. Selenium can act as a growth factor; has powerful antioxidant and anticancer properties; and supports normal thyroid hormone homeostasis, immunity, and fertility.

Two of the 22 primary amino acids are distinguished by their possession of selenium: selenomethionine and selenocysteine. Selenomethionine is biochemically equivalent to methionine and is chiefly regarded as an unregulated storage compartment for selenium. In contrast, selenocysteine is tightly regulated and specifically incorporated into numerous proteins that perform essential biological functions.

Selenium, Chromium and Heart Disease

Dr. Majid Ali and Dr. Omar Ali write, “Deficiency of selenium and chromium are established risk factors of IHD. Selenium-dependent antioxidant systems are important parts of human antioxidant enzyme systems, especially in the regeneration of glutathione and other thiol antioxidants. An association between low serum selenium levels and atherogenesis, lipid peroxidation in vivo, and progression of carotid atherosclerosis has been reported. Salonen et al. observed that selenium deficiency was associated with an excess risk of myocardial infarction as well as morbidity and mortality from other expressions of coronary artery disease and other variants of cardiovascular disease in Eastern Finland . In this study, cardiovascular death and myocardial infarction were associated with low serum selenium levels in a matched-pair longitudinal study. Chromium supplementation in patients with type II diabetes results in improved glucose tolerance, lower total cholesterol and triglycerides levels and higher HDL cholesterol levels.”[xl]


Forms of Selenium

The standard of recommended intake levels of selenium is under debate. The UK reference nutrient intake (RNI) is 75 µg per day for men and 60 µg per day for women. The American recommended dietary allowance (RDA), set at 55 µg per day for both men and women. These numbers should be looked at as the bare minimum and do not take into account the increased need for selenium because of the rising tide of mercury in the environment and thus our bodies. Also dosage would be in part dependent on the type of source of selenium used since absorption rates would vary widely.

Back in 1998 Dr. Stephen B. Strum said, “We recommend selenium supplements be given as an organic, rather than an inorganic form. Organic sources of selenium such as selenomethionine, selenocysteine or mixtures of organic forms found in brewer’s yeast have a better safety profile. Recent research indicates higher doses of selenium can be safely given and may possess additional anticancer activity. We currently use daily selenium doses in the 400-800 mcg range in our patients. Other investigators are studying the effects of selenium at much higher doses (1,000-3,000 mcg/day) for prostate cancer and claim to have had little or no toxicity. Clearly, this area is controversial and requires further study.”[xli]

Getting better forms of selenium because of the difference in absorption and bioavailability in the various forms of selenium is a good idea. The Universtiy University of Miami study utilized selenomethionine which has 3 times the bioavailability of the sodium selenite form that is less expensive and more commonly used. Nutritionist Christopher Barr recommends a 100 per cent Whole Food selenium, which he says he has used for decades, from Innate Response which he says has more than 100 times the bioavailability of selenomethionine.

Selenium in its inorganic form is poorly absorbed by the body. Most of the body’s selenium comes from organic sources, where selenium is bonded with sulphur-containing amino acids, the commonest being L-selenomethionine. Many nutritional supplements contain the poorly absorbed inorganic selenium. Selenium formulations containing L-selenomethionine are good choices but the ideal delivery system is provided by spirulina and perhaps by yeasts and even now by probiotics. (This is an area the IMVA is dedicated to studying.) When spirulina is grown in ponds with selenium added, the spirulina absorbs the inorganic selenium transforming it into organic selenium. The selenium becomes protein bonded to the amino acids in spirulina, which are present in abundance.


Selenium is a vital component of the metallo-protein enzyme glutathione peroxidase. This is a major component in the body’s free radical defence system. Thus the availability of selenium is the limiting factor in the production of glutathione peroxidase.

These past two years I have been recommending a natural chelation formula from Science Formulas called Chelorex in part because it is the only chelation formula with selenium. Dr. Alan Greenberg, the developer of this well tested chelator, put together a comprehensive formula that drives glutathione levels higher and mercury levels down. It contains more than several substances on the top ten list of our cancer protocol starting with magnesium, ALA , selenium, and Vitamin C.

