It appears that the key to great physical longevity is the discovery of a method for effecting the repair of DNA. Accumulated damage to the DNA has been called one of the major factors in aging. It is also generally considered to be a major factor in cancer, aids and other degenerative diseases. David Hudson in his lectures and workshops claims that the ORMUS materials have reversed the progress of cancer and other diseases. Hudson suggests that this reversal is the result of the repair of DNA which is facilitated by the ORMUS elements. Here is a quote on this subject from David Hudson's Portland, Oregon lecture:
"They claimed that it perfects the cells of the body. Well I can show you tomorrow Bristol-Myers-Squib research that shows that this material inter-reacts with DNA, correcting the DNA. All the carcinogenic damage, all the radiation damage, all is corrected from these elements in the presence of the cell. They don't chemically inter-react with it, they just correct the DNA.
This is not an anti-anything. This is not anti-aids. This is not anti-cancer. This is pro-life. It literally is the spirit. The material is not here to cure aids. The material is not here to cure cancer. The material is here to perfect our bodies. It makes our bodies be in the state they are supposed to be in. It is our own immune system that fights and cures the disease. If you can correct your DNA at every cell in your body. If you can correct the damage that's been done that brought about the cancer, if you can correct the damage that has been brought about by the virus; the aids you literally will become a perfected being. You will return back to the original healthy state you were meant to be in."
Here is another quote on this subject from Hudson's Dallas lecture:
"Now what does it do in the body? It literally corrects the DNA, by a process the equivalent of a denaturing solution, the DNA relaxes and recombines corrected. So all diseases that originate with a problem with the DNA can be corrected, but your reason for taking it cannot be to correct a disease. Your reason for taking it has to be a philosophical reason. It has to be to enlighten and to raise the nature of mankind. If in doing that, it happens to cure the diseases, so be it.
And I just saw this. Dan Winter does such a good job of depicting it that I said, oh hell, I'll just use his slides. It just so happens that Dan Winter said that the nucleus or the DNA interacts with this frequency. So people in music and all this that play all this beautiful music, they say it calms the soul, it does all these things, they say, "Dave, would music effect the DNA itself?" I don't believe so because, I think, that what you're trying to effect is in fact a null, and that frequency that you're trying to generate is in fact a frequency so short that even our nuclear physicists can't produce the Planck frequency. But that frequency in fact is where everything is and that frequency just happens to interact with the DNA in the cell. It is the God-Force or the Creative Vibration or the energy that is everywhere timeless in the universe and that's what the electro-magnetic null produces. So what frequency is it? It's not important. It's two waves equal and opposite, that's what's important. (audience question) It's actually Dan Winter's book, it's a big thick book, but I don't remember the title of it. It's Dan Winter's book and that's what it's in. Anyway, next slide.
And here he says, he's showing the cell again, the inter-reaction of the zero point energy which he shows depicted as the center or literally that the vibrations actually go to null, to nothing and that's the center. And that's the frequency inter-reaction of the DNA. That's one way of picturing it and so I'm using his slide, but that happens to be the frequency that does interact with the DNA, and his terminology here is, lightning-spun up-primal soup- all lightning is unipolar because of the consistent orgone electro-negative. Well he's talking about this as orgone energy. That I don't know if I ascribe to, I don't know if I like his terminology here, but his concept of the electro-magnetic zero point is accurate. I'm not telling you that I believe everything that Dan Winter writes, I'm telling you that this particular part of it is accurate. Next slide. Okay, next slide."
(An explanation of what the ORMUS elements are and some methods for obtaining them is available on the web at:
http://www.subtleenergies.com/ormus/ormus/ormus.htm)
The immune system is also degraded by DNA damage. We suspect that any disease condition which is related to either the immune system or damaged DNA might benefit from ingestion of the ORMUS materials.
A recent Associated Press story talks about the discovery of an "aging gene" named WRN which:
"appears to play a vital role in how DNA repairs itself and reproduces, long suspected as keys to aging". . . "Normal WRN appears to govern the production of vital enzymes called helicases."
"DNA carries the body's genetic blueprint, in double-helix strands coiled inside every cell. Whenever a cell reproduces, the DNA strands first must uncoil so they can be copied accurately for the new cell. Likewise, whenever the body needs to repair a cellular defect, the DNA must unwind so repair enzymes can snip off the defective piece. Helicases make DNA unwind."
