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THE PROTOCOL FOR GULF WAR SYNDROME THAT HAS MOST HELPED ME!

Gulf war syndrome is a disease that has been characterized by multiple varied methods of expression. There are several theories of causation and possible mechanisms. This varied expression and possible theories of origin, mixed with long term denial and lack of appropriate action, have resulted in the initial cases spreading unchecked and with the spread, came new bizarre symptoms and expressions of the disease.

Advocates of a bacterial or mycoplasma causation, promoted and still continue to promote, long term Antibiotic therapy and yet, in what must be a paradox to the supported mechanism. Gulf War Veterans often not only relapse, following the long coarse of Antibiotics, but relapse in a resistant amplified version of the same. Usually with worsening symptomology and new dysfunction resulting.

The preliminary data even suggests that a coarse of high dose antibiotics, may not only directly do damage to the patient, but by some method promote greater spread of the disease.

It appears that Gulf War Syndrome whatever the original causation acts by genetic mechanism which may be harbored at a cellular level, whether within the patient’s own cells or within a variety of possible microbial carriers. Damaging agents therefore that, bring about break down of normal human tissue, or even of microbial structures carrying genetic messages for Gulf War Syndrome, will lead to the amplification and increased infectivity of such agent.

Picture for example, a virus that is well encapsulated by the bodies’ cells. The cells may assimilate the virus and place it in a pro viral inactive stage. In a form of self-sacrifice, which ultimately may destroy the housing cell, but would stop the virus from being able to spread at a high rate, and places it more or less into a dormant state. The same can be said for viruses of lower life forms. This encapsulation mechanism allows for greater survival of the organism and allows for less spread amongst members of the same species. When destruction of this encapsulating cell occurs, either by antibiotics or by some form of trauma, such as sunburn or other radiation exposure (for example.) The genetic vectors, being encapsulated by the cell are released to find new hosts, new cellular hosts and new patient hosts.

Mycoplasma-Sporoid Symprotits

Appearance wise mycoplasma may assume a variety of forms having tails or projections on a spherical or donut shape. They can appear in the blood serum, in leukocytes (white blood cells) or on red blood cells looking like little doorknobs which often make the red blood cell appear like a water mine. Mycoplsama is one of the developmental forms of the parasitic endobiont (as most every negative thing is that is seen in the blood.) 

It is a symprotit that contains a surrounding protein substance. Its appearance in the blood happens as fast as you can snap your fingers. For instance, let's say you are viewing a red blood cell in live blood. All of a sudden, poof, a mycoplasma forms on a red blood cell as if it were from nowhere. That's just how it happens. Enderlein calls it an endoboiotic formation that occurs from a quantum biological leap. If the conditions in the terrain (the environment of the blood) is just right, (the pH isn't high enough) the colloids within will jump to the mycoplasma level in the blink of an eye. 

Standard hematology classifies mycoplasma as a free living organism which is a genus of highly pleomorphic bacteria that lack a cell wall and are separated into many species.

Seeing them is another indication that pH is off, oxygenation is low , the immune system is compromised, and there is potential degenerative disease implications. Physical signs could be any of 1000 different things. 

The preceding pages covered some key concepts relative to the rotting mechanism of the body.  The rotting mechanism of the body is the biological equation. The flip side to this is the rusting mechanism, which is a chemical and electrical equation.

As we age and get diseases, we are experiencing the effects of Rot & Rust. It is an interplay of the biological, chemical, and electrical physiology of the human body.

With a firm understanding of this knowledge, the microscope becomes a tool to delve into this interplay at its most basic level - in the blood.  To learn more about pH and Mycoplasma please take the time and take the tour!
Click here to take the how you rot tour!

My Name is George Nadzan, I am a civilian that has been clinically diagnosed at the University of Michigan hospital with Gulf War Syndrome via testing positive for the cell wall deficient bacteria Mycoplasma Fermentans (incognitos strain). It seems that I have one of the more severe cases of gulf war syndrome due to the fact that my symptoms have turned to the destruction of my central nervous system. Over the past 7 years I have spent nearly a quarter of a million dollars in the attempt to treat my symptoms to until now, no avail.  Below is a list of some of the medications that I have taken and I cant even remember them all: Ciprofloxcin, doxycycline, azithromax, chlorenphenicol, tetracycline, lincomyacin, penicillin, trimox, leviquin, floxacin,  Hydroxyzine, Diflucan, Mycelex, ceftin, Biaxin, bactrim, sulfazine, tegratol, neurotonin, Hydrocodine, codine, nulev, cyclobenzaprine, percocet, endocet,  morpine, tigam, prochlorperazine, celebrex, deltazone, prednizone, zytrec, psuedifed, epinephrine,  and about a hundred and fifty thousand dollars worth of immune therapy and genetic  treatments and these are just a handful that I can remember, from over the last 5 years and there are dozens of others I can't Remember. 

