mono atomics

8/12/2019 Mono Atomics

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The Grail Vine is a newsletter which passes on materials to the Grail Ring. GrailZine is the electronic magazine of the Grail Ring. Grail News Now or GNN is itsnews service. Most Grail Vines and Zines are available when one has done theDI M!ND "!D# Training with nanda$%mman&el' which entitles one to a&tomatics&bscription to these p&blications.

(ome of the material within these p&blications come onto the web site' and &s&all)* months to a )ear later. +ere is one Grail Vine. s the earl) Zines and Vinespoint o&t' Tr&th Is ,l&ral' let )o&r own &ni-&e tr&th g&ide )o& b)...

ll of the Grail Ring do not &se these elements witho&t Internal lchem) b) wholebod) ,hase /on0&gation' or Diamond "od) Vorte1i0ah b) compassionate ecstasis. swith the (omegenics with which the Gold is added Dail) practice comes first'there is no short c&t in alchem). "e a /oherent 2ni ,+Ier of 3Ma4ing the Innerli4e the o&ter' and the o&ter li4e the inner.3

GR I5 VIN% 66

(2,%R/!ND2/TING G!5D 7R!M (% 8 T%R

T+% 5/+%MI/ 5 (T!N% 7R!M (% ( 5T

Dear %nGrailed brothers and sisters. fter hearing that some brothers and sistershave still been &sing the %theri&m and Isis 8hite Gold so&rces' which we have beenrepeatedl) rela)ing' for at least one )ear' contain radioactive ingredients' wesend this posting' which tells one +!8 T! %9TR /T T+% M!N! T!MI/ (2,%R/!ND2/TING

5/+%MI/ 5 %5%M%NT( 7R!M (% 8 T%R. #es' 0&st as the n&na4i master lchemist%n4i$,tah' according to the most ancient (&merian :ings lists' e1tracted gold fromsea water.

,lease investigate an) so&rce of monatomic elements' and consider that 6 )ear ofradioactive elements and heav) metals will not brea4down' and ma) reach adangero&s level after one )ear s&plementation. Treat this s&b0ect with wisdom'this is not 0&st a vitamine.

The reason one ma) feel high with radioactives is that the life force is beingreleased from the cells' the same mista4e made b) the Taoist alchemists accordingto their archaic literat&re. In other words' the) are slowl) d)ing' li4echemotherap). The best wo&ld be to 1tract the stone )o&rself with /onscio&s Intent

of the ;&ant&m observer in the heating process' so&nd' and heart coherence.

#o& ma) want to &se the dead sea salts' or lpine mo&ntain waters' or othervolcanic la4es' (alt 5a4e /it) salts can also be &sed. http


2/36

Instead of ?@&st sa) No'3 3@&st (a) :now.3

!ne lchemist colleag&e in Denmar4 has s&ccessf&ll) isolated the white powder goldfrom Dead (ea (alt' it tastes li4e (weet (perm' 0&st li4e the Green Valle) Tr&stManna. fter A months it tastes li4e washing powder' 0&st li4e Green Valle) Tr&stManna' and other lchemists e1tractions available non commerciall) b) membership.+e said it was ver) simple indeed.

ll Is God lchem) "e #o&' )e Merlin?s' and #e #eshe?s' /ompassionatel)...

5ight' 5ove' 5ife'

nanda' 7ebr&ar) 6Bth' C

!RM2( = 5> /+%M =Meia>

,R!D2/TI!N T%/+NI;2%(

This doc&ment ma) not be reprod&ced e1cept in its entiret)' and witho&t

changes. "efore tr)ing an) of the proced&res described in this doc&ment' we

advise )o& to thoro&ghl) read this doc&ment several times.

This doc&ment was created b) a gro&p of people who believe that this

information is of inestimable val&e to h&manit) and sho&ld be made widel)

available as soon as possible. The information here is declared to be in the

p&blic domain and we wish that it not become the sole propert) of an)

individ&al or gro&p.

+ere we describe some simple wa)s of ma4ing !RM2( so that readers can

begin tr&e scientific and int&itive e1periments with these materials.

ll of these methods are e1perimental. The following information is presented

to promote scientific research into the nat&re of these materials. ltho&gh these

methods are based on o&r best 4nowledge at this time' f&rther scientific research


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ma) prove some of these processes or theories to be inacc&rate.

