The debate continues incessantly on Ormes, and we all are witnessing everyday more the proliferation of enthusiasts and small producers of white powder gold. Some academicians and skeptics think that this kind of matter, which has been discovered the first time by David Hudson, is a pure chemical matter, with nothing particularly important from a physical and biological point of view. Fortunately, the modern advances of science and technology in the field of nanotech, physics and quantum chemistry, seem to come in aid of this new state of matter. It’s also worth noting a trend change by many physicians and biologists, as well as some very enlightened pharmacologists, who welcome the bioactivity of the m-state elements.
One thing is certain, however. Whether we can not define alchemy the procedures that underlie the production of these monatomic elements, we even cannot deny the great truth in behind of the exotic state in which these elements are found.
Personally, I thought myself for a long time that the result of research of Hudson was the result of a misinterpretation.
After several years of conviction, foolishly skeptical and influenced by academic education, I realized, almost caught by a kind of deep insight, that m-state was more than just chemistry.
Perhaps, it was necessary to deepen what D. Hudson studied at a superficial level (partly because of the lack of specific expertise and sophisticated tools), and then enter in a more accurate domain, considering various options. Aprioristic denial is for skeptics and stupid. The study, the research, testing and reproducibility, belong to men of science, to seekers of truth, whom don’t have to defend an academic chair (in addition to their own arrogance). Fortunately, humans evolved from ape to the Homo Sapiens.
So, we decided was necessary to invest heavily in the creation of a department, in Chymia Laboratorium SA, equipped to perform careful researches on the nature and structure of the m-state elements. From this, we also derived the necessity to establish a pool of engineers to translate the collected data, in a pilot process that would ensure the reproducibility of the experience on industrial scale and then create a repeatable standard for the production of a new and totally innovative class of m-state remedies in pharmaceutical grade.
Monoatomic elements. Is it only a problem of ‘energy’?
The process that we will describe is divided into a series of steps, thoroughly standardized and always repeatable, which are the result of a series of discoveries in the atomic constitution of the m-state orbital. We'll talk one day of this atomic constitution, a topic that was faced several times by different authors, but always without a physical-mathematical foundation as a support, and often without the concrete evidence validated in the laboratory.
There are in fact some very interesting quantum hypotheses, which stimulate research in the right direction. Today, thanks to the technological resources available, can be settled many issues. Until recently it was stated easily that the m-state wasn’t possible to detect by common instrumental analysis. For instrumental analysis was intended chromatography and mass spectrometry only.
Well, this is not strictly true. Or, you cannot detect elements such as m-state, but it is true that on the basis of a comparative analysis it seems to change something in the transition from ordinary matter to the m-state. I mention in this regard, some aspects that shouldn’t be overlooked. I state further that in these circumstances I will not speak for our remedies based on m-state elements or better Ormes obtained by our innovative hi-end process. But I'm leaving out by a standard product, the classic white Mg-Ca based powder precipitated by acid-base reaction. This is to avoid too much confusion.
- We now have really sophisticated tools available to elemental analysis, like ICP-MS, sequential WDXRF Spectrometers, NAA, OC / EC, PIXE, XAFS. We know also the exact list of chemical elements that D. Hudson remarked to be in monatomic state in the results of his experiments. Now, it is sufficient to characterize these elements (such as simple chemical elements) in the starting raw material and in the final result, i.e., the white powder precipitated at the right pH gradient that you know well. Notice I talked of “simple chemical elements and not m-state, theoretically undetectable. The appearance of certain elements or less after the reaction, not existing in the starting raw material, is a real sign of change. Whether you have used analytical-grade acids and bases, the change in traces of detected elements, has not been caused by your reagents and then you have "added elements" which the nature must be investigate, as well as the causes of their appearance. This is already a sign you have something m-state in your compound.
