RE: CSCC CS for swimming pools

2002-05-22 Thread I Anderson
Hi Marshall,

I think you are forgetting about the solubility of silver chloride.
At 1 ppm Cl about 0.7 ppm of the silver will remain dissolved,
halve the amount of chlorine and double the amount of silver will
remain dissolved.

Ivan


 -Original Message-
 From: Marshall Dudley [mailto:mdud...@execonn.com]
 Sent: Tuesday, 21 May 2002 4:07 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CSCC  CS for swimming pools


 Normally the amount of chlorine is on the order of 1 ppm.
 One ppm of chlorine
 will react with about 3 ppm of silver (by weight).  A pool
 containing 20,000
 gallons of water with 1 ppm of chlorine would have sufficient
 chlorine to react
 with half a pound of silver making about 2/3 pound of silver
 chloride.  I would
 hardly call that insignificant.

 Marshall

 MARIANO DELISE wrote:

  It needs a very SMALL amount of chlorine to burn off all
 the dead critters
  killed by the silver.  Not enough to make much silver chloride
  - Original Message -
  From: natural_essenti...@juno.com
  To: silver-list@eskimo.com
  Sent: Sunday, May 19, 2002 8:18 AM
  Subject: CSCC  CS for swimming pools
 
   Hi all,
  
   I've been looking at some ionizers for swimming pools.
 The majority of
   sites say that some chlorine is still needed weekly.  It
 would seem to me
   that the chlorine and silver would make some silver
 chloride.  Please
   correct me if I'm wrong, but I thought that silver chloide was
   poisonous/toxic?
  
   Does anyone currently use an ionizer in your pool/spa,
 and how satisfied
   with it are you?  I seem to recall the original thread
 was posed by
   Marshall.
  
   Leacy
   Life is Good!
  
  
   
   GET INTERNET ACCESS FROM JUNO!
   Juno offers FREE or PREMIUM Internet access for less!
   Join Juno today!  For your FREE software, visit:
   http://dl.www.juno.com/get/web/.
  
  
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CSSTD's was CSzapper

2002-05-22 Thread I Anderson


 -Original Message-
 From: Joyce Inouye [mailto:jinou...@ccsf.cc.ca.us]
 Sent: Monday, 20 May 2002 4:04 p.m.
 To: John Reeder
 Cc: silver-list@eskimo.com
 Subject: RE: CSzapper


...
 Sex is an easy way to get cancer germs and parasites into your
 body.  About ten (10) HIV viruses can fit the diameter of the
 average hole in a condom.  Those who teach kids to use condoms
 are indirectly spreading deadly germs such as HIV and
 cancer-causing germs among the young people.  Teaching kids to
 have sex with condoms increases venereal diseases among them, and
 venereal diseases are linked to cancer.

What sort of logic is that.

Those kids who use condoms are preventing a great percentage of the
sexually transmitted diseases that would otherwise be spread if they
didn't wear them! This actually decreases the incidence of venereal
diseases among them.

Ivan.


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RE: CSPhototherapy Light Wand Assembly Instructions

2002-05-13 Thread I Anderson
The LED modules you guys are looking at are not really intense enough
for low level light therapy (LLLT)

The Jameco part has a maximum intensity of 12,000 mcd

The BGgmicro parts have a maximum intensity 7,700 mcd

Whereas the Digikey part (67-1589-ND) has a max intensity of 48,000
mcd and is much more likely to produce results.

I have single red LEDs that produce 6,000 mcd.

Search for LLLT (many hits for laser, but the coherency of the light
is lost as it enters the tissue and LEDs do just as well). Also try
LED phototherapy.

This is a well researched and serious treatment modality. Visible red
light (660nm) penetrates the tissue 25 - 50mm and interacts with the
mitochondria directly, causing an increase in cellular energy
production, and increased rates of DNA and RNA transcription, (i.e.
increased healing) among other things. Near infrared (700 - 800nm)
interacts with the cellular membranes, causes the production of
singlet oxygen radicals (at levels high enough to oxidise pathogens
but not high enough to cause cellular damage) and increases the
potential difference across the membrane allowing for optimum entry of
nutrients and expulsion of waste.

Apart from Brook's highly innovative and important use of this simple
technology, red light can be used to halt bruising (use instead of
ice) limit or halt inflammation, lessen pain, and speed healing of
sprains, contusions, ulcers and so on.

My units are in constant use by the family and friends, and now my
daughters school is wishing for a unit (which I will donate) ever
since I brought a portable one to the sick bay for my daughter to use,
a boy had dropped a chair on her toe. Within minutes of use (the
school reports) the pain and swelling had gone, the shoe was on and
she was outside with her team having netball practice.

One would do well to build a LED phototherapy unit.

Ivan




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CSWater Diffusion

2002-05-11 Thread I Anderson
I have been studying the diffusion of water into the body and cells,
mindful of the comments of Dr Batmanghelidj (Your Bodies Many Cries
For Water) which in essence says  that, as water is accepted into the
body via the cells one molecule at a time, there is no point in
drinking structured water or any other 'special water' (at least not
for the water content) because these structures are broken up and any
mineral or other content stripped from them before the water is
absorbed.

I have a couple of highly technical papers that describe the structure
of a fairly recently discovered class of cellular pores called
Aquapores (funnily enough), which do indeed restrict the entry of
water to single file.

However I did come across this site which explains the implications of
this discovery in an amusing and non-technical manner.

