Zeolite - Articles - Zimbio

Detox- Heavy Metals and Toxins

Sat, 20 Jul 2008 01:03:48 GMT

posted by pg8595

Detox Heavy Metals and Toxins….

With Zeolite

So here we are on my favorite topic. Detoxification with Zeolite. Zeolite is an amazing mineral with the ability to draw heavy metals and toxins into its structure, and be excreted from your body safely. It doesn’t take out any of the electrolytes and minerals that your body needs. This is great news when you consider all of the heavy metals, chemicals and toxins that every one of us is exposed to every day!

If you want to learn more about that read this article Are Toxins Fattenning. You can also visit Let’s Talk Detox for many different current event stories on the shameful pollution of our earth, just in case you are questioning your need to detox. .

There are a number of things that make the Original Liquid Zeolite the best on the market, but first let’s address some facts for those of you who are learning about zeolite for the first time.

What is ZEOLITE?

Zeolite is a unique group of minerals with an important basic property - it’s the world’s only mineral with a naturally occurring negative charge. Therefore, zeolites presently have impressive industrial benefits, and equally impressive Cellular Detoxification implications for human and animal health.

Zeolites possess two intriguing primary physical and chemical properties that are invaluable. These properties include cation exchange and absorption. Zeolites simply lock & hold many positive ions and absorb a multitude of environmental contaminants.

Zeolites were formed from ancient volcanic ash flows settling in neighbouring seas and lakes. This unique group of naturally-occurring minerals has important basic physical and chemical properties and is often referred to as ‘molecular sieves’. Zeolites simply lock & hold many positive ions, absorb a multitude of environmental contaminants and also serve as a catalyst for various processes.

Cation Exchange - Zeolite is the world’s only mineral with a naturally-occurring negative charge. Many positive ions are locked up and held by the zeolite matrix.
Absorption/Adsorption - Zeolite has an open framework molecular structure (very porous) capable of adsorbing and absorbing many different types of gases, moisture, hydrocarbons, heavy metals, low-level radioactive elements and a multitude of other materials. The channels in the zeolite provide a very large surface area where the exchange can take place.

In ENGLISH that basically means that the zeolites have one charge and toxins have an opposite charge. If the toxin molecules are small enough, then the zeolite draws them in like a magnet and removes them!

All ZEOLITES are NOT the same!

Since the original liquid zeolite product hit the market a few years ago, and testimonials started pouring in, manufacturers have rushed to the "drawing board" to try and duplicate the formula, and the success of the product. Now there are several choices of zeolite products in a number of different forms, and mostly you are left to decide for yourself which one is right for you. Following is a description of the different kinds of zeolite products, and their uses.

Powdered Zeolite:
Powdered zeolite is available in a couple of forms. Loose powdered zeolite sold in tubs, or powdered zeolite in capsules.

Powdered zeolites are the simplest to manufacture. Basically, they take raw zeolite, and crush it to a fine powder. The zeolite, which has attracted some heavy metal and toxin deep into it’s cage while in the ground holds on to these compounds and chemicals. It is unlikely that the toxins will be released into your body, however, the already burdened zeolite is less able to pick up NEW impurities than a cleaned "activated" zeolite. Therefore it’s detoxing ability is limited.
The molecules themselves are not small enough to pass through the intestines to reach the blood stream, and into the cells, so it’s action is confined to the gut. Impurities, toxins, herbicides and pesticides on the food you eat, and viruses or bacteria in the intestinal tract may be absorbed by powdered zeolite.

Powdered zeolite may be very effective as an anti-diarrheal agent, and for upper G.I. distress such as heartburn and reflux. Zeolite is approved as a drug in Cuba under the trade name ENTEREX for exactly such a purpose.
"Liquid" Zeolite:
First a note about the name "liquid". the zeolite itself is not liquified. In fact "Liquid" zeolite is actually a solid zeolite in suspension. The zeolite ‘floats’ in the water, allowing for even distribution of the zeolite molecule in a liquid. In the "zeolite in liquid" category there are several different choices.
- "Enhanced" Zeolite:
  Enhanced zeolite is so called because it is "enhanced with vibrational energies". I am not exactly sure what that means and their website does not shed any light on that. There is no way to "enhance" a product with "vibrational energies" in any kind of scientific way. I understand that holistic healers talk about vibrational energies, but we are talking about living things, and once living foods and supplements. Zeolite is a mineral. It DOES naturally have a charge which attracts like a magnet opposite charged molecules. Most of the toxins introduced to our cells have an opposite charge to the zeolite, but changing the charge alters the property that makes it work in the first place.
  It seems "enhanced zeolite" products are not cleaned out before they go to market either. This means they harbor levels of heavy metals, and toxins in their cages. Again while it is UNLIKELY that the toxins will be released into your system, the zeolite molecules are less effective if they are already burdened.
  
  A disturbing note on "enhanced" zeolite… it seems that the website Cancer Fighting Strategies.com is promoting a enhanced zeolite as the "best" and they offer a number of patient testimonials to support this. However, it seems that the testimonials are actually from people who used the Original Liquid Zeolite from Waiora. You can read more about that at Zeolite Canada
- Zeolite in Humic acid:
  The introduction of humic acid into a product is one company’s attempt to have the zeolite suspended in water. The ORIGINAL product uses a patented process to suspend (float) the zeolite particles which would normally settle to the bottom. Z Life brand and other humic acid brands are not privy to the process, so humic acid is introduced to get the particles of zeolite to float.
  
