Most of you are familiar with the Dead Sea. For those of you who are
not then please visit my web site and look at the Dead Sea Manna page
Just scroll down the page and click on the Dead Sea Gold link...there
may be something written there that you did not know :-)
There are various forms of the Dead Sea available to us in the U.S.
There is the sea salt, which is sold under various trade names and is
mostly intended for use as a bath salt.
And there is the actual Dead Sea water, which I call brine because of
its nearly saturated state.
There has been mention that the Dead Sea precipitates contain
ORME/ORMUS/M-state. However, there has been great debate whether the
dried sea salts contain the M-state elements or not, and if indeed the
actual Dead Sea water does and indeed if the Dead Sea waters and salts
available to us are actually from or of the Dead Sea at all.
To further complicate matters the Essene said that these elements were
indeed present in those materials as well as the other oceans such as
the Pacific and Atlantic, etc. That these elements could be brought out
as a white powder/slurry and then reduced to metal.
He cited several processes which had been successfully applied to that
end, including some of historical importance which the Essene claimed
remembering having actually performed with King Solomon.
In a sustained effort spanning more than 4 years I have been attempting
to separate fact from myth. I am not going to draw any conclusions for
you and am just going to give this information to you with as much
accuracy as I can.
I have investigated many source materials and have forwarded some of my
findings, including the certified assays and spectroscopic analysis to
Barry Carter who has been spending days sorting the various scans out
and placing them into a format which is being made available to you:
This Series will deal mostly with the Dead Sea as well as with the
common chemicals used by me in their making. I will say up front that I
have also investigated many dry lake beds, ores and mineral materia
from nature and have had comparable results. So, this information and
the methodical thought processes behind the findings apply equally to
the Dry Method precipitates, however, the yield varies tremendously
from one ore to another.
To actually begin this exportation of information to you waiting
information importers I'll begin with telling you that during the years
I have acquired actual Dead Sea water and actual Dead sea salt through
the Ministry of Trade in Tel aviv. So, when I say that this was Dead
Sea water or actual Dead sea salt then you know what it is.
When working with other sources I will list the brand name and form ie,
To begin: I believe that Barry has made all of the Dead Sea Series
available on the same spreadsheet. Please just ignore the others until
you know what they are, please :)
Lets assay the starting material! The name of the sample is in capitol
letters and its description follows it...
DSB06 ................ This is actual Dead sea water analyzed by Group
2C-MS by ICP-MS.
SPADSS ............. This is Spa Brand Dead Sea salt which is
actual Dead sea salt and dissolved into commercial distilled water.
Analysis is as above stated.
MAS106 .................. This is MASADA brand unscented bath salt
which is dissolved into commercial distilled water. Analysis is 2C-MS
as above. This is so commonly available that a lot of my work was done
The FLOW of the Work which is intended to ascertain if there are
any changes to the material follows a logical pattern...The Essene and
David Hudson both agreed that if the ORMEs/M-state is present that
there are several things which tend to cause it to "make metallic
bonds" or form metal. Some of these things are:
Light, specifically deep infrared or higher, like UV and direct
Carbon Monoxide, CO
(nope, that's really NOT a town in Colorado ;-)
Strong EMF, such as microwave, or even electric burner energy.
Elemental sulfur at high heat. (Essene)
This is not a complete list but represents a lot of what I worked with.
As you can see from the brine assays listed above, the ORMEs do not
show up. Please note the figures obtained for Au, Ag, Cu, Co, and all
of the M-state elements. The only way to determine if they are present
at this point in times seems to be to reduce them to metal and attempt
The major purpose in all of this, for me personally was along this line
The Essene said that the black sand that he was providing was not going
to be available forever...There is a need to find a replacement or
probably something better :) I first began all of this Work with the
mind set that if I find a source material which is most abundant in its
ORME content then we would have the best medicine. Well, so far it
hasn't worked that way but that was the reasoning behind it. All of
this Work has definitely improved my processes and the potency and
purity of my Manna so there has been significant benefit.
Much more research needs to be done.
1) Assay the starting material.
2) Precipitate it and remove the precipitate slurry and assay it.
Standard Wet Method was used.
3) Dry a sample of the same slurry under UV or direct sunlight. This
should, according to Hudson and the Essene BEGIN its transformation to
a metallic ground state or platform. Assay it.