Enjoy! http://student.biology.arizona.edu/honors98/group6/

Ivan.


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RE: CShype or not...

2002-05-06 Thread I Anderson




 -Original Message-
 From: Rich Adams [mailto:r...@kc.rr.com]

 More hype?
 http://www.purestcolloids.com/ionic.htm

Yes.

1. I know of no research that compares the effectiveness of silver
chloride vs true silver colloids. Silver chloride is known to be
mildly anti-bacterial in vitro, silver ions are a far more
anti-bacterial than true silver colloids in vitro.

2. A high percentage of ingested silver ions are absorbed into the
blood stream, whether as silver chloride or some amino acid chelate.
This is shown to be true by an investigation into a largely ionic CS
written by Roger Altman (ex list member), and ironically, a copy can
be found on the silver-colloids web site.

3. All so called colloidal silver, other than Mesosilver true colloid,
the silver proteins and other silver complexes, have a high ionic
content. Most of the testimonials regarding the effectiveness of CS
refers to the high ionic variety, even those that could be found on
sites selling mesosilver.

4. The fact that a child can do it makes this valuable supplement
available to all, and not just those with a deep wallet.

My opinion only,
Ivan.




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RE: CSCA on eyelid

2002-05-05 Thread I Anderson
Might I suggest the use of beta glucan mixed with aloe vera for
application to the eyelid. Many studies on this substance, but still
widely unknown. Proven anti-cancer properties (one detailing resolving
melanoma by direct injection into mass), best immune stimulator
available.
Beta glucan (mixed with d. water) can be used in the eye also.

Will aid healing even if other remedies are used.

Ivan.

 -Original Message-
 From: d.linen [mailto:li...@flash.net]
 Sent: Sunday, 5 May 2002 9:08 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CSCA on eyelid


 Which eyelid? Mine is on my lower eyelid right now. I've been using
 Cansema, a black salve. You can put it up to 1/4 inch from
 the eye. BUT
 you can use the liquid Cansema on the eyelid and around the
 eye with no
 problem because it's not caustic like the salve is. I had a
 huge cancer
 that was about the size of a credit card under my left eye
 and now it's
 about 75 percent improved over a year ago. I just can't quite get
the
 salve that close to my eye or it would be healed by now.

 I take the Cansema capsules too.

 Connie wrote:
 
  From a friend
 
  ...The doctor decided one of the lumps on my eyelid is
  cancer   :-(
 
  I was told a Dermotologist would do the eye,,,then the
  Opthalmologist said I needed a Plastic Surgeon,,, and the
  Plastic surgeon thinks they and the Opthalmologist have
  to work together for different things!
 
  Any suggestions for a friend? Would Black salve be OK that close
to
  the eye?
  She is a believer in CS, but not sure if she has any trust in
other
  alternative treatments.
  Connie


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RE: CSCA on eyelid

2002-05-05 Thread I Anderson
Oops!
find beta glucan here:
http://www.chisolmbio.com/

Ivan

 -Original Message-
 From: I Anderson [mailto:i...@win.co.nz]
 Sent: Sunday, 5 May 2002 10:35 p.m.
 To: silver-list@eskimo.com
 Subject: RE: CSCA on eyelid


 Might I suggest the use of beta glucan mixed with aloe vera for
 application to the eyelid. Many studies on this substance, but still
 widely unknown. Proven anti-cancer properties (one detailing
resolving
 melanoma by direct injection into mass), best immune stimulator
 available.
 Beta glucan (mixed with d. water) can be used in the eye also.

 Will aid healing even if other remedies are used.

 Ivan.

  -Original Message-
  From: d.linen [mailto:li...@flash.net]
  Sent: Sunday, 5 May 2002 9:08 p.m.
  To: silver-list@eskimo.com
  Subject: Re: CSCA on eyelid
 
 
  Which eyelid? Mine is on my lower eyelid right now. I've been
using
  Cansema, a black salve. You can put it up to 1/4 inch from
  the eye. BUT
  you can use the liquid Cansema on the eyelid and around the
  eye with no
  problem because it's not caustic like the salve is. I had a
  huge cancer
  that was about the size of a credit card under my left eye
  and now it's
  about 75 percent improved over a year ago. I just can't quite get
 the
  salve that close to my eye or it would be healed by now.
 
  I take the Cansema capsules too.
 
  Connie wrote:
  
   From a friend
  
   ...The doctor decided one of the lumps on my eyelid is
   cancer   :-(
  
   I was told a Dermotologist would do the eye,,,then the
   Opthalmologist said I needed a Plastic Surgeon,,, and the
   Plastic surgeon thinks they and the Opthalmologist have
   to work together for different things!
  
   Any suggestions for a friend? Would Black salve be OK that close
 to
   the eye?
   She is a believer in CS, but not sure if she has any trust in
 other
   alternative treatments.
   Connie
 
 
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  colloidal silver.
 
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  message to:
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RE: CSPrill Thin Water

2002-05-03 Thread I Anderson
From the twilight zone
http://www.thetwilightnetwork.com


 Bath Crystals, Dollop of Love, DOL, Golden Seal Drops, Magic Oil,
Magic Water, Sea Snow, Snow Crystals, St. John's Wort Drops, Precious
Prill Beads, Laundry Bag, produced in The Star Chamber and now
available to bring The Star Chamber experience to you at home!
Can I get too much Magnesium Chloride from the products?
Prill Water - Magic Water - Magic Oil - Dollop of Love - DOL - Golden
Seal Drops - St. John's Wort Drops all have Magnesium Chloride in them
to remedy your Magnesium Deficiency for over all health and to let
your body NATURALLY raise to your normal levels.