  From their site Humic Acids are biological compounds created by Mother Earth. We call it "mother’s milk from the earth." These composites were originally deposited by pristine, ancient forests and compacted and transformed over millions of years, waiting to be extracted for our use today. Translation…. humic acids come from rotting leaves. (seriously… look it up! :o) They mention on the site that Waiora uses heat and chemicals in the processing.. this is true. Waiora uses a heating process followed by a mild acidic bath (something like vinegar) to clean the cages so you get a pure product free of poisons deep in the cages. Heat doesn’t hurt the zeolite. Rememebr,it comes from Molten lava! Waiora is hot but not THAT hot!
- The Original Liquid Zeolite:
  The purest most effective zeolite supplement on the market. Pure clean cages make it the most effective at cleaning your cells, while the suspension technology ensures that it is evenly dispersed throughout the bottle. Each drop is the same as the last. The zeolite is small enough to pass through the gut into the blood stream. Toxins are grabbed and removed safely and efficiently with little side effect. There are no worries of contamination from organic debris, no question of effectiveness due to being unclean, and no end to the number of testmonials on THIS product. In fact, ALL of the testimonials I have seen on the internet thus far have been testimonials from people using the Natural Cellular Defense product, EVEN when a different product is being sold. I haven’t seen any original testimonials on the other products.
  
  I have done a significant amount of research on this product. I wouldn’t trust my health to any other zeolite product.

If you want to learn more about zeolite (and there is LOTS more to learn) grab my free book by clicking The Liquid Zeolite Book or just go over there and click on the book cover for The Liquid Zeolite Book under Life Books!

Many Blessings,

Shelley

Liquid Zeolite Testimonial

Thu, 4 Jul 2008 12:39:36 GMT

posted by donnavaldes
Why am I involved with Waiora, because Waiora changes lives.....check this out...
"My name is Mandy and I've been with Waiora since June of 2006. Now, when I first got on the Natural Cellular Defense, I got on it for a reason that was other than the type one diabetes that I deal with. But after I had been on Natural Cellular Defense for about two full months, I went through probably about a 7 - 10 day span of time where I really honestly believe that the Natural Cellular Defense had caused my pancreas to start functioning and producing insulin.

Now, when I was first diagnosed with diabetes back in 1965 the doctors told my parents that my pancreas wasn't completely shut down. It would start up every once in a while for about a 24 hour span of time. And that had happened over the years, but it had been a long time since that has happened. But after I had been on Natural Cellular Defense for about 2 months, about 8 weeks, I was amazed that I went through the 7 - 10 day span of time where I couldn't get my glucose levels up above the forty's. I mean, this was morning, afternoon and evening.

I remember the feeling that I had, and that feeling was very similar to the previous times when my pancreas had started before, and I thought ‘Wow, is it a possibility that my pancreas could be starting?' And, I have to say that now, my pancreas isn't completely functioning yet, but I do take a very small amount of insulin and my hemoglobin A1C levels are somewhere between 6.0 and 6.5. I'm real thankful for what this product has done for me, and I hope that this can be of some use to other people and also be helpful to other diabetics. Have a good day. Bye-bye."

Head over to www.DetoxWithZeolites.com and check out the incentive where I give away free NCD.

Take care
DonnaDonna Valdes is a "self-retired" corporate executive who left abandoned her career to work from home. She is an author, mentor and homebusiness coach. Her interests in toxins started when researching a product launched by her company. She realized how ignorant she was about toxins and how they affect her family and began her blog to help educate others. You may contact her online at donnavaldes.com or toll free at 888-658-8778.

Chelation therapy- EDTA, DMPS, DMSA, or Zeolite - Let's compare

Sun, 19 Nov 2007 02:50:10 GMT

posted by pg8595
We live in a toxic world... well I think that has certainly been established. There are a number of different options, though, when evaluating therapies to remove toxins and heavy metals from the body. This article from The Heart Fixer (which is the welcome page for the clinical and research websites of Comprehensive Heart Care and Cardiologist James Roberts) explains them in great detail. Dr. Roberts is NOT associated with Let's Talk Detox. I simply found him on the web while researching and thought you would enjoy the information. Please visit The Heart Fixer for more information about Dr. Roberts and the services he provides.

Dr. Roberts has been providing his patients with chelation therapy (CT), in all of its forms, for 10 years. He passed the written exam of the American Board of Chelation Therapy in 1986 and has participated in the training of other physicians in this technique. Ten years ago there was only one approach to CT, the three hour infusion of Mg-EDTA. Today we have multiple chelating agents, many of which can be administered in more than one way. It will be Dr. Roberts' job to evaluated your need for CT and then to recommend a treatment program tailored to your individual health needs. Basic concepts, EDTA, DMPS, DMSA, and Zeolite will be discussed.

Chelation Therapy - The Basic Concept:

Heavy metals, such as lead, cadmium, arsenic, and mercury, poison key enzyme systems and play a key, causative role in the degenerative, age related disease states that plaque Western society. Our bodies were not designed to deal with these toxins (neither evolution or our maker anticipated the toxic metal exposure experienced by mankind today). We do a poor job of removing them, such that these toxins accumulate over our lifetime. When we are young and healthy we can handle this toxic stress, sequestering the toxins in intracellular dust bins (unless we are genetically predisposed to heavy metal toxicity, such as in the situation of Autism), but eventually our intracellular dump sites overflow, our enzymes systems begin to fail, and then we get sick. This starts with age-related conditions such as hypertension and hyperlipidemia, or we may feel tired for no good reason. In later years metal toxicity may show itself in disease states that end our lives, including heart disease, cancer, or the neurodegenerative diseases associated with advanced age. CT involves the administration of agents that will bind to the heavy metals stored within our body and then escort them out, via the kidneys or GI tract. The goal of CT is to "de-poison" you. While patients typically become interested in CT only when they suffer from an advanced disease state and no other options are available to them (basically because insurers will not cover the cost of CT), the best time to begin CT is well before your get sick. To us, CT is a no-brainer. We feel that CT is one of the most important thing that we can offer you. Standard medicine offers you drugs and surgery, as do we, but it just doesn't make sense to us to drug you and operate on you without at least attempting to detoxify you.