It is worth mentioning here that the Essene said that there were two
primary platforms which are gold, Au and palladium, Pd but that silver,
Ag was the very first to give up its "spin" and become more metallic.
This actually seems to agree with my later assays which will be shown
4) Mix some of the same sample with sulfur and fire it at a high
temperature. Put some away, and the rest Assay it. The reasoning
being that the sulfur steals the sodium off of the ORMEs at high heat
and they have no choice then but to begin to form metallic bonds. Well,
it may not be quite like that but I did it this way, which is very
similar to what King Solomon's process was reported to be.
5) Wait 6 months to a year and assay some of the same material from
step 4. David Hudson and the Essene both say that it takes a year
to "mature." AND sure enough, the material kept changing.
This above procedure was used to begin this Work...with both minor and
major tweaking :-)
I'll take a break now and ask Barry to also make available the Assays for
the following two samples:
RDL ................... Red Devil Lye
SMARTFG ....... Smart brand food grade muriatic acid from Lowes home
Once all of this is available, I'll continue. Please hold most
questions until you have looked at all of the Work and understand the
As previously written, the flow of the Work is:
1) Get source material and Assay.
2) Precipitate it, separate the precipitate and Assay a sample of it.
3) Dry it under UV light or direct sunlight. Take a sample and Assay it.
There is more:
4) Burn it with sulfur or torture it in some other way which should
reduce the ORMEs to metal. Assay that...setting some aside to age.
5) Let it mature for 6 months to a year and Assay it again :)
I should also note that none of these assays are from a MSDS, I paid
for these assays directly.
For most of this Work I was using Masada dead Sea bath salt, unscented.
The assay for this salt dissolved into commercial distilled water is
I took this salt and water and precipitated it with Red Devil Lye
solution (RDL mixed into distilled water at 125 grams per liter) as per
the normally accepted Wet Method.
an assay of this solution. Red Devil Lye.
I let it precipitate and settle at about pH 10.7...when you are
precipitating this material you get to a "plateau" where you are adding
RDL solution but the pH is not rising. This energetic phenomenon seems
to indicate the presence of ORMEs/M-state. Once you eventually go past
this plateau the pH begins to rise quickly or spike upwards. I stop
I let the precipitate settle overnight and carefully pour the clear top
I take just the precipitate and slowly add a 6N (about 20%) HCL
solution made from the SMARTFG (food grade muriatic acid-Smart brand)
while stirring like crazy and slowly reduce the pH of the slurry to
around 8.0 - 8.5 (it wants to creep around a bit :)
An assay of this solution is sample SMARTFG
(Smart brand food grade muriatic acid).
I let the pH adjusted slurry settle and separate it from the clear top
water and wash it one time with three times as much distilled water as
precipitate by volume.
I let it settle overnight again and separate it as the Materia.
I send a small portion of this off for Assay.
Sorry I don't have an assay of this phase available yet...My old
computer ate it when it died and I am resubmitting a sample.
Next, I take a large sample and dry it under UV light. For this Work in
particular I used a pair of 75 watt black lights under reflectors and
the Materia was placed into a white casserole dish. The color may help
to reflect some of the light rays back onto the Materia. I just let it
sit there until it is thoroughly dry...usually 7 days, depending upon
relative humidity and ambient temperature of the room, then I scrape it
out with a stainless steel putty knife and grind it all up in a marble
mortar and pestle.
I send a sample of it off for assay.
Sample DSU.VPH8 is this material.
If you compare this with the initial assay (MAS106) you may begin to
see what I have been looking at.
The Ag has gone from <0.05 ppb to 6.0 ppb
Au has gone from 0.31 ppb to 46.6 ppb.
Cu, Ni, Co everything is showing up more now.
I took some of the Dead Sea Brine, the actual whole Dead Sea water and
did all of the above to it.
The only difference was that I took the wet precipitate and continued
washing it until there was no taste of salt in the clear top water
before I dried it under the same light kit as previously mentioned for
7 days. I ground the Materia up in the mortar and sent it off for Assay.
Hummm...less Ag and more Au. than the DSU.VPH8 sample and still quite a
bit of sodium (Na). It was washed profusely compared to the DSU.VPH8
sample so something is holding the salt...I couldn't taste it at all.