Maybe you could add 125mg of magnesium chloride to a litre of water
for the same effect (you might need to add a little pure love energy
as well).

Ivan.

-Original Message-
From: Ian Roe [mailto:ian_onta...@hotmail.com]
Sent: Friday, 3 May 2002 12:29 p.m.
To: silver-list@eskimo.com
Subject: Re: CSPrill Thin Water


I know they say that the prills add nothing to the water but that is
not true.  I started with R.O. water at 6 ppm TDS and wound up with
water at 83ppm TDS or about 1/2 the TDS of our municipal water which
is at 170 to 190 ppm.  The nice thing was that the pH had been about
7.1 and after prilling, is at least 8 or higher (wouldn't test higher
than 8)  But it sure is cheap alkaline water. I was about to spend
$1000 or more on one of those Japanese micro machines and now I don't
have to.  The prills work great.


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CSRe: Alternative treatment - LED construction

2002-05-02 Thread I Anderson
The following is a series of messages generously sent to the list by
Brooks Bradley.
I retrieved them from my hard drive as I know how hard it is to search
the archive.

Ivan



 To all interested list members:
Recently, a rather serendipitous occurence
revealed
a possible synergistic effect through the combination of CS and LED
protocols.utilized simultaneously.
During a recent evaluation of protocols directed
toward alleviating the problems of long-term, persistent, sinus/upper
throat insults, one of our researchers experienced some unexpected
successfrom combining CS mist inhalation and LED exposure.  The
most
interesting factor being the nature of the LED array application.
During earlier experiments, it had been determined that LED exposure
(especially in the 660 to 680 nm range) resulted in very pronounced
control of upper throat pathogens.  Exposure times as short as 5
minutes, directed through the open mouth (using 5 element, 3500 mcd
Leds), achived immediate and marked relief---in an impressive number
(75%) of cases..across the entire age spectrum from 25 to 83 years
of age.  However, the success rate/degree was much less (25%)
involving
cases of deep-seated sinus insults from pathogenic/allergenic
complications.  Principally, because of the difficulty experienced in
directly illuminating the insulted tissue.
The protocol adjustment resulting in a most pronounced
improvement in frontal sinus infections/complications, sprang from the
simple application of a 15 element LED array (1.5 X 3 in area) being
held against the skin surface---first on one side directly adjacent to
the nose for 5 to 10 minutes;  followed immediately by a repetition on
the other side of the nose.  The geometry is somewhat difficult to
explain without a drawing, but imagine placing the array in such a
manner to rest one corner on the middle of the bridge of the nose
(addressed from the side) then repeating for the other side.  The
array
should placed with the long side in the horizontal  (3.5 X 1.5 )
extending away from the nosekeeping the array below the eye.  The
soft-tissue is penetrated quite well and we believe the bony
structures
may be providing some unanticipated diffusion benefits.
The throat area was treated in two ways:  First, after
a
thorough misting, with the mouth fully open, a 5 element (circular)
LED
array was used to directly expose the back of the mouth/tonsil
area.for 5 minutes.  The front edge of the array was allowed to
rest
on top of the lower front feeth. As the subject experienced saliva
generation they were instructed to  swallow---without closing their
mouth.  This had the added advantage of , momentarily, changing the
geometry of the tonsile area to give an increased exposure.
The most dramatic results accrued from the application
of the 15 element LED array on the outside of the throat area ( from
just below the jaw bone, downward).  Prior to using this modification,
we had only conjectured as to a possible benefit from such an
arrangement.  Afterward, we conducted some soft-tissue penetration
tests
using 3500 to 6000 mcd LEDs.  Even the 3500 mcd bulbs yielded .5
penetration.
   We are, at present, conducting tests to determine
the
minimum power LED that will yield positive results under similar
conditions.
A single Laser Pointer unit was tested with some,
but much reduced effectiveness .
This, combined protocol, yielded positive control
over some very pernicious---long-standing---frontal sinus insults.
Some of you may care to conduct your own
experiments
along these lines.Sincerely,
Brooks Bradley.
 p.s.  I have not forgotten my promise to post the assembly
instructions
for the 5 element LED array, contained in the pvc tubing.  I WILL try
to
get it done sometime before the week is out.



CSOT:  POSSIBLE USEFUL ADJUNCTIVE PROTOCOL

To all interested llist members.
Recently, we completed a series of evaluations
which
yielded VERY substantial results.  These evaluations were a
continuation
of earlier protocols employing LED units in experimenting for
effective
protocols.  One protocol, IN PARTICULAR.gave particularly
efficacious results.  This, experimental protocol, involved the
application of 660 nm red-spectrum light, (via both 5 bulb portable
and
larger, more powerful non-portable units).  The weakest bulbs to yield
high-quality results were on the order of 3500 mcd ( 5 bulbs arranged
in
a compact, circular assembly).  The most rapid results were achieved
with a much higher -powered (non-portable) unit of our own design and
construction.  This latter unit possesses a tissue-penetration
capability of greater than 8  -for lean-muscle tissue.  However,
VERY ACCEPTABLE results were gained from the 