DI(/5 IM%R

The processes described here have not all been tested e1tensivel). 8e do not

g&arantee the proced&res in this doc&ment' nor the res&lts obtained b) &sing

them. To the e1tent that )o& &se or implement these proced&res or the prod&cts

thereof' )o& do so at )o&r own ris4. In no event will the a&thors of this

doc&ment be liable to )o&' an)one else' or an) organization or government' for

an) damages arising from )o&r &se' or )o&r inabilit) to &se these proced&res or

the prod&ct thereof. ppl) these proced&res at )o&r own ris4.

V%RI7I/ TI!N

The material made b) some of these methods has been tested b) an independent

lab &sing 9 ra) fl&orescence and photo spectrometr) to identif) the emission

spectra of m state materials. =The lab prefers to remain anon)mo&s>. The

m state spectral emissions signat&re was a broad' flat band rather than discrete

lines. The test also showed a significant amo&nt of calci&m and magnesi&m' b&t

no to1ins were evident in well washed material made from &npoll&ted ocean

water.

To f&rther prove that these materials are a different state of the precio&s

elements mentioned above' it is possible to electroplate these elements o&t as

precio&s metals.

,eople familiar with +&dson?s process claim that the materials prod&ced &sing

these methods are similar to +&dson?s !RM% materials.


4/36

ING%(TI!N

8e do not recommend the ingestion of these materials since so little is 4nown

abo&t them. This information is being provided so that scientific in-&ir) can

commence into the nat&re of these materials. 8e realize that' despite

recommendations to the contrar)' some people will ingest these materials. 8ith

this in mind we offer the following information to minimize an) possible

adverse effects from ingesting these materials. ,lease read the 8 RNING and

/ 2TI!N sections.

(ome people have ingested the m state materials made b) these methods. The)

s&ggest that benefits are most li4el) when dosage is 4ept small.

Three methods of ma4ing !RM2( are described in this doc&ment< the 8%T

method' the DR# method' and the "!I5ING G!5D method. 7or the materials

e1tracted b) the wet and dr) proced&res' one teaspoon of material' morning and

evening' has been fo&nd b) them to be not harmf&l over several wee4s? time.

m&ch smaller dose' on the order of a few drops a da)' wo&ld be more

appropriate for the material prod&ced b) the boiling gold method. 8e believe

that the m state ma) be homeopathic' so a m&ch smaller dose ma) be the safest

s&ch as 6$*E teaspoon dil&ted in one -&art of p&re water' ta4en two or three

o&nces once or twice a da).

David +&dson gave some information on dosage in his Dallas speech atC m&st be present in the starting material.

=(ince the "oiling Gold method is effective witho&t an) magnesi&m' this claim

will need to be tested.> (ea water alread) has Mg=!+>C' so )o& don?t need to

add it to sea water. Tr) )o&r water first. If )o& don?t get an) precipitate' )o&

might add a teaspoon per gallon of %psom salts to the starting material for its

magnesi&m. If )o& do add %psom salts' the magnesi&m from them will be a

large portion of the precipitate.

8 RNINGKK

,R!"5%M( %N/!2NT%R%D

The following problems have been enco&ntered b) some fol4s who have made

m state for cons&mption.

"oiling in l)e water 4ills bacteria b&t it does not destro) to1ic metals or


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chemicals in )o&r so&rce water.

7ollow these instr&ctions and slowl) change the p+ of )o&r sol&tion.

void water with s&lf&r or s&lfates in it beca&se s&ch water prod&ces

little or no m state precipitate.

Never &se al&min&m containers or &tensils beca&se al&min&m will react

with acids li4e +/l and al4alis li4e l)e' and co&ld poison )o&.

!RM2( /+%MI/ 5 ,R!D2/TI!N T%/+NI;2%(

/!NTIN2%D...

L"ac4 to first page L"ac4 to previo&s page

8et Method ,roced&re

+ow to ,&rif) #o&r ,recipitate Removing Mg=!+>C

6. Method 6

C. Method C

A. Method A

E. Method E

Dr) Method

6. %1tra (&pplies

C. +older 7or 7ilters

A. (tarting Materials

E. ,roced&re

"oiling Gold Method

6. %1tra (&pplies

C. ,roced&re

ppendi1

6. M state (torage

C. /hemical (&ppliers


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A. 5ab (&pplies

E. (tarting Material (o&rces

8%T M%T+!D ,R!/%D2R%

,lease read / 2TI!NKK and 8 RNINGKK before proceeding.