Chelation Therapy - Which approach is best for you?

Good question - the answer will depend on:
A. The types of metals you have on board.
B. Their tissue levels; stated otherwise your toxic burden.
C. Your concomitant medical conditions.
D. Your preference as to route of administration, how quickly you wish to be detoxified, and cost factors.

Our best measure of tissue or body metal burden is the provocative challenge study. It would be neat if your blood level of a specific toxic metal reflected your body burden of that metal, but this is not the case. The correlation between blood and tissue metal levels is limited. We also know that "normal" blood levels of toxic metals are associated with disease states The average or mean blood lead level in American adults is 3.6 ug/dl, and anything below 10 is considered to be "normal". But if you compare American adults with blood lead levels in the upper tercile (top 1/3rd), with levels above 3.6 ug/dl, against those whose levels are in the lower tercile, with levels below 1.9, and follow their course over 12 years, you find that the high normal lead individuals are 25% more likely to die than are their lower lead colleagues. Their 12 year relative risk for death due to heart attack, stroke, or cardiovascular disease in general, in comparison to the lower lead group, are 1.9, 2.5, and 1.5. That's a lot of disease and death associated with blood lead levels well within the normal range. Our conclusion is that there is no normal range for lead; we want to get lead, and any other toxic metals that are in you, our of you. Kids with a blood lead level of 10 have IQs 7 points lower than kids with levels of 0-1 (for more on lead, please look in the medical topics section).

The most accurate means of assessing your body burden of a given toxic metal would be to biopsy your brain, heart, kidneys, and liver - obviously not practical. Instead we carry out a "biochemical biopsy" or Provocative Challenge - we administer to you a chelating agent, a drug or nutritional agent that binds to, and then removes via the kidneys, the toxic metal in question from your system, and then measure its concentration in a subsequent six-hour urine sample. The amount of metal that we see in the urine sample, your "metal spill", will be a function of your body burden of this metal, the integrity of your excretory routes, the specific chelating agent that we administer, and its dose. EDTA binds avidly to lead within your system, but not to Mercury. If we are interested only in lead, we would carry out an EDTA challenge. We would administer 3,000 mg of IV EDTA, then measure the amount of lead excreted over the next six hours. We would see lead, cadmium, a few other metals, but negligible amounts of mercury. We would not see much mercury, no matter your body burden of this agent, because EDTA does not bind to mercury. If we were interested only in mercury, we would carry our a DMPS challenge. Here you would receive 3 mg/kg of DMPS, which binds tightly to mercury, and less avidly to lead. Your urine sample would likely demonstrate an appreciable amount of mercury, and not much lead. If we administered only 1.5 mg/kg of DMPS, we would see a smaller mercury spill, just as we would see less lead if we gave you 1,000 mg as apposed to the usual 3,000 mg of EDTA. DMSA, an orally administered agent, will bind to lead, cadmium, and mercury, but less avidly than would EDTA or DMPS. Comparing metal levels in a post-EDTA urine specimen to the metal spill following EDTA or DMPS would be inappropriate, really an apples to oranges comparison. What we do is to carry out a "triple challenge", administering to you a panel of chelators, each in low to moderate dose, to give us an estimate of your body burden of all the metals of interest to us. For two days you take an oral agent that contains EDTA and garlic (Essential Daily Defense - EDD). On the day of the triple challenge you take a double dose of EDD, then we administer to you 500 mg of oral DMSA, along with 1,000 mg of IV EDTA and 125 mg of IV DMPS. The level of toxic metals in a subsequently collected 6 hour urine specimen serves as our best measure of your body burden of these agents, and will shape the chelation program that we design for you. We will repeat the triple challenge study periodically, using the results to make adjustments in your program, such as when to switch from one chelator to another or whether to switch from active therapy to maintenance chelation, always using the same protocol, allowing for an apples to apples comparison. This is our best methodology but it's not a perfect methodology. Some people with high body metal burdens spill little metal on their initial challenge study. The problem is that they are so poisoned by metal, or so sick in general, that the enzymes involved in basic detoxification and excretion are shot. If we chelate these people for a period of time, and/or take other measures to improve their health, we will typically see a greater spill of metals with subsequent testing. Thus it is not unusual for your challenge report to look worse after a period of chelation. Your metal burden has not increased; what has increased is the functional integrity of your enzyme systems and excretory routs. The determination of your toxic metal body burden is the most important factor in determining our chelation prescription for you, but we will also take in to consideration your specific health care needs, your preferences, and cost factors. The diagnostic Triple Challenge is also discussed on the Diagnostic Studies Available page. Representative challenge findings are presented at challenge results.

Now lets examine the individual chelating agents in common use.