- What makes commonly invisible the m-state elements to elemental analysis systems? Very simple. The cause is in their spin variations, this is well known. Why? Because their spin is faster than normal in common elements and is inverted in z-direction. We will deepen the argument someday, but what concerns us now is to understand what happens during a common elemental analysis. Then, we consider the simplest method: ICP-MS. Inductively Coupled Plasma (ICP) analytical techniques can quantitatively measure the elemental content of a material from the ppt to the wt% range (parts per trillion… very different from what commonly appears in Ormus products analysis, where you have ppm or ppb). The only elements which cannot be measured by ICP methods are C, H, O, N and the halogens. Solid samples are dissolved or digested in a liquid, usually an acidic aqueous solution. The sample solution is then sprayed into the core of and inductively coupled argon plasma, which can reach temperatures of approximately 8000°C. At such high temperature, all analyte species are atomized, ionized and thermally excited, and they can then be detected and quantified with either an emission spectrometer (OES) or a mass spectrometer (MS).
- ICP-OES measures the light emitted at element-specific characteristic wavelengths from thermally excited analyte ions. This light emitted is separated and measured in a spectrometer, yielding an intensity measurement that can be converted to an elemental concentration by comparison with calibration standards.
- ICP-MS measures the masses of the element ions generated by the high temperature argon plasma. The ions created in the plasma are separated by their mass to charge ratios, enabling the identification and quantitation of unknown materials. ICP-MS offers extremely high sensitivity (i.e. low detection limits) for a wide range of elements.
Modified atoms, where spin is faster than normal and inverted, are exotic matter, and this kind of matter can’t be directly detected whit a simple elemental analysis system or common MS.
M-state exist because the atoms’ nuclei are in a superdeformed condition, a totally different state of matter that can be detected only by more sophisticated technology. Imagine a real object (the common chemical element) and its mirror image (the same item in another state, or exotic). Exotic matter exists and is really recognized by mainstream science. It can be characterized but NOT by common elemental analysis systems and/or MS. We have worked for years in this direction and now we can meet the challenge. Moreover, there is another aspect, namely the fact we’ve mentioned above, that is the absence of several elements such as In, Ir, Os in starting matter that appears detectable in the final product of the reaction. So the real reason for this lies at the atomic level, in real transmutation of certain energetic/orbital conditions.
ORMEs, Ormus, m-state, white powder gold. Only ‘marketing’ or true different matters?
It’s really interesting notice that even in “Ormus alchemy” environments, when you show how it works and support the veracity of phenomena in scientific terms, lot of opponents sprout. It seems contradictory but happens. Perhaps they fear that their products without Ormes in bioactive and subtle interacting quantities are exposed? I do not want to go further in this dispute, which frankly is not very interesting. Everyone is free to sell his own product with his brand and his marketing. The consumer will be the judge, and lab validations will give the latest word on the toxicity or otherwise of single remedies.
Often, marketing operations, even when driven by smart people tend to produce certain confusion, creating neologisms or differentiation in product typologies that after all are proven to be the same thing. Running into a site that sells Ormus, during a recent trip around the network, I noticed a fairly common mistake, or the tendency to consider white powder gold, ormus and m-state elements, as three different things. All this is done in the simple purpose of multiply the items in the products catalog, but as it can be done by different color in the same car model. It is very curious that those who often boast of graphics and catchy phrases, are often less aware of the topics they speaks.
The reasons given to support this differentiation are the most fun, even when apparently “well dressed”.
But beyond the aspects of SEO adv, which require the use of keywords appearing within the text in order to maximize the indexing of the site, what is important is that things should be otherwise called by their names. I means that when we speak of Ormus, we speak of products based on m-state elements, which may be in the solid form (white powder gold), or liquid form preparations based on Orbitally Rearranged Monoatomic Elements (ORMEs), that are the ultimate fine matter in monoatomic state (m-state).
Words have their weight. They resonate within us and therefore all our sentences, words and expressions, have a specific resonance frequency in our being the most subtle. Truth should come first. Considering and claim about m-state metals as single pure products placed in a bottle is a big mistake. The monoatomic state is isolable exclusively encapsulated in an ionic solution or a solid support (salts of Mg, Ca, Na), and never as a single element such as the common element that it represent. Monoatomic Ruthenium (mRu) is not the metallic Ru solid at 298 K. Moreover, if we consider the solid support, then not all of Mg, Ca, and Na salts are suitable for a bioavailable transport in the human body.