Dr. Richard A. Passwater


The following information is provided by Dr. Richard A. Passwater, who has been researching antioxidant nutrients since 1959 and he is the scientist who discovered biological antioxidant synergism in 1962. In 1970, at Toronto , he presented his evidence to the Gerontological Society’s Annual Scientific Congress that antioxidant nutrients offered a practical means of increasing human lifespan. He was the first to show that practical combinations of antioxidant nutrients increase the lifespan of laboratory animals (Chemical & Engineering News 1970).

For this information please go directly to: http://www.healthy.net/scr/Article.asp?Id=577

[i] Hawkes WC, Kelley DS, Taylor PC. "The effects of dietary selenium on the immune system in healthy men." Biol Trace Elem Res. 81, 3:189-213, 2001. www.humanapress.com

[ii] Foster HD. "Landscapes of Longevity: The Calcium-Selenium-Mercury Connection in Cancer and Heart Disease," Medical Hypothesis, Vol. 48, pp 361-366, 1997.

[iii] Turner, R. J. & Finch, J. M. (1991) Selenium and the immune response. Proc. Nutr. Soc. 50: 275–285.[Medline]

[iv] Kiremidjian-Schumacher, L. & Roy, M. (1998) Selenium and immune function. Z. Ernahrungswiss. 37: 50–56.

[v] McKenzie, R. C., Rafferty, T. S., Arthur, J. R. & Beckett, G. J. (2001) Effects of selenium on immunity and ageing. In: Selenium: Its Molecular Biology and Role in Human Health (Hatfield, D. L., ed.), pp. 258–272. Kluwer Academic Publishers, Boston , MA .

[vi] McKenzie, R. C., Arthur, J. R., Miller, S. M., Rafferty, T. S. & Beckett, G. J. (2002) Selenium and the immune system. In: Nutrition and Immune Function (Calder, P. C., Field, C. J. & Gill, N. S., eds.), pp. 229–250. CAB International, Oxford , U.K

[vii] Beckett, G. J., Arthur, J. R., Miller, S. M. & McKenzie, R. C. (2003) Selenium, immunity and disease. In: Dietary Enhancement of Human Immune Function (Hughes D. A., Bendich, A. & Darlington, G., eds.). Humana Press, Totowa , NJ (in press).

[viii] Supplement: 11th International Symposium on Trace Elements in Man and Animals;Selenium in the Immune System John R. Arthur; The American Society for Nutritional Sciences J. Nutr. 133:1457S-1459S, May 2003; http://jn.nutrition.org/cgi/content/full/133/5/1457SOver

[ix] Ryan-Harshman M, Aldoori W. "The relevance of selenium to immunity, cancer and infectious/inflammatory diseases." Can J Diet Pract Res. 66, 2:98-102, 2005.

[x] Nelson HK et al. "Host nutritional selenium status as a driving force for influenza virus mutations." FASEB. 15:1846-8, 2001. www.fasebj.org

[xi] Berg BM et al. "alpha-Tocopherol and selenium facilitate recovery from lipopolysaccharide-induced sickness in aged mice." J Nutr. 135, 5:1157-63, 2005. www.nutrition.org.

[xii] Smith A et al. "Deficiencies in selenium and/or vitamin E lower the resistance of mice to Heligmosomoides polygyrus infections." J Nutr. 135, 4:830-6, 2005. www.nutrition.org

[xiii]Suppression of human immunodeficiency virus type 1 viral load with selenium supplementation: a randomized controlled trial. Hurwitz BE et al; Arch Intern Med. 2007 Jan 22;167(2):148-54; http://www.ncbi.nlm.nih.gov/sites/entrez

[xiv] Packer, L. in Oxidative Stress, Antioxidants and Ageing. Birkhauser, Basal, 1995

[xv] McCloy R. Digestion 1998 (59, suppl. 4) 36-48

[xvi] Kiremidjian-Schumacher. L. et al. Biol. Trace Elem. Res. 1994 (41) 114-127

[xvii] Scott, R and MacPherson A. Br. J. Urol. 1 998 (82) 76-80

[xviii] Finley, J.W. and Penland J.G. J. Trace Elem. Exp. Med. 1998 (11) 11-27

[xix] Pertez, A. et al. Br. J. Rheumatol. 1992 (31) 28 1-286

[xx] http://www.tldp.com/issue/177/ReviciMemoriam.html

[xxi] http://www.healthy.net/scr/Article.asp?Id=2013&xcntr=1

[xxii] Richard A. Passwater, Cancer and Its Nutritional Therapies (New Canaan, CT: Keats Publishing, 1983), p. 149.