Now there is a reason for  me telling you all of this, and it is because none of these drugs have Worked or will work for me  and they have destroyed my body as much if not more then the organism itself. 

When you realize what the power of God can do for you, what it has done for me, and when you learn what is written in the book of life, and not to put God in a box and the way He works, your name too can be written in the book of Life and your health can be restored. If you learn the whole truth about His living word and that our Father wants all His Children to be in Good Health.

(KJV) 3 John Ch. 1 vs. 2-4.    2. Beloved, I wish above all things that thou mayest prosper and be in health, even as thy soul prospereth.3. For I rejoiced greatly, when brethren came and testified of the truth that is in thee, even as thou walkest in the truth. 4 I have no greater joy than to hear that my children walk in truth. This proves that it is God's Will for all believers to be in good health { Health= Gr. 'Sound Doctrine'}. 

Rev. 18:23 And the light of a candle shall shine no more at all in thee; and the voice of the bridegroom ( Christ) and of the bride  ( those with the Baptism of the Holy Spirit) shall be heard no more at all in thee: and the voice of the bridegroom and of the bride shall be heard no more at all in Thee: for thy merchants were the great men of the earth; for by thy "Sorceries 5331" were all nations deceived. 

(now the definition of the Greek word sorceries from the book of strongs numbering is 5331 and its definition is pharmakeia from the word 5332 pharmakeus, or  pharmakon  which means," medication i.e magic, sorcery, witchcraft. from pharmakon: spell giving potion, a druggist ("pharmacist" or poisoner, i.e.)   ( by extence.) a magician:-sorcerer

Now do you see all the medications I listed above? are you getting the point! 

Their sorceries, Their witchcraft. Isn't it time to return to the Lord and His ways or do you want to follow man and mans ways and end up like me almost dead, going numb intermingled with nonstop pain from head to toe. 

 *THE PROTOCOL FOR MYCOPLASMA INFECTION/ALS THAT HAS MOST HELPED ME!

 Dosage for adults as a dietary supplement of Eniva's Ionic minerals.

*IMPORTANT NOTE: Food allergies, a removal of all wheat and gluten related products, all Milk, Cheese and related products and all products containing chocolate, for a minimum of 6 to 8 months may be necessary to allow for the gut to heal and the gut flora and E3live to do its job. I personally have gone almost completely meat free other than occasionally deep-water fish. The reason why GW Vets and Fibro patients crave chocolate is because chocolate has a high magnesium content. What they are actually craving is magnesium. However patients with intestinal permeability tend to be extremely allergic to chocolate. Milk and wheat gluten proteins closely match our own proteins and when an immune response is triggered to go after allergens, histamines and mast cells are released and can attack our own central nervous system. I found immediate relief from a lot of my intestinal symptoms with the use of E3Live algae and good gut flora and Licorice root. Some people however may even be allergic to gut flora if the intestinal damage is severe. Benedryl may be of some use in stopping the release of histamines, mast cells and some of the more severe allergic reactions. Dr. D'Adamo's book "eat right for your type" might be a good start for learning about your diet. See also GWS the histamine connection.

	Eniva's Living Health pro-biotics,  Click here for Eniva's Complete line of Liquid Ionic Minerals and supplements:

Genesis 9:15-17 And I will remember my covenant, which is between me and you and every living creature of all flesh: and the waters shall no more become a flood to destroy all flesh. 16 And the bow shall be in the cloud; and I will look upon it, that I may remember the everlasting covenant between God and every living creature of all flesh that is upon the earth. 17 And God said unto Noah, This is the token of the covenant, which I have established between me and all flesh that is upon the earth.

 

Gulf War Syndrome: some observations

Paul Shattock, Autism Research Unit
University of Sunderland, UK

Our interest in “Gulf War Syndrome” (GWS) was fired, initially, by the coincidence of some of the symptoms we had seen in subjects presenting with GWS and which we had seen in autism and associated disorders. Our hypotheses on GWS are based upon our work with autism and the “Opioid Excess Theory” to which we subscribe. Our work will be explained in terms of autism and then extended to demonstrate that the same principles could be relevant in GWS.

The symptoms of autism are, we believe, the consequence of metabolic abnormalities (Shattock 1991). Normally, proteins are digested in the gut and broken down into amino-acids. During this process, and for a comparatively limited period of time, intermediate compounds, known as peptides, are formed. These peptides, typically of 2 - 8 amino-acids, are usually biologically inert but some are known to have marked biological activity. Thus, various casomorphins (from the milk based protein casein) and gliadinomorphins (from gluten from wheat and some other cereals) will be produced. The activity of these compounds is, as their names would imply, opioid in nature.