The monatomic state is an energy/matter identity, a sort of hybrid in which matter and energy remain at high level of atomic quantization. At this level you enter a completely new domain, which requires a leap over the hurdle of academic science.
Indeed, I am the first to say that many of commercial Ormus products, today on the market, are qualitatively excellent. But is more honest do not accuse FDA because of not official approvals and enrolling in HPUS for this new class of supplements. No conspiracy out of there, believe me. The cause leads in dullness of some academic scientists, but also in the hazardous fantasies or deep pseudo-science mistakes of some supporters of the Ormus world. Self-criticism on both sides should be a sign of intellectual and scientific honesty.
I do not deny that there is some resistance to adopt these methods and turn them into of common use. The interests that underlie the pharmaceutical world are heavy, and the m-state matter could be the solution to many problems now largely unresolved. The same is true for applications in the field of agriculture or energy production. It is clear that much money hinges on these things. But I tend do not see an agenda in everything, in every human decision, if not in what is worse.
Rather than words as "essence", “spirit”, and so on…(I like them in any case), terms too much generalist that says everything and says nothing, I would speak of "particular state of matter", or better "exotic mirroring of specified elements". At this level, we should put some order in the interpretations that until now have been given to these elements. Especially in the recent times, a series of inconsistent theories have been formulated to readjust the pitch after certain statements from the Academic skepticism, near to many other interesting and certainly courageous.
The term given by David Hudson is clear: Orbitally Rearranged Monoatomic Elements (ORMEs). They are therefore real chemical elements, belonging to the periodic table, but in a different atomic and quantum state, where orbital is ‘rearranged’ in some way to restitute a totally new quantum-chemical identity. That’s make the REAL difference. The same term "aetheric essence" is bitterly wildcat if token alone. We can't fight academic skepticism by "fantasy" concepts. For this reason, everything claimed must be always contextualized and supported by real proof. Obviously, under conditions of common dialogue, outside the canons of science, and in a perspective in which the synthesis must be obtained to give meaning to things, certain terms doesn’t clash.
A correct identification of the concept of ORMEs, and therefore their proper characterization, involved all of us at Chymia for some years, and many important resources have been invested, both in capitals and human terms. Among those I wish to thank here - before proceeding with the even though partial description of our process for obtaining Ormes - our main Funder. For reasons of secrecy, I will not name him but I want share he is also my undisputed Mentor.
I can ensure that it's possible to isolate individual m-state elements in the form of quantum liquids, room-temperature superconductors, absolutely non-toxic and heavy metals free. They become so real bioactive ingredients, in an exotic and perfectly interacting form, able to restructure on both biological and subtle levels. We have the technology to do this and ensure repeatability of the experiment.
The ORMEs preparation process by Chymia Laboratorium SA.
In search of true m-state elements
There are over 560 different sources for ORMEs and m-state from the three kingdoms of Nature. The main thing is to know how assessing the toxicological impact and once done, to know how eliminate such toxicity for the benefit of a easier absorption and consequent metabolizing by the body. The real key lead in the ability to extract natural ORMEs anchoring them the right vehicle, or chemical matrix, just as the active ingredient in a drug is well conveyed by the appropriate excipient.
The Ormus remedies behave like any drug or any natural remedy (including spagyrics). Once they reached the body, the biochemistry causes them divide into a number of two or three metabolites. These metabolites are:
- partly absorbed, going to impact on the target for which have been studied (as an active ingredient, ie the m-state elements);
- partly expelled with the feces (as an excipients, or carrier molecules).
However, there is a big difference between conventional drugs (allopathic) and natural remedies that has been developed from spagyric and/or homeopathic concepts. In the second case, the action of the potentiated active ingredient involves the totality of human being, in a gradient of holistic levels that are stimulated in the totality of the person (body - mind - soul). Ormus act at the same level, and often even more penetrating, if designed in the proper way.