IV EDTA, short for ethylene diamine tetraacetic acid, binds avidly to lead and cadmium, less tightly to aluminum and arsenic, and only weakly to mercury. EDTA administered orally is poorly absorbed; only 2-4% of a given dose will enter the bloodstream. Oral EDTA works by binding to metals dumped into the GI tract by the liver, blocking their reabsorption from the gut back into the circulation (more on this later). EDTA given orally is thus a relatively inefficient approach to chelation therapy; oral EDTA works - it will decrease your body burden of lead, cadmium, and other metals that EDTA can bind to - but it works only slowly. Oral EDTA is used as an adjunct to IV chelation therapy, or as a preventive. Oral EDTA alone is not an appropriate mono-therapy for a sick patient with a heavy body metal burden. On the other hand, EDTA administered IV is an extremely efficient metal chelator. Standard chelation therapy, as it has been practice over the past 50 years, involves a 3 hour infusion of EDTA bound to magnesium (Mg-EDTA). Included in the IV bag will be 5,000 mg of vitamin C, B vitamins, and folic acid. Mg-EDTA removes toxic metals, provides anti-oxidant protection, addresses homocysteine, and provides vitamin C (see vitamin C literature review in the medical topics section) and magnesium, two key nutritionals lacking in the patient with cardiovascular disease and hypertension. We favor IV Mg-EDTA over IV Ca-EDTA for the metal overloaded patient whose primary problems are vascular insufficiency and/or hypertension. While Mg-EDTA requires a 3 hour infusion, Ca-EDTA can be administered over 5-10 minutes. Ca-EDTA does not provide magnesium, vitamin C, or B vitamins, all it provides is EDTA for metal detoxification, but here it is a little more efficient than is Mg-EDTA. We favor Ca-EDTA over Mg-EDTA when hypertension or atherosclerotic vascular disease are not major problems, or for the patients who cannot give up 3 hours once a week for the Mg-EDTA infusions. We typically carry out 20 to 30 IV Mg or Ca-EDTA treatments, and then repeat the triple challenge to monitor progress. IV EDTA is typically administered once a week, but if we are not in a hurry then every two week dosing is OK. We will always recommend oral EDTA as an adjunctive treatment when we treat you with IV EDTA - here's why - I will use lead as an example but the principles apply to all toxic metals. While we do not do a good job of clearing lead, we do try. The liver will filter lead from the circulation and from the food that we ingest. The filtered lead is secreted by the liver cells into bile, which is excreted by the liver into the GI tract, from there expelled into the stool. Lead itself is not water soluble, so the liver cells bind it to a glutathione, so it is actually the water soluble lead-glutathione complex that is excreted into the bile. The problem with this process is that the bond between glutathione and lead is not very tight. If our GI tract is functioning smoothly, the lead is excreted in the stool, but if our GI tract is sluggish, the typical situation in American adults, the lead-glutathione bond breaks before the lead can be excreted. When this happens, the lead is reabsorbed into the bloodstream, while the glutathione molecule is lost in the stool. The reabsorbed lead can be re-filtered by the liver, re-bound to a new glutathione molecule, dumped into the gut, and then reabsorbed. This process accomplishes nothing except for depletion of the liver's glutathione stores. This is a disaster, as glutathione is not only a detoxifier, it is also the primary antioxidant in our system (this is why metal toxicity is so dangerous - the metals poison us and at the same time our futile attempt to remove them weaken us further). However, if we happen to have EDTA in the gut (and 96% of the EDTA that we take in orally will remain in the gut), any lead dumped into the gut by the liver (glutathione-bound or free because the glutathione-lead bond broke) will be immediately scarfed up by the EDTA, and taken out with the stool. Oral EDTA thus converts our innate, relatively inept and self-injurious lead detoxification system into an efficient and effective lead detoxification system. Oral EDTA will also bind up any lead that you take in with your food and water. Concomitant oral EDTA greatly enhances the efficacy of the EDTA that we administer IV, be in Mg or Ca-EDTA. Our standard recommendation is that you take EDD (Essential Daily Defense - oral EDTA, garlic, and several complementary agents - formulated by Dr. Garry Gordon, a leader in the field of chelation), 2 to 6 capsules each day, increasing to 6 to 12 capsules the day before and the day of your IV EDTA treatment. In this fashion we get more metal out, and we improve your tolerance to the EDTA administered IV (When we administer EDTA IV, it binds to lead and most of the EDTA-lead created is excreted via the kidneys into the urine, but some goes out via the liver, from there to re reabsorbed into the circulation, making you feel poorly the day after you receive IV EDTA. However, if you also receive oral EDTA, the lead will not be reabsorbed into the circulation.).

DMPS and Transdermal DMPS-Glutathione

EDTA, the metal binding agent used in classic chelation therapy, binds avidly to Lead, Cadmium, and several other metals, but it has little activity against Mercury. Stated otherwise, EDTA does a poor job of removing Mercury from your body. I don't care is you have received 100 IV EDTA treatments - EDTA simply will not get the job done if the job is to remove Mercury. DMSA, an oral agent, can bind to all three of the above metals, but only weakly. Our most effective Mercury scavenger is DMPS (2-3-dimercaptopropane-1-sulfonate):

DMPS is a di-thiol chelator. Mercury binds, in a nearly irreversible fashion, to thiol groups (-SH) of intracellular structures, such as proteins, enzymes, and DNA. The Mercury damages the structure, and just doesn't let go of the thiol group. This is why Mercury toxicity is cumulative. Mercury can get in to your body with relative ease, but on its own it leaves only slowly. To remove Mercury that is "stuck" to a thiol group, we need to present to the bound Mercury something that it can bind to tighter than one thiol group, such as two thiol groups. The di-thiol chelators, DMPS and DMSA, can pull Mercury off its thiol binding site, and then escort it out of the body. DMPS is poorly absorbed when given orally. Up until recently our approach was to administer DMPS IV, at a dose of 3 mg/kg, up to 250 mg, once a week, with periodic monitoring of the post-DMPS urine Mercury level. This approach was rather expensive, and cumbersome with the need for frequent IV treatments. IV therapy certainly doesn't lend itself well to the treatment of Autistic kids, the majority of whom are Mercury toxic.