"If WRN is mutated, presumably the helicases aren't uncoiling DNA properly - so cells aren't reproducing to replace dying ones or DNA damage is not being repaired"
Three recent papers suggest that the platinum group elements can assist in this process of DNA repair:
Platinum Metals Review
1990, Volume 34, Number 4
Biophysical Studies of the Modification of DNA by Antitumour Platinum Coordination Complexes
"The modification of DNA by cisplatin has been examined. Anti-tumour active Pt compounds induce in DNA, at low levels of binding, local conformational alterations which have the character of non-denaturing distortions. These changes in DNA occur due to formation of inter-strand cause links..." p. 235
Scientific American
May 1995
David Paterson
"The researchers examined the electrical properties of short lengths of double-helix DNA in which there was a ruthenium atom at each end of one of the strands. Meade and Kayyemestimated from earlier studies that a short single strand of DNA ought to conduct up to 100 electrons a second. Imagine their astonishment when they measured the rate of flow along the ruthenium-doped double helix: the current was up by a factor of more than 10,000 times-over a million electrons a second. It was as if the double helix was behaving like a piece of molecular wire."
"For some time, chemists have suspected that the double helix might create a highly conductive path along the axis of the molecule, a route that does not exist in the single strand. Here was confirmation of this idea." pp. 33-34
Matti Pitkanen, a theoretical quantum physicist in Finland, wrote the following about the third article which appeared in Science magazine:
In the newest Science, vol. 275, 7. March 1997 there was a very interesting article about the work of Barton and her group. Barton et al have done several experiments between 1993-1997 related to the conductivity properties of DNA double helix. The conclusion of Barton et al is that DNA double helix has the ability to do chemistry at distance: "A DNA molecule with a chemical group artificially tethered to one end appears to mediate a chemical change far down the helix, causing a patch of damaged DNA to be mended.".
DNA as conducting wire instead of insulator
What seems to occur is flow of electron current along DNA with very small resistance. Typically the experiments involve electron donator and acceptor separated by a long distance along DNA. When acceptor is radiated it goes to excited state and an electron current flows from donator to acceptor as a consequence. Standard wisdom tells that this should not be possible. The current should flow by quantum tunneling between adjacent building units of DNA and it should diminish exponentially with distance. For proteins this is known to be the case. In experiments however no distance dependence was observed.
There exist a theory which assumes that the current could flow along the interior of double DNA, that is the region between the bases of strand and complementary strand. The electron would be delocalized in bases rings these rings would form a stack along DNA. The current would flow by tunneling also now but the tunneling probability would be so large that distance dependence would be weak. The critics of Barton argue that this model cannot explain all the experiments of Barton and that the model is not in accordance with basic organic chemistry and biology: ordinary sun light should have rather drastic effects on us. Barton admits that they do not understand the mechanism.
TGD-based explanation in terms of exotic atom concept
TGD suggests a possible explanation of phenomenon in terms of closely related concepts of exotic atom and charged wormhole. The concept of exotic atom in turn relies on the concept of many sheeted spacetime. Exotic atom is formed when one or more outer valence electrons of ordinary atom are dropped from atomic spacetime sheet to a 'larger' spacetime sheet, now spacetime sheet with a form of DNA helix. As a consequence, charged wormholes feeding the em gauge flux to the larger spacetime sheet are also generated. Electrons in larger spacetimesheet could be delocalized and this could lead to a smaller ground state energy. What is important is that the electrons on the larger spacetime sheet move effectively in empty spacetime and therefore electric current can flow freely without resistance.
Charged wormholes could provide also a mechanism of superconductivity: photons are replaced with the excitations of wormhole BE condensate in this mechanism. It is however too early to say whether super conductivity is really in question and even whether this superconductivity mechanism really works.
In the experimental arrangements of Barton typically donors and acceptors of electrons are Rh and Ru atoms. Both have 5s unpaired electron and this electron would drop on the larger spacetime sheet from the atomic spacetime sheet and induce electric current. Some colleagues of Barton did not observe the effect when using organic molecules as donors. A possible explanation is that these molecules are such that their valence electrons cannot drop on lower spacetime sheet (it is not energetically favourable, they could be paired, for instance).
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For exotic atoms, charged wormholes and the related mechanism of super conductivity see my homepage
http://blues.helsinki.fi/~matpitka
Additional references to papers by Dr. Jacqueline Barton can be found on physicist Tony Smith's web page at:
http://www.innerx.net/personal/tsmith/newtech2.html
(Tony Smith goes into additional technical discussion on many of the issues raised in this article.)