RE: CSAltman article

2002-04-25 Thread I Anderson
Terry and Duncan,
Some links to info about silver selenite.



http://wlapwww.gov.bc.ca/wat/wq/BCguidelines/silver/bcsilver-14.htm#P6
23_48187
Experiments with radiosilver indicate that it is mainly associated
with the reticulo-endothelial system. The silver is concentrated in
the basement membrane of the skin, in the elastic fibres around sweat
glands and the eyes; generally in areas of the skin exposed to the
sun. The discoloured skin in argyric patients exposed to ultraviolet
radiation is likely caused by photoreduction of silver chloride to
metallic silver, which is then oxidized to black silver sulphide and
bound by tissues. If the diet is high in selenium, the silver sulphide
is converted to silver selenide which may result in higher silver
deposition rates than with silver sulphide (Danscher 1981, Berry and
Galle 1982, Buckley et al. 1965).



http://www.synthon.co.za/silver.html
a list of silver chemicals for sale, including silver selenite and
selenide.


http://www.onecachet.com/cfilmsz.htm
I. Selenium Toner

1. MACO LP Selenia is a modern selenium toner used in processing black
and white prints to improve archivality by turning the silver into
silver selenite, a compound that is more impervious to environmental
pollutants.

Selenium toning, done according to the instructions, also increases
maximum density and cleans up the whites. The chart below shows the
time/toning results ratio.

Ivan





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RE: CSa newbie here

2002-04-19 Thread I Anderson
Nice to meet you Tys, welcome!

Ivan.

 -Original Message-
 From: Tyson Brennan [mailto:tysbr...@yahoo.com]
 Sent: Friday, 19 April 2002 11:30 p.m.
 To: silver-list@eskimo.com
 Subject: CSa newbie here
 
 
 Hello everybody,
 
  I have just joined the list and I am obviously
 interested in getting a real time perspective on
 colloidal silver. I have been interested in
 alternative medicine for several years now and
 consider the prospect of becoming more knowledgable
 about as many areas as possible, well, a hobby.  I am
 most curious about validating my opinions on the
 benefits of CS which I will pretty much get from
 simply recieving posts.  Glad to be here!
 
 Tys  


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CSMSP IV HIV

2002-04-18 Thread I Anderson


Reduction of Viral Load in AIDS Patients With Intravenous Mild Silver
Protein: 3 Case Reports
Ward Dean, MD, Mark Mitchell, MD, Victor Whizar Lugo, MD, and James
South, MA

ABSTRACT:
Mild silver protein has been used since the 19th century as an
antimicrobial agent, with a wide range of bactericidal, fungicidal,
and virucidal properties. This paper reviews the historical use of
mild silver protein in medicine, and documents the recent
effectiveness of intravenous mild silver protein to cause a dramatic
reduction in viral load of 3 patients with human immunodeficiency
virus.
(Clinical Practice of Alternative Medicine 2(1):48-53, 2001)


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CSArgyria treatment

2002-04-18 Thread I Anderson

I agree with James,

that the first port of call if one suspects Argyria is confirmation
via tissue biopsy. Only then can one be sure that the correct
questions are being asked.

Ivan.


http://www.silverprotects.com/argyria.html

A Possible Cure for Argyria

Is it possible that restoring healthful levels of vitamin E and
selenium along with the ingestion of ample water might bring about a
gradual reversal of argyria in at least some cases? I decided to
discuss my idea with a nutritional specialist, Hans Gr uenn, MD. After
talking at length about the EPA studies and the properties of vitamin
E and selenium, Dr. Gruenn concluded, It is a worthy hypothesis that
should be tried. Dr. Gruenn gave the following recommendations:


200mcg to 400mcg of selenium per day is a safe supplement to take on
an ongoing basis.
He also advises a high-quality,* mixed vitamin E, at 1000 IU per day
for people over 50 years of age who may be at risk of stroke, and
2,000 IU per day for people under 50 who are not at risk of stroke. I
told Dr. Gruenn that I was taking 4,000 IU a day. He replied that this
was still safe for a strong healthy person. The danger of high doses
of vitamin E is that it thins the blood. This could be dangerous in
many situations where bleeding is hard to stop.
Personally, I would also drink lots of water, simply because that's
how the body clears out debris. No one knows if this therapy will
prove efficacious, or if it does in how many cases. If my liver spots
are any kind of indicator, some lightening of t he skin ought to be
visible within six weeks if this therapy really is working. Three to
six months should be a sufficient amount of time to completely
eliminate argyria provided that no additional silver is being
ingested. (Since my conversation with Dr. Gruenn, I've had some
additional ideas for getting the most out of this nutritional therapy
for argyria.)
2 tsp. of MSM per day. Sulfur (MSM) binds with silver and can help to
pull it from the body. More information on silver and sulfur can be
found on page 88.
4,000 mg. of vitamin C per day.
1 tablet a day of a good quality multiple mineral since this therapy
may deplete needed minerals from the body.
* Most vitamin E supplements are of poor quality and some even contain
rancid oils that will be an additional burden rather than an aid to
the body. Dr. Gruenn recommends a vitamin E that has a mix of d-alpha,
beta, delta and gamma tocopheryls


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RE: CSColloidal vs silver ions

2002-04-18 Thread I Anderson
Well, I was bound to comment on the ionic vs elemental colloid thread
eventually...