Glutathione plays a role in multiple physiologic processes (to liberate one molecule of Nitric Oxide from the sublingual NTG that is taken for angina, one molecule of Glutathione is used up). Glutathione serves as our primary intracellular antioxidant, antioxidant recycler, and detoxifier, and has been demonstrated to be of therapeutic value in certain neurological and cardiovascular conditions. Glutathione can reduce Mercury from its oxidized form, which binds tightly to intracellular structures, to its reduced form, which is easier to mobilize. Co-administration of Glutathione enhances the ability of DMPS to clear Mercury.

The problem with both DMPS and Glutathione, to date, has been their poor oral absorption. IV administration has been required, with its attendant costs and logistical limitations a problem. To solve this problem, Dr. Rashid Buttar developed TD-DMPSÔ, a 4:1 ratio of Glutathione and DMPS complexed within liposomes, tiny spherules of fat soluble phosphatidylcholine, which are easily absorbed through the skin. Dr. Buttars thinking has moved us from IV to a transdermal delivery system for these most effective agents. Both are now absorbed through the skin, enter the circulation, and act as is they were slowly dripped in via the IV route. TD-DMPSÔ is available through AMT pharmacy (a division of College Pharmacy) in N. Carolina (866)-828-8203, as a compounded prescription. We fax a prescription, along with your demographic information, to AMT, and they ship the Transdermal DMPS-Glutathione to you. It is your responsibility to re-order this material when your supply runs low. We have no financial relationship with AMT pharmacy. Writing up all these prescriptions and sending out the faxes is simply part or our overhead so please make it easy for us to help you.

The side-effects of TD-DMPSÔ are typically the side-effects of Mercury detoxification. Many patients feel nothing, while others experience fatigue, irritability, muscle aching, or possibly a transient aggravation of the symptoms that we feel are due to Mercury overload. Minor symptoms can be ignored, but if you feel poorly, simply decrease the dose (such that less Mercury will be mobilized) to a level that you can tolerate. Later try to slowly increase the dose to the target level. As more Mercury is removed, tolerance to treatment typically improves.

We are in no hurry here. Patience is required. At age 50 we are trying to undo 50 years of progressive cellular Mercury overload. We are not going to get the job done in 2 months. Removing 50 years of Mercury is like peeling off the layers of an onion. To monitor progress, periodic challenge studies will be carried out (measuring urine metal levels following the administration of IV chelators), and we will be monitoring your symptomatic status as well.

It is my belief that many of the degenerative, chronic disease states that plague us today are due to, or aggravated by, intracellular heavy metal overload. These toxins bind, nearly irreversibly, to intracellular structures, inactivating them. Mother Nature never anticipated that her children would be exposed to these toxins, so our ability to clear them is limited. For example, it is estimated that, without medical intervention, it takes 20 years for brain Mercury content to fall by 50% following removal of the source of the Mercury. The medical and scientific literature is full of references linking toxic metals like Mercury, Lead, and Cadmium to the diseases of today.

Before beginning a program of metal detoxification, first begin a program of antioxidant and mineral supplementation (a dedicated 6-a-day preparation, 2 tabs with meals); I may recommend other supplements as well, depending on your overall condition. It is critical that you have a chelator in your blood stream when your Mercury Amalgam fillings are removed; coordination between the Doctor and the Dentist is important. Do not take a metal detoxification program if you are pregnant or nursing. Keep up with your mineral supplements, but do not take minerals within 6 hours of a TD-DMPSÔ application (DMPS binds as tightly to Zinc, Copper, and Chromium as it does to Mercury). 5% of patients will experience a rash at the application site. This will resolve on its own; the best approach here is to rotate the application site. If you develop an infection, hold TD-DMPSÔ until the infection resolves. If you feel poorly, lighten up on the dose for awhile and take extra minerals. If that doesnt work, give us a call during office hours or move up your follow-up appointment. We have found that DMPS and other metal chelators work best within a negative field magnetic environment (see discussion in Magnetico sleep pad and oral DMSA in preparation for MME on the MME site).

DMSA, like DMPS, is a di-thiol chelator. Unlike DMPS and EDTA, DMSA is well absorbed. DMSA is not a very powerful chelator, but taken over a period of time, particularly within a magnetic environment, DMSA can provide you with effective chelation. In the doses that we utilize (500 mg once or twice a day) side-effects are rare. Rash can occur, most likely on the basis of Mercury detoxification through the skin. Kidney and liver toxicity in this dosing range is quite unlikely. DMPS, more powerful than DMSA, does not get into the nervous system, while DMSA does. Many clinicians recommend "de-bulking" the Mercury with DMPS, then finishing up the job with DMSA. However, we have seen an improvement in neurological function following the use of DMPS-Glutathione, especially in Autism. It may be that DMPS does such a good job of removing Mercury from the rest of the body that a "concentration gradient" for Mercury is created, such that Mercury is "drawn out" of nervous tissue following the gradient. Dr. Bonlie, the inventor of the MME device and the world's expert of magnetic chelation, prefers DMSA over DMPS, and we use DMSA as our chelator of choice during MME treatment. I have become comfortable with the use of Transdermal DMPS-Glutathione, and prefer this compound to DMSA, particularly in kids with Autism. IV DMPS is now used only in the context of triple challenge or DMPS/DMSA Mercury challenge studies. Mercury and DMSA are discussed further in the Medical Topics section of this website.