From these three papers, it should be clear that the repair of DNA may be linked to the presence of the platinum group elements.
David Hudson claims that he has provided ORMUS materials to various medical doctors who have given them to patients with cancer. According to Hudson, in the great majority of these cases the cancer patients have recovered with indications that the cancer tissue reverted to normal tissue. Hudson reports that the tumors at first appeared to grow because cancer tissue is more dense than normal tissue. Since the cancer was becoming normal tissue, as it became less dense it would expand.
In his Ashland, Oregon lecture Hudson said:
"First of all, if you use the rhodium and iridium, one of the things you can see is that in the first 3 to 4 weeks the tumor actually appears to grow faster. So if you have taken a biopsy, and found that you have a tumor, if you take the rhodium and iridium, in the first 3 to 4 weeks the magnetic resonance imaging will show it's growing faster, which really scares people. They say 'God, that's not what I want'. What you have to understand is, that the dense cancer tissue, when the tissue is converted to healthy tissue, it enlarges in size. And so if the physical tumor is this large (gesture), when it's cured will be this large (gesture). It actually gets larger because it's going to healthy tissue. It's called necrosis in the medical community. Its the opening up of the tumor, okay, and the going to normal. After 60 days you do a biopsy on the tumor and its no longer cancer. Its a benign tumor. The doctors who surgically remove the tumor say 'Gosh, it looks like cancer, looks like it ought to be cancer, it was cancer 60 days ago; its just not cancer now...I don't know what to explain.' Well, that's okay. It takes about a year and a half for all this mass of tumor to dissolve away.
So... if you have a cancer in the brain, if you have a brain tumor, my advice is to stay away from this. And the reason for it is there seems to be a growth. And that's a problem when you have a brain tumor because your brain is encapsulated in a skull, which has a limited amount of room. And so I advise people, you can have surgically implanted a radioactive iridium pellet -which you don't have to have radioactive, you can put the [non-radioactive] iridium and it goes away too, but they make it radioactive so that standard science can accept that this is why its going away; I thought 'That's stupid' when I read that. Anyway then, implant this pellet in the tumor, and the tumor shrinks down to the point that they can surgically remove it, without hurting the brain. Then they actually take the tumor out and they take the pellet out also. Then you can take the material. Okay? But my advice to you is to be careful in dealing with brain tumors, because you do have a space limitation here."
Hudson says that he provided ORMUS materials to the National Institute of Health for in-vitro studies. Here the results were no less stunning but appeared to provide conflicting results. Most of the cancer tissue cultures did not show reversion of the cancer tissue to normal tissue but rather showed that the cancer just became more healthy. Here is an excerpt from Hudson's July/August, 1996 newsletter:
Now to RESEARCH:
The National Institute of Health has performed cancer cell testing. Six kinds of tests were performed on leukemia with no direct intereaction with rhodium. Nine types of non-small cell lung cancer were tested with direct retardation of only one type of cell by the rhodium. That was NCl-H23. There were seven varieties of colon cancer tested with no intereaction with the rhodium. There were six varieties of CNS cancer with no direct intereaction.
There were eight varieties of Irialanoma with one variety referred to as the LOX IMVI, showing a dramatic reduction of growth in the presence of rhodium. The LOX INVI cancer cells are a melanoma form of cancer.
There were six varieties of ovarian cancer, six varieties of renal cancer, two varieties of prostate cancer, eight varieties of breast cancer, none of which showed any direct intereaction with the rhodium. There was MD MID tests performed on Delta and also on the Range showing dramatic reduction in cancer activity.
Members should be clear that this was not a study on human patients. It did not measure any reaction with the thymus or other organs in the body. The tests did not measure increases in white blood cells, T-cells, etc. it was simply a test of the direct intereaction of one ORME (rhodium) in a cell culture.
Additional studies were conducted in New York on PC3 independent prostate cancer cells. At two, four and ten micrograms per milliliter the rhodium ORME promoted DNA synthesis (measured by the thymidine incorporation), stimulated cell growth and cell looked better than usual. Thus rhodium ORME is not toxic, but in fact seems to make the cancer cells more vigorous and robust and clearly does not retard PC3 cancer cells.
Similar results occurred with mink lung epithelial cells. Incorporation of tritiated thymidine increased from 7000 cpm to 20,000 cpm.