Firstly the idea that silver ions precipitate out in the elementary
tract, and never make it to the blood stream, is pure speculation.
This theory is most eloquently proposed by Purest Colloids who market
a product of high elemental colloid percentage.

However the theory, I believe, is pretty much debunked by an article
which is (ironically) found on the Purest Colloids sister web site:
http://www.silver-colloids.com/Papers/AltmanStudy.PDF

This study was written by Roger Altman (who used to grace this list
with his not inconsiderable presence) and details the elimination vs
ingestion of what would be a high ionic percentage CS. He found that
pretty much what is ingested is what comes out, and that a high
percentage comes out in the urine. Now these ions did not get into the
urine by precipitating out and not getting into the blood stream,
obviously the blood stream is exactly where they ended up.

The fact that a high percentage of ingested ions emerged in the urine
also suggests that little is bound in the tissues (at least in this
case) which further suggests that in order to develop argyria, a large
amount of silver must be consumed, and/or specific (and unusual?)
circumstances are present, such as deficiencies in vitamin E and/or
selenium (or perhaps overdose of selenium, as suggested by some
research).

What the fate of silver ions in the blood before elimination is moot,
however my own observations would suggest that they are at least as
effective as elemental colloids in controlling infection... so don't
throw away your 9v battery generator just yet!

Ivan.


 -Original Message-
 From: Marshall Dudley [mailto:mdud...@execonn.com]
 Sent: Tuesday, 16 April 2002 9:06 a.m.
 To: silver-list@eskimo.com
 Subject: Re: CSColloidal vs silver ions


 While it is the ionic form that can cause argyria, there is a
 minimum amount of
 silver necessary.  According to I believe it is, the EPA
 website, one would have
 to drink so much 5 ppm CS 90% ion they would die from water
 poisoning first.

 It helps to understand what is going on here.

 1. Silver ions will combine with the hcl in the stomach and
 mostly precipitate
 out as silver chloride.  Thus they never make it to the blood
stream.
 2. In the body, silver ions can precipitate out onto silver
 particles when a
 developer such as caffine is present.  When taking silver
 salts, there are no
 particles, but particles are formed when the salts are
 exposed to light.  Thus
 when taking silver salts, the initial particles will always
 occur in skin
 exposed to light.  At that point, the ions in the salts can
 precipitate out onto
 the particles and thus make them grow until they become bound
 in the tissue
 making what is basically a tatoo.
 3. Silver salts must be present in a large enough quantity so
 that particles
 grow rapidly enough to become lodged before being flushed
 out.  This requires a
 fairly high concentration of silver ions in the blood.

 So we have 3 reasons why normal CS should not be a problem.
 Most of the ions
 combine with chlorine and precipitate out, those that do make
 it to the blood
 stream will bind with silver particles throughout the body,
 instead of just in
 the skin, the concentration of ions will be too low to cause
 significant
 particle size increase and lodging.

 Marshall

 Bobbye Stegen wrote:

  Hi all,
 
  I am a novice in the world of colloidal silver.  I have
 attempted to read up
  on using the product, asking questions, etc.  I've read the
 Purest Colloids
  web site which holds the patent on the process of a higher
 % of colloidal
  particulate matter.  The web site is impressive but alas,
 the product is
  very expensive.
 
  I have read many of your messages discussing making your
 own CS and on other
  boards/lists.
  Now as I understand it, the CS you make at home has a high
 percentage of
  silver ions  Now if I understand it correctly, it is the
 ionic silver that
  can cause the blue discoloration.
 
  At this point, I don't want to even attempt to make my own
 CS as I want to
  experiment to see if  CS works for me and my family as many
 of you have
  attested to.
 
  My question is, if ionic silver can cause a problem no
 matter how small a
  chance, why would you take a chance making your own?  This is not
a
  challenging question but request for information only.
 
  CS costing $61 a bottle is still much much cheaper and
 better for the
  bodyespecially if one does not use allopathic medicines
 unless it is a
  matter of life and death.
 
  I've looked at the health food stores and find 10ppm and
 30ppm on the
  shelves.  Now is this ionic silver?  If you were going to
 buy CS, would you
  risk buying anyother on the market other than the Purest
 Colloids?  Have any
  of you tried Purest Colloids?
 
  Again, this is not to start a debate but just asking for
 honest opinions.
 
  Thanks,
 
  Bobbye
 
  --
  

RE: CSH2O2 in CS

2002-04-14 Thread I Anderson
Bob,
I think you will find that USP stands for US Pharmacopeia, which is a
set of standards and processes that must be followed in order to use
the label. USP relates to purity only so far as is laid out in the
standard.

Ivan.



-Original Message-
From: Bob Bartell [mailto:bobbart...@earthlink.net]
Sent: Monday, 15 April 2002 9:09 a.m.
To: silver-list@eskimo.com
Subject: RE: CSH2O2 in CS


Thanks Kevin.   Still think its wrong to use USP to ascribe  a level
of purity when the product contains identifiable other components -
trace amounts or otherwise.   Namaste:  Bob Bartell




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RE: CSVirgin Coconut oil vs. Copra

2002-04-10 Thread I Anderson
Dear Catherine,

Thanks, but this page says nothing about coconut milk or cream. The
fact is that coconut milk and cream supply appreciable amounts of
short chain fatty acids, which are the active ingredients of CNO. One
does well to eat them. Even macaroons are said to be of benefit by
coconut oil guru Mary Enig.