It’s necessary point out that the majority of ORMEs based products today on the market, are 95% composed of Mg(OH)2, CaOH and NaOH crystals, and only ppm/ppb traces of presumed m-state, usually claimed as periodic elements. From a study of superdeformed nuclei characterization we performed in our laboratories, on a range of over 100 different samples produced by various companies and commonly made in private, only 5% revealed a real presence in the m-state elements, although in quantities not particularly significant.
Same, the simple spin analysis can be conducted for reveal m-state element presence. The study and characterization of the electron spin (z-direction component) can be carried out instrumentally, using a field emission microscope equipped with a 90° sector type spin rotator and retarding spin polarization analyzer. By this instrument only, you can really detect the right behavior of m-state spin vs. any other methods, more theoretical and subjective than not scientific, while superdeformation characterization can help you in understand if you’re or not in presence of relevant m-state matter. The z-direction spin analysis is carried out in two different steps:
- Elemental analysis of all presumed m-state elements according to Hudson’s list, by ICP-MS, quadrupole MS and Mossbauer.
- Preparation of a purified acid solution of the Ormus powder and sputtering onto a ceramic support as nanodeposition.
- The so called m-state elements are extracted with a particular technique and submitted to field emission analysis, with the instrument described above, for characterization of m-state elements.
Though everything has been accurately conducted, then you should find in this white powder twenty-one different TRUE m-state elements. That are, the twelve listed by Hudson, plus six others with special features. The latter ones can vary in reason of the source or raw matter, according an interchangeable list of twenty but always combined in a result of six. Note that the white powder considered as ‘monoatomic gold’, and often made from Dead Sea salt or other mineral deposits according Hudson’s method, should contain at least the following true m-state elements, we give here with our new notation for differentiate them from common periodic elements (m in apex stand for m-state): mCo, mNi, mCu, mRu, mRh, mPd, mAg, mOs, mIr, mPt, mAu, mHg.
In almost all the samples that we analyzed, the presence of these metals (in the elemental state), is pretty exceeding the threshold of toxicity, while the frequency response of the m-state elements (the condensate superdeformed status, characterizing their presence in a positive bioactive level) was extremely low or even absent!
Why is this? Because the all the common methods based on acid/base reaction and pH correction are insufficient to separate all the m-state in solution, as well as to stabilize them in a biologically active form. For this reason we decided to design and build a highly innovative method, assuring a non-toxic, heavy metal free result, where the presence of Ca, Mg and Na is in ionic form, and where a more high content in biologically active non-toxic ORMEs is guaranteed.
Thus, the preparation process is therefore absolutely essential, in order to obtain a perfect remedy with a relevant and true impact at any level of human being.
Toward a new sustainable ORMEs class
GMP stands for Good Manufacturing Practice, as well as TQM stands for Total Quality Management. The rules governing medicinal products in the European Union, Switzerland, USA, Australia, etc. are a series of guidance for the interpretation of the principles and guidelines of good manufacturing practices for medicinal products for human and veterinary use.
All this laid down in specific methodologies certified by specific authorities in the singular Countries (i.e. FDA in USA, Swiss Medic in Switzerland, EMEA in EU). These rules involve typically remedies enrolled in the various pharmacopoeias in force in various countries (i.e.: Homeopathic Pharmacopoeia of U.S. as HPUS, Pharmacopoeia Helvetica as Ph. Helv., Homöopathische Arzneibuch as HAB 2011, etc.). In these pharmacopoeias are described methods of production for various remedies and analysis protocols. By the way, GMP protocols are similar in those Countries where regulation has been transposed to a common level.