Zeolite, technically a mineral, consists of alternating Silica Tetra Oxide and Aluminum Tetra Oxide crystals that arrange themselves in a lattice-like configuration. The compound has a negative electrostatic charge, while toxic heavy metals have a positive charge. Zeolite thus provides an extensive negatively charged surface area that can attract and bind negatively charged toxic metals. The Zeolite-metal complex is then excreted from the body. The Aluminum is locked in to the Zeolite structure and is not retained within your body. Zeolites have been used extensively in water processing, have been shown to be of value in bacterial diarrhea (it binds to bacterial toxins too), and are now being used in animal and human detoxification. Zeolite is less potent a chelator than are the chemical agents such as EDTA, DMSA, and DMPS, and we do not have a long-term track record with the use of Zeolite in chelation therapy, but this material appears to be quite safe. Zeolite makes chelation therapy affordable to everyone. I think this is important. I feel that every adult American should be on some form of ongoing, low-level chelation therapy. I feel this way because I know that every American adult is loaded with toxic substances. I'd prefer to get this garbage out of you before you become ill, but you don't want to do this, either because you do not understand the importance of detoxification, or because of the cost and time commitment associated with the IV chelation techniques. Well, nobody is too busy to take one teaspoon of Zeolite in water or juice every day, and nearly all of us can handle the low cost per month over one to two years of Zeolite chelation. We often use Zeolite along with DMSA during MME. We recommend that you take Zeolite on an empty stomach, 1-2 hours away from food, minerals, or prescription agents.

IV EDTA and DMPS are pharmacologic agents and can be administered only by a licensed medical practitioner. DMSA can be obtained over the counter or by prescription. Oral EDTA and Zeolite are considered to be supplements and are available only over-the-counter.

DeToxMax - DeToxMax consists of EDTA, magnesium, and lipoic acid admixed with microencapsulated Phosphatidylcholine. DeToxMax provides an effective oral delivery system for EDTA and Phosphatidylcholine, the two most important molecules in nutritional cardiology. For more information and case studies please click on DeToxMax.

Chelation Safety Issues - Chelation therapy is safe.

Remember, we are taking poisons out of you, not putting poisons in (which in a sense we are doing with drug therapy). Still, there are issues of patient safety and treatment tolerance that we should address. The chelating agents that we administer to you do not stay in your body. They bind their target metals, and then the metal-chelator complex exits the body via the kidneys or GI tract. It is possible to overwhelm the body's excretory routes with too much metal. Let's say that you are loaded to the gills with lead, and you already have some pre-existent kidney damage. If we gave you a large dose of IV EDTA, we could mobilize far more lead than the already dysfunctional kidneys be handled. Some of the lead could get "biochemically stuck" within the kidneys and kidney function could be compromised. If we did this over and over, without checking on kidney function, we could damage the kidneys. On the other hand, studies have shown that EDTA chelation actually slows down the rate of kidney deterioration in chronic kidney disease (see Lead discussion in the Medical Topics section of this website), and this has been our experience as well (see Case Study - Kidney function improves with chelation). The key point here is to administer the EDTA in a slow and steady fashion, at a dose that the kidneys can handle. We will determine your dose of EDTA as a function of you body size and your baseline kidney function, and we will monitor your kidney function with periodic lab studies, and then adjust your EDTA dose accordingly. If we add a new drug that might affect kidney function (say a diuretic, ACEI, or spironolactone for heart failure), then we will recheck your kidney function to determine if a change in your EDTA dose is appropriate. If another Doctor changes your drug regimen, please let us know, as this may influence our decision making as well. We may recommend that you take nutritional agents that seem to help kidney function, such as asparagus extract or N-Acetyl Cysteine. While chelation therapy with EDTA does not affect liver function, some of the EDTA-metal is removed via the liver; to support liver function we may recommend Mild Thistle Extract (Silymarin) and N-Acetyl Cysteine.

Detox Reactions and Patient Tolerance - Some people are so toxic that when we mobilize the offending metals they experience a "detox reaction". They feel poorly, with muscle aching, fatigue, and nausea. Mercury overloaded individuals may experience a rash or irritability. While you certainly are not enjoying your detox reaction, it does mean that we are barking up the right tree. These metals do need to come out, but of course we do not want to torture you in the process. What we do here is to slow down the process, decreasing the dose of your chelator, and/or increasing the time interval between treatments. We may administer 1 or 2 IVs containing vitamin C, minerals, and glutathione, without a chelator. Symptoms occurring the day after chelation are typically related to GI re-uptake of metal-chelator complexes cleared by the liver into the gut (see discussion above). Here we increase the oral component of your program to help trap the toxin within the GI tract. Muscle aching and muscle spasms typically reflect mineral deficiency. The chelators bind preferentially with toxic metals, but they can bind to and remove from your body nutritional minerals as well. All patients receiving chelation should be on a 6-a-day vitamin and mineral supplement. We ask you to "divorce" the minerals from your chelation. Take your minerals as far apart from your chelator as is feasible. Do not take oral minerals on the morning of IV EDTA; take them that night instead. If you are applying transdermal DMPS-Glutathione at bedtime, get your minerals in by dinner that night and start up again at noon the next day. If you do take your minerals and your chelator at the same time, nothing will go wrong, but the chelator may bind up the nutritional mineral that you just took. You won't get the benefit of the mineral, and you won't get the benefit of the chelator. If you do experience muscle aching, the first thing to do is to increase your mineral supplementation.