Ivan.


 -Original Message-
 From: Catherine Creel [mailto:ccr...@maine.rr.com]
 Sent: Wednesday, 10 April 2002 5:55 p.m.
 To: silver-list@eskimo.com
 Subject: CSVirgin Coconut oil vs. Copra


 What is Virgin Coconut Oil?
 Virgin Coconut Oil can only be achieved by using fresh
 coconut meat or what
 is called non-copra (see below for a definition of copra).
 Chemicals and
 high heating are not used in further refining. There are
 currently two main
 processes of manufacturing Virgin Coconut Oil:

 1. Quick drying of fresh coconut meat which is then used to
 press out the
 oil. Using this method, minimal heat is used to quick dry the
 coconut meat,
 and the oil is then pressed out via mechanical means.

 2. Wet-milling. With this method the oil is extracted from
 fresh coconut
 meat without drying first. Coconut milk is expressed first
 by pressing.
 The oil is then further separated from the water. Methods
 which can be used
 to separate the oil from the water include boiling, fermentation,
 refrigeration, enzymes and mechanical centrifuge.

 The method which is used by Mt. Banahaw Health Products
 Corporation in the
 Philippines is fermentation. The coconut milk expressed from
 the freshly
 harvested coconuts is fermented for approximately 48 hours.
 During this
 time, the water separates from the oil. The oil is then
 slightly heated for
 a short time to remove moisture, and filtered. The result is
 a clear coconut
 oil that retains the distinct scent and taste of coconuts. This is a
 traditional method of coconut oil extraction that has been used in
the
 Philippines for hundreds of years. Laboratory tests show that
 this is a very
 high quality coconut oil, with the lauric acid content often
 being over 53%.
 This oil is not mass produced, but made by hand just as it
 has been done for
 hundreds of years. Since we live in the community where the
 coconuts grow,
 we personally guarantee that the best organic coconuts
 available are used in
 producing this Virgin Coconut Oil, and that no chemicals
 whatsoever are used
 in the growing or processing of the coconuts.

 How is Virgin Coconut Oil different from other coconut oils?

 Most commercial grade coconut oils are made from copra. Copra
 is basically
 the dried kernel (meat) of the coconut. It can be made by:
 smoke drying, sun
 drying, or kiln drying , or derivatives or a combination of
 these three. If
 standard copra is used as a starting material, the unrefined
 coconut oil
 extracted from copra is not suitable for consumption and must
 be purified,
 that is refined. The standard end product made from copra is
 RBD coconut
 oil. RBD stands for refined, bleached, and deodorized. Both
 high heat and
 chemicals (e.g. solvent extractions) are used in this method.

 RBD oil is also often hydrogenated or partially hydrogenated.
 Hydrogenated
 oils have been shown to increase serum cholesterol levels
 which contribute
 to heart disease.

 http://www.tropicaltraditions.com/what_is_virgin_coconut_oil.htm




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RE: CSRe: CS TASTE POLL -- The 3 Questions

2002-04-10 Thread I Anderson
Just to add another ingredient into the stew...
I had a reference about two hard drives ago, which advanced the idea
that people who experience strong metallic taste do so because of the
presence of sulphur bearing (producing?) bacteria at the base of the
tongue and throat.

Ions should taste stronger than metals because they can interact with
the taste buds more readily.

Ivan.



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RE: CSPriorities (coconut oil)

2002-04-09 Thread I Anderson
Nothing wrong with copra Tracy,
Its dried coconut meat. Passing water through desiccated coconut and
pressing it out is the only way I know of to obtain coconut milk.
Coconut milk is the next best thing to coconut oil, as it contains up
to 20% (by memory) oil, assuming its a good brand. If it goes hard in
the fridge it probably contains appreciable amounts of oil.

Ivan.

 -Original Message-
 From: Nick Grant [mailto:nwgr...@inet.net.nz]
 Sent: Tuesday, 9 April 2002 10:04 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CSPriorities (coconut oil)


 That sounds ominous.  Copra.  Has a nasty ring...:)  What is it?

 Tracy


 - Original Message -
 From: Catherine Creel ccr...@maine.rr.com
 To: silver-list@eskimo.com
 Sent: Tuesday, 9 April 2002 19:46
 Subject: Re: CSPriorities (coconut oil)


  Hi Tracy,
 
  The brand is Trident, and it is not sweetened, or
 homogenised.  Just
  coconut
  and water and a preservative of course.
 
 
  Good!  But the preservative...oy vey.  Also, you may
 want to ask the
  company
  how it's processed.  My understanding is most companies use copra.
 
  Catherine


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RE: CSCancer: cause and cure

2002-04-09 Thread I Anderson

Jason,
I am not quite sure what you are trying to say in your message.
Individual cancers cases are to be treated on their particular
circumstances of course, and I did say that the internal 'landscape'
needs to be altered for lasting results, and that this MAY be
sufficient in and of itself. Does that make me an honest (I already
know I'm not a cancer expert)?
Being a vegetarian generally means that one does not have the optimum
balance of minerals and vitamins, or protein to carbohydrate intake,
and the intake of saturated fats is likely to be less than ideal. How
much vitamin D is in the diet, how much calcium is being absorbed...
there are endless questions to be answered before one can gain an idea
of how a person had become susceptible to cancer, and how best to
treat it.
I'm sorry to hear that this person has joined the legion for whom
treatment failed, and I guess she was poorly advised and made the
wrong choices. But all is not lost (I hope) and with proper guidance,
she may yet triumph.