Now the next phase of the Work begins to get really interesting...to me
The Essene and David Hudson had both pointed to several catalysts which
make the ORMEs fall to metal. I always use the term FALL to metal but
not to irk the chemists here ;-) because technically speaking, the
metallic form is a higher energy state. However, my body and my
consciousness tell me otherwise :)
Metal IS the fallen state/form, IMO
What they had both pointed to was:
UV or sunlight...I can tell you that if you leave this Materia in the
light for a long time, it gets more and more metallic.
The FORM does not end with my assays...nor does the change in form.
Sulfur and sulfites are another catalyst which they both pointed to for
causing metallic bonding.
I took some of the UV dried Material, weighed out 40 grams, mixed it
intimately with some garden variety sulfur, specifically Dragon brand
of powdered sulfur which I got at a Home Depot or some other like place
and mixed 40 grams of it in, the assay on the bag said 95% sulfur and
listed no metals, but I never assayed it. It costs about $4 for 4
pounds, so I am certain it is just loaded with goodies like platinum
and Iridium...NAH...just jesting :)
I placed this into a stainless steel pot, covered it with a stainless
steel lid , placed it over a 170,000 BTU propane burner and burned it
full throttle for about 1/2 an hour.
The sulfur goes up pretty quickly and so does the temperature. The
bottom and sides of the pot were cherry red. I found out in subsequent
experiments that this is not hot enough to melt Cu, Ag or Au metals.
This process using the tools I was using could not really replicate
Solomon's Work which involved the actual smelting of the metals.
So, I figured that any gold or silver which came out of the pot most
likely had to have been from M-state elements and/or mostly through
Since I had seen gold form onto a propane burner during an M-3 sodium
burn where the temperatures were not hot enough to melt gold, let alone
boil and vaporize it, (which is about the only way that I know of for
condensing gold metal from metal onto a nearby cold spot, like a
propane burner which is itself cooled by the gas which feeds the fire)
I have been aware of the possibility that these fire processes actually
vaporize some of the M-state. Then it can condense into either the
metallic form or back into the M-state, depending upon which condition
necessary for which formation is the most prevalent. Sometimes it seems
to do both.
(M-state gold vaporizes at just 425 degrees C...which is exactly why
M-state gold will not show up in a fire assay...it gets lost to the
vapor phase of the roast!)
We sent a sample of this burn off for an assay and the fire assay came
0.4 Oz./ton Ag ....that is 9600 ppb
0.04 oz/ton of Au ...this is 512 ppb
Humm! The initial assay of the source material said less than 0.05 ppb
of Ag and 0.31 ppb of Au.
The dry white powder before burning weighed 40 grams. I really don't
know what it weighed after burning because I no longer have those notes.
But, we are in the process of retrieving this assay as the copy is
still in Virginia.
Take a look at sample:
This is the very same materia...a little less than a year later.
Is Transmutation Just Accelerated Evolution ?
Is Transmutation actual manifestation by condensation?
So now we are at a point where we are intending to reduce this material
to a metallic form no matter how violent we need to get to accomplish
The Essene said that King Solomon would use the top layer of the white
precipitate powder which had been dried by the baking sun.
He would mix that with brimstone and reduce it with iron in a
reverbatory furnace, using silver as a collector of the gold and using
iron to scavenge-collect the "trash" metals.
I did a few experiments using silver shavings and once or twice a
silver coin but never got enough heat to melt these using the tools
available to me.
Smelting metals has never held much appeal to me and really good
furnaces are beyond my budget but we'll talk about that Ag coin a
little later on.
So far it seems that what the Essene and David Hudson both had to say
about these materials has validity.
Something that the Essene said a telephone conversation really confused
me. He said that these elements change from the nucleus and he even
sent a clear mental picture to me. I could *see* what he was telling me
but still did not understand what it meant.
I began investigating isotope data from the Sheffield computer in
England. At http://www.webelements.com/
if you engage the Professional Edition you will find links to the
currently accepted isotope data to the left of each individual
elements' description page.
For instance, if you click on Ag there is a link on the left hand
column, near the bottom, for isotope data.
There are links for Natural isotopes and for Radioisotopes.
The Essene and David Hudson said that when you try to force this
material to metal that there is radiation emitted.
This pointed me to the radioisotope data.
Suppose you are interested in transmuting mercury (Hg) to gold (Au).