Costs and Politics - Your insurer will not cover chelation therapy. Many will say they do, and they may even put this in print in their brochures, but they will not cove the cost of your chelation. When pushed they will say that your chelation was "medically unnecessary". You can appeal, and a doctor who knows nothing about chelation therapy, a doctor who works for the insurance company, will review the records and tests that we send in and conclude that it was "medically unnecessary". There is nothing that we can do about this and the insurance companies know this. They may insist on an elevated blood lead level to confirm the diagnosis of lead or mercury overload. Anyone with even a passing knowledge of the scientific literature will tell you that blood levels do not correlate well with body metal burden in adults but your insurance company will still insist on a blood lead level. I will not bill your insurer for chelation therapy administered in my office. I do not care what they say in their literature. If you want to undergo chelation therapy and have it billed to your insurer, please have your chelation therapy done elsewhere.

I was taught by my professors that chelation therapy was ineffective and that its practitioners were "quacks". I believed this and as a young doctor I parroted this nonsense. It wasn't that I was stupid. It wasn't because I was arrogant (well maybe a little). It was because going in to medical school/residency training, we soon-to-be physicians know nothing and we believe what we are told by our teachers. It really takes being out in the real world for 10 years to see that not everything that we were taught is correct. My "awakening" to the benefits of chelation therapy in cardiovascular disease is discussed in Reverse Heart Disease Now. Briefly, a number of my personal patients underwent chelation therapy behind my back and got better. They got a lot better. It was embarrassing. So I learned how to do it so more of my patients could get better. Some inoperable patients got better. My colleagues did not appreciate my new skill, or the direction I took back then to bring my practice to where it is now. I lost the friendship and respect of everyone (doctors, nurses, hospital administrators) who I had worked closely with for a decade. Patients left my practice, because they were told that I was a "bad doctor". Social friends learned that I was a "dirty doctor". Old friends began to shy away from me at our kids little league games. Lies and juicy half truths were sent in to the Medical Board. I stuck to my position as I was doing nothing wrong. No actions were taken against me. I am 51 years old and have never been sued and have never been sanctioned (I was an Eagle Boy Scout so what do you expect!). I weathered the storm and am now stronger and smarter than I was back then. So please do not expect me to defer to the wishes of practitioners who have not had a new thought in their head over the past decade. Do not expect me to put politics ahead of science. Do not expect me to compromise my judgment just to get along. On the other hand, if you want to pick a fight with your other doctors or with your insurance company, do not try to drag me in. Do not expect me to chelate you if any of us feel that chelation might compromise another, ongoing treatment. Do not expect me to chelate you "on the sly", without the knowledge of your other doctors. Do not expect me to chelate you for free. I did not render you metal toxic, so I have no obligation to detoxify you for free. I will be up front with you and you must be upfront with me - basically we all have the follow correct principles.

James C. Roberts MD FACC
12/07/06

My Note - I really really like this doctor from reading the last 2 paragraphs which show such a human side. As a "retired" cardiac care nurse, I know only too well how rare this is in a cardiologist. I have included many links to Dr. Roberts website (and one to his book), but in case you missed them, please visit http://www.heartfixer.com/

Waiora International Boasts a Recent 1000% in Growth: What is Driving This Growth?

Fri, 20 Oct 2007 22:17:47 GMT

posted by donnavaldes
Here is a press release that was awhile ago, I found it on Google and thought it would be cool for my blog.
Take care,
Donna
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Why it is Natural Cellular Defense, For The Next New Buzz Word -- Detox

Waiora International is one company leading the charge in detoxification. Their newest product, Natural Cellular Defense, is creating such a stir in the direct sales and network marketing industry, that their growth has seen a 1000% increase since the product's launch in August, 2005. Waiora and NCD are attracting key industry leaders such as Donna Valdes. Valdes shares her insight into why this liquid cellular zeolite is today's hot ticket item.

Tampa, FL (PRWEB) April 22, 2006 --It's no secret; our aging population of baby boomers has dictated our market place for years. When we were in our 20's, we were excited about sports nutrition and fitness. Then gender specific nutritionals were the rage. As we aged, we were enlightened about our poor nutrition, and have tried every fiber, shake, pill and juice we could find to supplement our diet. It seems the next phase is detoxification. As we all know, toxins inundate the air we breathe, the water we drink and the food we eat. They are responsible for creating and enhancing the most common and debilitating diseases today. Waiora International is one company leading the charge in detoxification. Their newest product, Natural Cellular Defense, is creating such a stir in the direct sales and network marketing industry, their growth has enjoyed a 1000% increase since the product's launch in August, 2005. Waiora and NCD are attracting key industry leaders such as Donna Valdes. Valdes shares her insight into why this liquid cellular zeolite is today's hot ticket item.

Waiora started in April 2004, but it was a vision long before then. Each member of the management team has extensive experience with other direct selling companies, most notably Rexall Showcase International. Combined, the management team possess more than 70 years of experience in the direct sales industry. On the day this company was launched it was running like a veteran company. The team understands the industry and perhaps most importantly, the needs of their Independent Distributors. This is one reason Valdes chose Waiora as their new home based business venture. A good company story is only half the equation to solid, fast, success. Valdes feels you need a great product to fuel volume and she was most impressed with Waiora's cornerstone product, Natural Cellular Defense, their cellular zeolite product.