Despite Ormus are not covered in various pharmacopoeias of single Countries, as well as in the GMP worldwide regulation, we consider their preparation under the same rules of medicinals manufacturing. This means we accomplish the pipeline process using GMP compliant technologies, clean rooms and certified filling lines. The same in their pharmaceutical form, that is potentized liquid and micronized solid. This gives our products a single standard that other competitors don't currently apply (although some commercial products are anyway excellent, I can confirm). Obviously, this put Chymia in a new vision, both in terms of invested capitals and specialized resources. What we want do is to emerge with a leading product, truly innovative and with sure penetration in the international context, included any possible future clinical trials philosophy.
Among the various questions from we started, at the time to design the process that would allow the total separation of true m-state elements in the right solution for simple and rapid absorption, were:
- the choice of the starting ore, with an excellent concentration in natural m-state elements;
- the bioavailability enhancement of the future active ingredient obtained and purified;
- the stability of the final product in order to avoid deterioration, spin orientation decay caused by magnetic fields and high frequencies, or the displacement of the m-state spin in ordinary spin.
- The starting ore or starting raw material.
The choice of the exact starting mine is never easy, considering that the list of m-state elements found in nature is widespread and never complete for each source. So it may happen that in a mineral or a vegetable, we find a score of m-state elements which doesn’t appear (or only partially appears) in another different or similar source.
After the profiling of over 560 different sources of m-state elements, in the three Kingdoms of Nature, we chosen four different possible bodies capable to provide an appropriate range of true m-state elements in stable form and directly extractable. One for each possible application relative to the classes of product, in pharmaceutical form. That is, Q-Ormes (human and veterinary), m-Unitaries (human and veterinary), m-Ternaries (human and veterinary), FarmeX (gardening and farming).
Alumino silicates from volcanic deposits
Hydrated sodium calcium aluminosilicate is silica clay mined principally in Utah and sold with the registered name of Azomite® that came from ancient volcanic eruptions that deposited ash in a nearby lake bed. The area later over time was submerged under the ocean and had hundreds of rivers flowing into it, depositing even more ORMUS-rich minerals. Volcanoes, ocean water, and river water are high sources of m-state elements. Oceans and rivers are not to be considered a good raw matter, because of recent pollution by radiations and chemicals that make them as unworkable sources according toxicological safety issue. These kinds of minerals are a very good source of high m-state elements found nowhere else in the world. In a typical chemical assay, Azomite® contains more than 70 trace minerals which include many rare earth elements as lanthanides. Many of these elements have been depleted from soils worldwide. In animals, Azomite® has been shown in scientific studies to bind some mycotoxins typically found in animal feed as well as improving Average Daily Gain (ADG), Feed Conversion Ratio (FCR), and reducing mortality rates even in the absence of any mycotoxins. There is speculation that the presence of approximately 70 trace minerals may be the reason for these results, and may improve the health of animals that ingest the product.
The silica clay we use as starting raw matter for the extraction of ORMEs is all natural with no added stabilizers and/or additives, and directly purchased in bulk by the European distributor of AZOMITE Mineral Products, Inc. (USA), Behn Meyer Europe GmbH of Hamburg (Germany).
Especially used for FarmeX production.
[AZOMITE® is a Federally RegisteredTrademarkowned by Azome Utah Mining Co., Inc. and is used byChymia Laboratorium SA exclusively for informational and non-commercial purposes only].
French and Italian Red Clay
Far removed from prominent view, exists an age old substance in nature, known as calcium montmorillonite clay, also knew in its red variety. There are only a limited number of red clay deposits around the world. The first site was discovered in Montmorillon, France in the 1800's, hence the name, Montmorillonite. For centuries Native American healers used it internally and externally in the treatment of a variety of illnesses. In years past sailing vessels departing from France were known to store clay on board for the treatment of dysentery as well as other ailments. Animals, domestic and wild alike, instinctually drawn to clay deposits have been observed licking the clay as part of their everyday diet, and rolling in it to obtain relief from injuries.