As to DNA repair and life extension, I'm for it!
Of course, optimal cell function, I'm sure you would agree, begins
with optimal nutrient balance.

Be well!
Ivan.

 -Original Message-
 From: AVRA / Jason [mailto:silverd...@hotmail.com]
 Sent: Tuesday, 9 April 2002 2:16 a.m.
 To: *Silver-List* (E-mail)
 Subject: Re: CSCancer: cause and cure


 Ivan:

 Point and case is a very virulent basil cell cancer I've just
 been made
 aware of.  The individual has been on a strict alkaline diet
 now for a long
 time, and has been given a death sentance by the Mao Clinic.
 The individual
 is a vegetarian as well.  The change in the alkaline
 conditions of the body
 have done absolutely nothing to slow the cancer growth.
 While this may
 surprise others, it doesn't surprise me.  I haven't met an
 honest cancer
 expert that doesn't agree with the idea that a body alkaline
 environment
 isn't always enough.

 DNA repair is absolutely critical in another arena of research, life
 extension...  I agree that as far as cancer is concerned, the
 direct repair
 of DNA is really not ideal.  But when one is talking about
 accelerating cell
 functions, it is critical that one begins with optimally
 functioning cells.

 Needless to say, it really pisses me off that places like the
 Mayo clinic
 are trashing people's lives.  It further upsets me that any
 treatment is
 touted as the cure, which leads the individual to stop
 seeking a solution,
 thinking that what they are doing is enough.  This individual
 has lost an
 eye, and may lose another, because the cancer has not responded to
 treatment, and is now fully inoperable.  None of all of that
 was necessary.

 Jason

 - Original Message -
 From: I Anderson i...@win.co.nz
 To: silver-list@eskimo.com
 Sent: Monday, April 08, 2002 4:55 AM
 Subject: RE: CSCancer: cause and cure


  Jason,
 
  There is no point in attempting to repair mutated DNA, in
 my opinion.
  When a healthy cell develops a problem the cell self destructs,
this
  does not happen in cancer cells and so they continue to
 grow. Best to
  kill them off. Some treatments such as polyMVA do work directly
with
  the DNA, often allowing the cell to go into apoptosis (self
  destruction).
 
  The prime causes of cancers are many and varied, but the process
is
  the same in them all. A pH of 7.4 in all fluids and tissue, except
  urine and stomach, with the proper calcium reserves, create
 conditions
  which make it difficult for even the worst carcinogens to gain
entry
  to the cell.
 
  The central problem is an internal landscape which is
 chemically, and
  therefore electrically, unable to defend against mutagens. Such an
  internal chemistry begets an impaired immune system which
 is unable to
  repair the defects caused by ionising radiation for instance.
 
  I am sure that various electrical or EMF devices can cause an
immune
  or physiological response, just as IR light, or sound can. Even
  colours or essential oils have this property, as does acupuncture
or
  meditation or the laying on of hands.
 
  But the bottom line is that the internal landscape needs
adjustment
  for lasting results and may be sufficient in and of itself.
 
  Regards
  Ivan
 
   -Original Message-
   From: AVRA / Jason [mailto:silverd...@hotmail.com]
   Sent: Monday, 8 April 2002 5:43 p.m.
   To: silver-list@eskimo.com
   Subject: Re: CSCancer: cause and cure
  
  
   Kevin:
  
   I agree with your thinking.  When one central cause for
   something is usually
   found, then one central cure usually suffices; vitamic C always
  cures
   Scurvy.
  
   That is why my primary and fundamental method of
 treatment is based
  in
   natural medicine. Oxygen treatments don't always work, that
   is for certain.
   You move the body toward a state of improved health, while
  addressing
   identifiable and treatable conditions directly.
  
   I believe the oxygen issue is a symptom of a cause, not a
   cause.  I believe
   the PH

RE: CSCitric Acid and CS

2002-04-09 Thread I Anderson
Kathie,
Vitamin C has the habit of gobbling up metals, which would tend to
render both useless. So probably best to separate the intake.

Ivan.

-Original Message-
From: Kathie Jones [mailto:kathiejo...@comcast.net]
Sent: Tuesday, 9 April 2002 2:58 a.m.
To: silver-list@eskimo.com
Subject: CSCitric Acid and CS


 Has  anyone read/heard/etc anything about the presence of CS and
a citric based drink or food a non-no at the time of oral ingestion of
CS? I read such about a year ago and since then we have been careful
about ingesting CS with orange juice, vitamin C, etc since then.

Thought? Insights?

Kathie


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RE: CSUnidentified subject!

2002-04-09 Thread I Anderson
Thanks Ronan,

Yes it seems that the negative pole of a magnet will cause the body
fluids to become more alkaline. Calcium bicarbonate, normally a
straight molecule, will bend and break into calcium hydroxide and CO2.

The cytoplasm oscillates between pH 7.4 and 6.6 as the pores open and
close and cations and nutrients enter and leave the cell.

Thanks for the input... and I must say that I am seriously considering
purchasing a magnetic bed underlay... what do you think?

Ivan.

 -Original Message-
 From: Ronen Yehiav [mailto:y...@bezeqint.net]
 Sent: Tuesday, 9 April 2002 4:33 a.m.
 To: *Silver-List* (E-mail)
 Subject: Re: CSUnidentified subject!