Looking at the radioisotope data for Hg (which is atomic weight 200.59)
you find four listed, from lightest to heaviest:
The mass, half-life, mode of decay, nuclear spin and nuclear magnetic
moment data are all listed there. If you don't know what they mean you
may wish to read about them at the Webelements site.
What is worth a hard look at is the Mode of Decay information.
Understanding that this data was obtained artificially is also worth
noting. That information does not include what may be happening in
Nature but gives us an illustration, if you will, of what "may" be
happening all day, every day, in Nature.
Looking at 197Hg, it tells us that its Mode of decay is:
EC to 197Au.
So, with a change in electron configuration 197Hg becomes gold. It just
needs some excuse to change its electron configuration (EC) as it
already has the correct nucleus for gold. The data specifies that it
has a Half-life of 2.672 days.
If you were to want the chosen element to gain weight, then that is
almost always where the radiation emission occurs.
The isotope 203Hg, still mercury but is "heavy mercury" can move to
203Tl (Thallium) with a Beta radiation emission.
Looking at other elements...listing up /down in weight:
Gold moves down to platinum with EC.
Gold moves up to mercury with beta emission.
Silver moves up to cadmium with beta emission.
Silver moves down to palladium with EC
Palladium moves up to silver with beta emission.
Palladium moves down to rhodium with EC.
What the Essene and David Hudson were both saying is that this type of
thing is occurring constantly in nature.
The Works published by C. Louis Kervran in France prove Biological
Transmutations back in the 1940's but his numbers were so small,
literally reporting in milligrams, that his information has largely
been ignored by Western man. It would appear that Americans like
"sensational" numbers or they will just ignore some of the most
important Work ever performed.
Lately, medical science has rediscovered his Work and rightly so, as it
shows us how living things change one element into another element
Getting back to the Work at hand...
When I mixed the white powder with sulfur and fired it at high heat it
produced a little bit of Au and little bit of Ag. It also produced some
form of radiation. After doing this a few times, along with being
exposed to noxious sulfur fumes and probably a host of monoxide gasses,
I became deathly ill.
So I don't do that anymore :-)
I immediately sent a sample off for fire assay...the results came back
0.4 oz./ton of Ag.
0.04 oz./ton of Au.
As previously mentioned I am attempting to get a copy of that assay.
(Chris Cristopherson performed it.)
The assays for MULTIBURN are assays of the Masada Dead Sea precipitate
burned as said above. After more than a dozen different burns, where I
would look at the material each time to see if anything different
occurred, I would just dump the sulfide mat into a plastic HDPE bucket
and cover it with its lid. It was all the same Materia pretty much
treated the same way. No metals were added at any time. The variations
were the amount of white powder in relation to the amount of sulfur
When I sent the sample out for assay I stirred the entire mess up and
took a portion from the bottom, some from the middle and some from the
top. The material had been sitting for months in the dark, with its lid
If you look at the results, one thing is quite obvious, the amount of
silver greatly increased. So did the Au. Also, platinum and palladium
suddenly "show up!"
Something else to notice is that boron really grew! Boron isn't
normally considered an ORMUS element. Yet many of these other elements
Things that make you say "Huh?"
I could tell you that I think that during the burns, since there is a
tight lid on the crucible that the ORMEs are largely vaporizing and
recondensing again as the burn cools.
Those burns did not get hot enough to vaporize m-rhodium, m-iridium,
and several other M-elements which I am certain are actually still
there in the mix. But since they are invisible to assay I'll not be
able to prove or disprove this possibility until I can get some better
So the Work need to go onward.
The door has been opened and progress has been made. It took four years
to get this far. Yet the evidence is irrefutable.
When you look at a burned sulfide mat it is an ugly, black, stinking
mess. If you are expecting to see bright, shine gold and silver you
would be very disappointed. What you will see are mostly oxides of the
elements and the only way to what you may have is to assay it.
Fire assays don't lie. They will show you the gold and the silver
(metal) that other scans will miss. However, they will NEVER show gold
and silver that is not there.
I have taken Silver from Masada Dead Sea salt solution which assayed to
contain < 0.05 ppb (parts per billion) of silver (Ag) and have
gotten 279.408 oz./ton from it.
I have taken gold from Masada Dead Sea salt solution which assayed to
contain 0.31 ppb (parts per billion) of gold (Au) and have gotten 1.4
oz./ton from it.
Yes. There are ORMEs in sea salt.
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