7irst )o& need to prepare a dil&te l)e sol&tion. 5abel an e)edropper bottle or

s-&irt bottle 35)e poison3 so the bottle will not conf&sed with something else.

8or4 in a sin4 so that an) spills will be contained. 5)e gives off e)e stinging

f&mes when mi1ed with water. To avoid inhaling f&mes' hold )o&r breath and

wear goggles while doing the following proced&re.

8or4ing over a sin4' p&t H teaspoons of distilled water in a st&rd) glass then

stir in 6 teaspoon of l)e. (tir &ntil the l)e is dissolved. +eat will be generated

as the l)e dissolves and the glass ma) get fairl) hot. #o& ma) want to close

)o&r e)es to avoid e)e stinging f&mes' ta4ing a pee4 periodicall).

,o&r the l)e sol&tion into a labeled e)edropper bottle or s-&irt bottle.

If )o& are &sing p+ paper' tear off several 6$E3 pieces and p&t them on a piece

of white paper on a plate.

7or the best acc&rac)' recalibrate the p+ paper thro&gho&t the da) with changes

in temperat&re and h&midit)' as well as da) to da). "&ffer sol&tions of p+ E'

and 6 will help with this. (o&rces of p+ b&ffer sol&tions are listed near the

end of this doc&ment &nder 5 " (2,,5I%(.


16/36

If )o& are &sing dried sea minerals' mi1 6$C c&p of dr) material with C c&ps of

distilled water. This ma4es sea water. Now proceed as described below before boiling.

!nce the precipitate and water have been sterilized' the ne1t step is

re-&ired to concentrate the m state.

+!8 T! ,2RI7# #!2R ,R%/I,IT T%

The precipitate made from sea water contains mil4 of magnesia

=Mg=!+>C>' which precipitates appro1imatel) aro&nd the same p+

range that m state does.

+ere are fo&r methods to separate Mg=!+>C from m stateC.

C. 2se a s)ringe to remove the li-&id over the precipitate' and

discard the li-&id. This leaves onl) the m state$Mg=!+>C

precipitate.

A. To the wet precipitate' add h)drochloric acid =+/l> &ntil )o&

red&ce the p+ to 6. A.F. #o& can &se m&riatic acid =A6

+/l> from a hardware store' b&t lab grade +/l is less li4el) to

be contaminated. safe alternative to +/l is distilled white

vinegar.

E. The white colloidal precipitate sho&ld dissolve' leaving a

clear sol&tion.

F. dd l)e sol&tion V%R# (5!85# drop b) drop to bring

the p+ bac4 &p to H.F H. . The precipitate that forms sho&ld

be m state mostl) free of Mg=!+>C =beca&se m state

precipitates in this p+ range' and Mg=!+>C does not

precipitate &ntil p+ B.>

Note that )o&r total )ield ma) be diminished beca&se )o& are

not going past p+ H. .

*. Remove the li-&id above the precipitate' and wash the

precipitate. It sho&ld be mostl) m state.


21/36

M%T+!D C

This proced&re removes the Mg=!+>C b) dissolving it below

p+ B. 7irst get some +/l =or m&riatic acid> and coffee filters.

safer alternative to +/l is distilled white vinegar.

6. Dr) the precipitate in a dar4 oven at abo&t C F degrees 7 for

one or two ho&rs. This forms a dr) powder.

C. Ta4e the dr) powder and p&lverize o&t an) cl&mps.

A. In a glass container' cover the powder with some distilled

water. 7or e1ample' one liter of water for one c&p of powder.

E. dd +/l or distilled white vinegar drop b) drop to bring

the p+ to F or *.

F. (ha4e the bottle and let it sit overnight. The dried m state

sho&ld not dissolve at that p+' b&t the Mg=!+>C sho&ld

dissolve.

*. The ne1t da)' after all the Mg=!+>C has dissolved' po&r

ever)thing into filter paper.

. 8ash the powder collected in the filter paper several times

with distilled water to remove an) resid&al traces of +/l or

vinegar.

H. The washed powder ma) be oven dried again at abo&t C F


22/36

degrees 7' and )o& sho&ld have m state powder free of

Mg=!+>C.