What is Natural Cellular Defense and why has it driven volume like no other product in direct sale and network marketing history? NCD boasts of a unique crystalline structure of zeolite which makes up the active ingredient in the product. Zeolites are found in nature and are formed by the fusion of glass-rich volcanic rock with water (either fresh water or seawater). These zeolites have a rare property of being able to exchange positively-charged particles with surrounding elements without losing their structure. Zeolites are, basically, negatively-charged minerals. Most impressive is the ability of the zeolite crystal to act as a "cage", trapping particles and compounds and isolating them from the biochemistry of the organism. Because of this unique mechanism, this product offers a unique line of defense that compliments existing nutritional therapies without redundancy. NCD is proprietary to Waiora for its activation process which makes the cage-like molecule clean when ingestesed and specific for what it removes from the body unlike other zeolites or chelating agents. The liquid delivery system of NCD also makes it unique and very easy to use and share. Valdes was attracted to the exclusive distribution rights to NCD.

Waiora's future looks bright. Waiora is working closely with Valdes and her team of business developers, which specializes in international growth to help expand Waiora into Canada, Japan, Hong Kong, China, Taiwan and others. Valdes is joined by industry professionals like John Haremza, Mickey Dillon, and Dean Nunneley. This roll call of talent and proven successes has created a powerful atmosphere. Each has experience of over 10 years, mostly with Rexall Showcase International and they are excited about the long term potential of Waiora. Haremza, the top income earner and master distributor, believes Waiora will be a billion dollar company within five years and excited to work with Valdes. Their team just completed a two-day intensive training conference. This event, held in Orlando, Florida, was designed to gather the founding members and the future leadership of the company. Rarely does this industry see a company see 1000% growth, be debt free and profitable within their first two years. For professionals in this industry, Waiora is a opportunity you'll definitely want to consider. NCD is one of the most important nutritional supplements a person could take. To learn more about NCD and Waiora, contact Valdes and her team. Their knowledge and experience make her the winning team of Waiora.
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Donna Valdes is an author, mentor and trainer of direct sales and network marketing for over 11 years. She currently resides in Largo, FL with her family and is dedicated to helping others achieve success, one person at a time. She can be reached 888-658-8778.
Copywright, TeamValco 2006******************************************************** Donna Valdes is a "self-retired" corporate executive. She is an author, mentor and coach for the homebased business, network marketing industry, and teaches thousands around the world how to work from home successfully. Her, her husband and two young children live in Largo, Florida. You can learn more about Donna Valdes at http://www.donnavaldes.com

Testimony on Ritalin and Zeolite

Thu, 16 Nov 2007 01:27:00 GMT

posted by DetoxZeolite
ADD/HYPERACTIVITY

HYPERACTIVITY, ACNE
Kathy Reichenbach (writing about her grandson, Braden)
MichiganMy grandson, age 16, has had a behaviour problem. His school teacher said, “I don’t want him in my class until he is medicated.” My daughter put him on Ritalin. We prayed that something natural would take the place of it.

We know that a lot of these disorders are caused by heavy metals…. We know God answers prayer. A few weekends ago, he came to stay with me. We gave him 10 drops of liquid zeolite [cellular zeolite] starting Friday night, at 6 PM. We started giving him 10 drops four times a day. He calmed right out and didn’t take his Ritalin over the weekend, as it caused him to have side effects he didn’t like.

…My daughter, Angela, asked me, “What did you do to my son? He’s in his room multi-tasking.” He was fixing his room up. He picked up all his clothes, and was organizing his room. He had never done that.

He had final exams on Monday, four days after we started him on the liquid zeolite. He had to ace his German exam in order to get a passing grade, as he was failing German. Angela asked me what to do. (He had been off the Ritalin all weekend and had taken the liquid zeolite instead.) I said, “Because of the differences we’ve seen in the three days we’ve had him, I’d send him to school without the medication. But that’s your call.”

He went to school without the medication. He called me in the afternoon and said, “Grammy-cat, I aced all my exams.”

…. He got straight A’s on his report card without the medication. He stayed off his Ritalin after one weekend on the liquid zeolite. Angela has not gotten one call from the teachers saying that he had forgotten to turn in the homework that he had done. Before, calls from the teachers were frequent. I asked Braden to explain how his head feels. He said, “I don’t have any more noises in my head. Before when I would try and concentrate, I couldn’t concentrate on what I needed to do, there were so many noises. Now I can concentrate.” … It [the Ritalin] gave him a burning stomach and a headache, and that’s how he had to go to school every day. He’d feel like a zombie, and still had the noises in his head.… Braden said, “I’d do anything not to have this burning stomach and headache.”
This was a month and a half ago. I’m now seeing a very calm boy. He’s not so antsy. He would constantly thump his feet when he would sit. He’s not doing that now. And he’s not constantly popping his fingers.

He now has friends at school. Before nobody wanted to be around him because he was so hyper…. It’s his behaviour that is attracting him to the other kids. He’s so happy to be invited to birthday parties and other activities.

He said he’d like to bring his friends to meet me at my house. My daughter said their relationship is so much better now because they can talk to each other now. Before it was a constant fight because she’d try to get Braden to do things, and he couldn’t put it together how to get it done.
He’d come here and say, “It’s just not fun at home.... We fight and argue, and mom doesn’t understand.”
The last time he came, he said, “Things are so much better at home.”
.... Braden is 170 pounds. His acne is totally gone….

He drinks four 16-oz bottles of water a day. We have not put him back on the Ritalin. He is much happier now.

Courtesy of :http://www.zeoliteshealth.com/testimonials_2.html

TheZeoCenter.com
MyWaiora.com
Joseph Lowe