[xxiii] http://www.prostate-cancer.org/education/nutrprod/selenium.html

[xxiv] Clark LC. The epidemiology of selenium and cancer. Fed Proc 1985; 44:2584-2590.

[xxv] The role of selenium in thyroid autoimmunity and cancer.Duntas LH.Thyroid. 2006 May;16(5):455-60

[xxvi] The Journal of Urology {2001;166:2034-8}. December issue.

[xxvii] Foster HD. "Landscapes of Longevity: The Calcium-Selenium-Mercury Connection in Cancer and Heart Disease," Medical Hypothesis, Vol. 48, pp 361-366, 1997.

[xxviii] Takahashi K, Newburger PE , Cohen HJ. Glutathione peroxidase protein. Absence in selenium deficiency states and correlation with enzymatic activity. J Clin Invest. 1986 Apr;77(4):1402-4.

[xxix] Raymond, Laura J. Ralston, Nicholas VC. University of North Dakota , SMDJ Seychelles Medical and Dental Journal, Special Issue, Vol 7, No 1, November 2004

[xxx] Food Surveillance Sheet, No 126. London : Joint Food Safety & Standards Group, UK Ministry of Agriculture Fisheries and Food (MAFF), October 1997

[xxxi] McPherson, A. et al. NRC Research Press 1997: 203-205

[xxxii] Am J Clin Nutr. 1989 May;49(5): 862-9

[xxxiii] The role of selenium in thyroid hormone metabolism and effects of selenium deficiency on thyroid hormone and iodine metabolism; Biol Trace Elem Res. 1992 Apr-Jun;33:37-42

[xxxiv] Dietary Iodine and Selenium Interact To Affect Thyroid Hormone Metabolism of Rats; The Journal of Nutrition Vol. 127 No. 6 June 1997, pp. 1214-1218

[xxxv] Selenium Fact Sheet: http://ods.od.nih.gov/factsheets/selenium.asp#h5

[xxxvi] L-selenomethionine substitution suppresses serum concentrations of thyroid peroxidase antibody (TPOAb) in patients with AIT, but suppression requires doses higher than 100 microg/day which is sufficient to maximize glutathione peroxidase activities.

[xxxvii] Serum Selenium levels in patients with remission and relapse of Graves Disease; Wertenbruch T, et al; Med Chem. 2007 May;3(3):281-4.

[xxxviii] Selenium treatment in autoimmune thyroiditis: 9-month follow-up with variable doses. J Endocrinol. 2006 Jul;190(1):151-6. Entrez PubMed

[xxxix] Selenium supplement alleviated the toxic effects of excessive iodine in mice. Biol Trace Elem Res. 2006 Summer;111(1-3):229-38

[xl] Ali M, Ali O. AA Oxidopathy: the core pathogenetic mechanism of ischemic heart disease. J Integrative Medicine 1997;1:1-112. From the Departments of Medicine, Capital University of Integrative Medicine, Washington, D.C., and Institute of Preventive Medicine, New York (MA and OA), and Department of Pathology, College of Physicians and Surgeons of Columbia University, New York (MA).

[xli] Steven Strum the MD author is with the Prostate Cancer Research Institute.
http://www.prostate-cancer.org/education/nutrprod/selenium.html





Dianne Jacobs Thompson  Est. 2003
Also http://legaljustice4john.com
The Misdiagnosis of "Shaken Baby Syndrome" --an unproven theory without scientific support, now in disrepute and wreaking legal and medical havoc world-wide
Author publication: NEXUS MAGAZINE "Seawater--A Safe Blood Plasma Substitute?"

DISCLAIMER: The material on this site is for informational and educational purposes only. Please consult with your health care provider for treatment advice.

EMAIL: Truthquest2


Fight Spam! Click Here!