Under normal conditions, only a small percentage of these compounds would cross from the lumen of the gut into the blood stream and a small proportion of these would cross the Blood-Brain Barrier (BBB) and enter the Central Nervous System (CNS). Once in the CNS they would result in opioid activity. This could either be the result of the direct opioid activity of the molecule or the fact that the molecule would form a ligand for the enzymes which would normally break down the naturally occurring opioids, such as the endorphins and enkephalins, so that these would persist for much longer than normal. Whatever the source of the opioid activity, these compounds would affect (and usually inhibit) transmission in all of the main neurotransmission systems. Perception; cognition; emotions; mood and even motor activities would be affected by the presence of these compounds.

In particular, the executive control functions would be affected (inhibited) with the result that aggression and difficulties in controlling temper as well as speech would be consequent. Both of these abnormalities are clearly evident in the subjects with GWS with whom we have come into contact. The effects of GWS on bowel function would also seem to confirm that some form of enteropathological effects are present.

Since opioids are intimately involved in the immune system, elevated levels of these compounds would have profound effects on this system and predispose to infections of all sorts. the implementation of a severe active immunisation programme would, under these conditions, have very predictable and deeply unfortunate consequences. We suspect (and have some unpublished evidence to suggest that) some of the symptoms seen in some veterans in the Gulf War could result from lingering disease states caused by a grossly inflated requirement made upon a subject with a compromised immune system.

We have identified a key marker compound (trans-indolyl-3-acryloylglycine, IAG) which is a (the) major component in some 75-80% of people with autism. This compound has no opioid activity itself. We have determined the structure of this compound and feel that it most likely represents the detoxified version of a compound which could have severe but subtle consequences. One of the major actions of this compound would be to render all membranes very permeable. Thus, the gut wall and the BBB would become much more permeable.

This compound is a major component in some 20-25% of the normal, asymptomatic (as far as we know) population. However, it is either the largest or second largest component in each of the (15 so far) subjects reporting GWS we have examined. We do not know the source of the compound but believe that it could be the result of Organo Phosphorous compounds upon the normal metabolic processes. Alternatively it could be there as a normal metabolite in those individuals with a predisposition to these problems.

We see IAG as being indicative or, more likely, involved in the causation of increased permeability of membranes. The active compounds are peptides which are exogenously derived from gluten and casein.

For many years, following advice from a variety of sources or based upon their own observations, parents have been experimenting with diets devoid of gluten and casein in an attempt to ameliorate the symptoms of autism in their children. We are currently conducting a pilot study using such interventions and the preliminary results would appear to be very encouraging and supportive of the results published by Reichelt (1991). For this reason we have suggested to a number of individuals presenting with GWS that they experiment with a diet which is devoid of gluten and casein. The hypothesis is that by doing so, the symptoms would be ameliorated.

No formal study has been performed but it is our very clear impression that those individuals who have experimented in this way, entirely at their own expense, have shown impressive improvements in many diverse ways including speech and aggression control and bowel function.

There are many other interventions which these hypotheses would indicate as being helpful in dealing with the syndrome but, if nothing else, our studies convince us that removal of gluten and casein containing foods is worthy of consideration in cases of GWS.

Reichelt KL,  Knivsberg A-M, Lind G, Nodland M. (1991) “Probable Etiology and Possible Treatment of Childhood Autism” Brain Dysfunction  4. 308-319

Shattock P, Lowdon G. (1991) “Proteins, Peptides and Autism Part II: Implications for the Education and Care of People with Autism” Brain Dysfunction 4. 323-334.

Please note that any decision to try dietary intervention of this type is only recommended with
the support of both a General Practitioner and a state-registered dietitian / nutritionist.

 Access the Gulf War Veteran Resource Pages

 

To learn more on intestinal permeability Click here to read Dr. Leo Galland's M.D. article on intestinal permeability.

*This  information is a collection of minerals and dietary supplements that are believed to be deficient in the body that promote the development of conditions that are unhealthy and take away from a natural healthy state. These statements have not been evaluated by the Food and Drug Administration. These products do not intended to diagnose, treat, cure, or prevent any disease. The information has been compiled from the information provided by those who have been helped from extensive research and experience. The information contained herein is not medical advice and is not intended to replace the advice or attention of health care professionals. Nor is this information intended to act as a "prescription" for treatment. These are ONLY suggestive guidelines for dietary supplements that may supplement the body's nutritional requirements to maintain optimum health. Consider consulting your health care provider before beginning any new dietary supplement program.

 

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