The red clay variety is reported to contain no less than 67 trace minerals, 72 in the Italian ore. This impressive assortment of minerals includes calcium, iron, magnesium, potassium, manganese, and silica as well as trace elements those appearing as ORMEs (also in organic form) and in relevant quantities. The mineral content being extremely high sets the stage for replenishing dietary deficiencies. Today more than ever before, diets are lacking essential trace minerals and micronutrients. Without the basic minerals, life cannot exist; without trace minerals, major deficiencies may develop. Lack of either will make it impossible for the body to maintain good health and function properly. In clay the minerals occur in natural proportion to one another encouraging their absorption in the intestinal tract. Natural calcium montmorillonite restores minerals in the tissues where they are needed. Furthermore, Ormus minerals are the carriers of the electrical potential in the cells which enable the hormones, vitamins, and enzymes to function properly.
Especially used for Q-ORMEs production.
French Lava Rocks form Auvergne
Volcanic rock (often shortened to volcanics in scientific contexts) is a rock formed from magma erupted from a volcano. In other words, it is an igneous rock of volcanic origin. Like all rock types, the concept of volcanic rock is artificial, and in nature volcanic rocks grade into hypabyssal and metamorphic rocks and constitute an important element of some sediments and sedimentary rocks. For these reasons, in geology, volcanics and shallow hypabyssal rocks are not always treated as distinct. In the context of Precambrian shield geology, the term volcanic rock is applied to what are strictly metavolcanic rocks. Volcanic rocks are among the most common rock types on Earth's surface, particularly in the oceans. On land, they are very common at plate boundaries and in flood basalt provinces.
Most volcanic rocks share a number of common minerals. Differentiation of volcanic rocks tends to increase the silica (SiO2) content mainly by fractional crystallization. Thus, more evolved volcanic rocks tend to be richer in minerals with a higher amount if silica such as phyllo- and tectosilicates including the feldspars, quartz polymorphs and muscovite. While still dominated by silicates, more primitive volcanic rocks have mineral assemblages with less silica, such as olivine and the pyroxenes. Bowen's reaction series correctly predicts the order of formation of the most common minerals in volcanic rocks.
Occasionally, magma may pick up crystals that crystallized from another magma; these crystals are called xenocrysts. Diamonds found in kimberlites are rare but well-known xenocrysts; the kimberlites do not create the diamonds, but pick them up and transport them to the surface of the Earth. Most modern petrologists classify igneous rocks including volcanic rocks by their chemistry when dealing with their origin. The fact that different mineralogies and textures may be developed from the same initial magmas has led petrologists to rely heavily on chemistry to look at a volcanic rock's origin.
The chemistry of volcanic rocks is dependent on two things: the initial composition of the primary magma and the subsequent differentiation. Differentiation of most volcanic rocks tends to increase the silica (SiO2) content, mainly by crystal fractionation. The initial composition of most volcanic rocks is basaltic, albeit small differences in initial compositions may result in multiple differentiation series. The most common of these series are tholeiitic, calc-alkaline, and alkaline.
The lava is a fascinating chemical universe, in which fire fixed a significant amount of Ormes, over 40 different true m-state elements in stable form.
Especially used for m-Ternaries production.
It is pointless to talk extensively about a metal that everyone knows and that for its physical-chemical properties is regarded since millennia as the King of metals. This valuable chemical element with the symbol Au, represents definitively the indispensable source for production of g-Ormes and ultrapure m-state unitaries. There are very few true gold ores, besides native gold, because it forms a major part of only a few rare minerals, it is found as little more than a trace in a few others or it is alloyed to a small extent with other metals such as silver. A few of the minerals that bear gold in their respective formulas are in a subclass of sulfides called the tellurides. The element Au seems to have an affinity for tellurium and this is one of the only elements that gold can bond with easily. For this reason in true g-Ormes you’ll find always a relevant amount in mTe. In fact only a few rare tellurides are found without gold. A few of the tellurides are nagyagite, calaverite, sylvanite and krennerite. These are all minor ores of gold and their contributions to the supply of gold pales next to native gold's own contribution. Occasionally these minerals are associated with native gold.
Especially used for m-Unitaries production.
(end Part I)