M%T+!D A

6. Dr) the original precipitate at abo&t C degrees 7.

C. Mi1 the res&lting powder with distilled white vinegar or

A +/l. %ver)thing which does not dissolve in m state. This

will be -&ite a small amo&nt if )o& start with sea water. =If )o&

mi1 p&re +/l with distilled water' remember< DD /ID T!

8 T%R' N%V%R DD 8 T%R T! /ID>.

A. Meas&re the amo&nt of +/l$m state sol&tion =or

vinegar$m state sol&tion>.

E. dd distilled water to the +/l$m state sol&tion. dd an

amo&nt of water that is at least ten times the amo&nt of

+/l$m state sol&tion. =#o& ma) s&bstit&te distilled white

vinegar for +/l>.

F. 7ilter the sol&tion thro&gh F la)ers of coffee filters.

*. 8ash the powder at least three times in a large amo&nt of

distilled water.

M%T+!D E

6. (tarting with clean wet precipitate' add l)e to bring the p+


23/36

&p to 6C. The m state precipitate will dissolve' b&t magnesi&m

h)dro1ide and the Gilcrest precipitate will not.

C. 7ilter o&t the precipitate.

A. To the remaining li-&id containing onl) m state' add +/l or

distilled white vinegar drop b) drop &ntil the p+ reaches H.F.

E. dd l)e sol&tion drop b) drop to bring the p+ bac4 &p to

6 . H. The res&lting precipitate sho&ld be onl) m state.

F. 8ash the precipitate as described earlier.

*. To be safe' chec4 the p+ of the precipitate sl&rr). It sho&ld

be B or less before ingesting.

DR# M%T+!D

,lease read / 2TI!NKK and 8 RNINGKK before proceeding.

This method ta4es longer than the 8%T method. In some cases' it

involves boiling l)e for several ho&rs' which ma) spra) some ca&stic

sol&tion aro&nd )o&r wor4 area. ,lease wear neoprene gloves' a ,V/

lab apron' and e)e goggles when )o& &se this method. (o&rces for this

safet) clothing are listed near the end of this doc&ment &nder 5 "

(2,,5I%(.

(ome people have reported adverse reactions to the 8%T method


24/36

precipitate or powder. This ma) be d&e to the Gilcrest precipitates

which occ&r above p+ 66.F. The DR# method removes the dangero&s

Gilcrest precipitates' so it res&lts in safer material.

%9TR (2,,5I%( N%%D%D 7!R T+% DR# M%T+!D

6C c&p coffee filters from a grocer) store.

+)drochloric acid. #o& can &se m&riatic acid =A6 +/l> from a

hardware store' b&t lab grade +/l is less li4el) to be contaminated.

!ther acids can be &sed' b&t +/l will not harm the bod) if accidentall)

ingested in wea4 sol&tions and in small amo&nts. #o& might prefer to

&se distilled white vinegar instead of +/l. ltho&gh distilled white

vinegar =acetic acid> is wea4er than +/l' is it safer to wor4 with.

+eav) plastic +D,% cottage cheese containers' 6 pint and 6 -&art' to

hold the coffee filters.

M :ING +!5D%R 7!R T+% /!77%% 7I5T%R(

6. (tart with a pint and a -&art container for cottage cheese.

Ma4e s&re the pint container will fit into the -&art container.

The pint container sho&ld hang inside the lip of the -&art

container.

C. cross the bottom of the pint container' p&nch or drill

several holes' 6$H3 to 6$E3 diameter' abo&t 6$E3 apart.

A. If the small container fits too tightl) into the larger container'


25/36

)o& ma) need to drill some air press&re e-&alization holes

aro&nd the o&tside of the large container near the level of the

bottom of the small container. !therwise the air press&re

between the two containers will 4eep li-&id from draining from

the coffee filters. 8hen )o& &se this filter' place the cottage

cheese containers in a stainless steel or glass container to catch

an) overflow. The l)e water that )o& will be filtering ma)

damage co&nter tops or cabinets if it contacts them.

E. The coffee filters sho&ld fit nicel) into the smaller top

cottage cheese container.

DR# M%T+!D (T RTING M T%RI 5(

Generall) start with dr) material s&ch as sweepings from salt and al4ali

flats' roc4 powders' limestone' mineral salts' Isis or %theri&m white gold

powder' volcanic ash' plant cinders' etc.

These are some materials that prod&ce a lot of precipitate from the DR#

method

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