In PC3 cells, rhodium ORME caused cytokine, mRNA and peptide levels to fall. This correlates with the increased growth rates in these cells, since this cytokine is known to inhibit cell growth. It also is known to increase in inflammatory conditions, therefore it is possible that the decrease in the cytokine caused by the rhodium ORME could reduce inflammation.
At the university of Illinois, the rhodium ORME was tested in cytotoxicity tests using eight different cell lines. None showed toxicity at levels as high as twenty micrograms per milliliter. This shows that rhodium ORME is not toxic. Clearly Rhodium ORME does not act on cancer cells by killing them, but many other mechanisms which are not considered normal in cancer research are now being investigated.
In Summary:
Rhodium ORME is clearly not toxic, even at very high concentration. Thus its anti-cancer action can not be via a cancer cell-killing mechanism.
Its effects on growth of cancer cells is cell type specific. It inhibits growth of liver cancer cell lines and the prostate line H23, but not the growth of other cell types. It actually stimulates the growth of PC3 cells and mink lung epithelial cells.
It inhibits the production of cytokine in PC3 cell and mink lung epithelial cells, which suggests the rhodium ORME may have anti-inflammatory activity.
The implications of this discrepancy need to be examined. If, with exposure to the ORMUS elements, cancer cells revert to normal cells in the body but do not do so in the petri dish then there must be some factor, which promotes this reversion, that is present in (or around) the body and that is not present in a petri dish .
A gentleman named Gary, who describes himself as a "kundalini awakened American engineer" wrote the following explanation for his theory about a mechanism for DNA repair in the body:
"Regarding Hudson's negative results with in-vitro cancer cultures. Cell cultures do not behave the same as their in-vivo equivalents, for processes that involve kundalini. Cell cultures contain pranic energy, but they lack nadis, and kundalini. As kundalini generally oversees and directs the use of ORMEs, this means ORMEsactions in vitro will be substantially impaired, and much less effective, than in vivo.
Some have asked incredulously and sometimes vituperously how DNA could possibly be repaired and restored to its original sequence by *anything*, once damaged. I have listened to several such exchanges. Some apparently believe that, once the DNA is damaged, nothing remains to base a correction on, and hence have difficulty understanding how ORMEs (or anything else) could know *how* to "fix" sequencing damage, once it has occurred (assuming, of course, that both halves of the DNA have been altered).
Each of us has an etheric double, which is the coarsest of the subtle counterparts of our physical body. This and some subplanes of the astral are the level or home of an 'elemental', associated with the innate consciousness of the physical body. This is a separate consciousness, like those I touched on in explaining the nature of consciousness in matter, earlier.
Regardless of the physical damage cellular DNA may sustain, such as by ionizing radiation, phage-induced mutations, etc., the subtle template is always there, and though it may be depleted of vitality, it is not susceptible to these sorts of structural damage. It is around this prescient organizational form that our bodies grew, in genomic expression, once the individualization phase began in later fetal progress. Every molecule **related to organization and structure** has its subtle counterpart, within it. This is the same matrix which has been observed in the "phantom leaf effect", etc., in Kirlian photography.
Kundalini and ORMEs both function, in large part, in 4th dimensional astral levels. The original subtle "backup copy" of the DNA is readily available to them, at the precise place where it is needed, right at the damage site in the errant cell's DNA. The subtle part lies, superimposed 4th dimensionally, right where the physical part is, and there is no problem at all, in seeing where the two don't agree. There are a variety of mechanisms that repair DNA. In some cases, given sufficient ORMEs in the system, kundalini simply uses the ORMEs as a mechanism, like a read/write head so-to-speak, in repairing the damage. ORMEs are used to transfer a resonance from the subtle template, to guide the DNase, polymerase, endonuclease, and other various enzymes in removing and recoding the damaged base sequences. Each of the bases has a distinct vibrational signature, which the enzymes have no trouble at all in recognizing.
In a cell culture, the cell's own subtle template is present, but no kundalini is present as an organizing force, nor overall template, and virtually no organization is present among the cells, so the genotypical expression elements are largely running open loop. How likely is it that ORMEs may effect a cure under these conditions? Not very(!), though they still seem to have some slight beneficial effect. I suggest they shall have better luck with curing cancers when they experiment on lab mice and other living creatures."
In a nutshell, Gary is suggesting that a non-physical template for DNA exists and that where this non-physical DNA template is available to the physical DNA the ORMUS elements can facilitate the repair of the DNA to this healthy template. Let's examine these concepts.
SOURCE LINK: http://www.subtleenergies.com/ormus/tw/dna.htm