 - Original Message -
 From: I Anderson i...@win.co.nz
 Subject: RE: CSUnidentified subject!


  Hi Terry,
 
  confirm in the most, what I have learned. What does seem to
 be missing
  is the recognition of the manner in which calcium becomes
  bio-available. Most diseased states benefit from an
 increase in serum
  calcium levels, it is the most needed of all minerals and
 is involved
  to some extent in every bodily process, so I guess it is
surprising
  that it is one of the hardest to absorb by modern man. The
  requirements for the absorption of calcium are that it is ionised
  (dissolved) and that the vitamin D receptors in the small
intestinal
  wall are populated with vitamin D. In these times of little sun
  exposure, and sun blocks, one needs to supplement with vitamin D
if
  one wishes to absorb 20 times more calcium than one would
otherwise.
 
  To my mind it doesn't much matter which type of calcium one
 takes, if
  one remembers that calcium will form insoluble compounds with
  phosphorous, and it is advantageous to take malic acid in
 the form of
  apple juice which will keep the calcium ionised long enough for
good
  absorption. The idea that two different types of calcium will
react
  together to supply useable energy I find suspect, especially
  considering that this will take place in the stomach.

 Up to this point, I agree completely:

 The ONLY variable I found which consistently affects calcium
 absorption is
 cellular metabolism.  This primary life - force process has a direct
 relation to the cellular magnetic charge, which must be
 negative.  This is,
 BTW, an alkaline state of the cytoplasm.

 Any other state of charge disrupts cellular metabolism.  When
 this happens,
 calcium absorption is not the only thing that goes wrong.

 The easiest, most consistent way I found to help the body
 recharge itself is
 through day - time charging of the sternum point with a
 powerful negative
 pole of a permanent magnet.

 If the body has a significant load of parasites, Zapping may help.

 I get magnets from www.magnetizer.com (they also have a very
 educational
 book),
 and I get zappers from www.worldwithoutparasites.org which I
 found to be the
 best there are, for several reasons.

 Ronen.


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RE: CSPriorities (coconut oil)

2002-04-09 Thread I Anderson
   Read here:

 www.coconut-info.com

   Copra has lost the benefits of the coconut.

 Catherine

No it hasn't. Here are a couple of links found at www.coconut-info.com
as suggested.

http://www.apcc.org.sg/special.htm
Earlier this year, at a special conference entitled, Functional Foods
For Health Promotion: Physiologic Considerations; EXPERIMENTAL
BIOLOGY '99, Renaissance Washington Hotel, Washington, DC Saturday,
April 17, 1999, which was sponsored by the International Life Sciences
Institute, ILSI NORTH AMERICA, Technical Committee on Food Components
for Health Promotion, the term functional foods was defined as  a
functional food provides a health benefit over and beyond the basic
nutrients.
This is exactly what coconut and its edible products such as
desiccated coconut and coconut oil do.  As a functional food, coconut
has fatty acids that provide both energy (nutrients) and raw material
for antimicrobial fatty acids and monoglycerides (functional
components) when it is eaten.  Desiccated coconut is about 69% coconut
fat, as is creamed coconut.  Full coconut milk is approximately 24%
fat.

http://www.coconut-info.com/weight-loss.htm
The second thing you should do is use other coconut products as much
as possible. Find ways to use fresh and dried coconut. You can find
recipes in cookbooks. Coconut milk is a wonderful item that can be
used in a wide variety of dishes. It can replace cowÂ’s milk and cream
in most any recipe and tastes great. Some of the dishes I make using
coconut milk include butterscotch pudding, coconut milk pancakes, clam
chowder, chicken almondine, and creamy coconut gravy, to mention just
a few. Coconut milk that you buy in the can is not sweetened so it can
be used for a wide variety of main dishes or desserts. With delicious
meals like these, dieting can be a pleasure, and because there are no
calorie restrictions to worry about, it can easily be maintained for
life without feeling hungry or deprived.

When combined with a high-fiber diet, using coconut oil and coconut
products can have a remarkable effect on your weight and your health.
For more detailed information about using coconut products to lose
unwanted weight I recommend the book Eat Fat, Look Thin: A Safe and
Natural Way to Lose Weight Permanently. This book outlines a dietary
program based on coconut and includes numerous delicious recipe

The second thing you should do is use other coconut products as much
as possible. Find ways to use fresh and dried coconut. You can find
recipes in cookbooks. Coconut milk is a wonderful item that can be
used in a wide variety of dishes. It can replace cowÂ’s milk and cream
in most any recipe and tastes great. Some of the dishes I make using
coconut milk include butterscotch pudding, coconut milk pancakes, clam
chowder, chicken almondine, and creamy coconut gravy, to mention just
a few. Coconut milk that you buy in the can is not sweetened so it can
be used for a wide variety of main dishes or desserts. With delicious
meals like these, dieting can be a pleasure, and because there are no
calorie restrictions to worry about, it can easily be maintained for
life without feeling hungry or deprived.

When combined with a high-fiber diet, using coconut oil and coconut
products can have a remarkable effect on your weight and your health.
For more detailed information about using coconut products to lose
unwanted weight I recommend the book Eat Fat, Look Thin: A Safe and
Natural Way to Lose Weight Permanently. This book outlines a dietary
program based on coconut and includes numerous delicious recipe

Ivan.



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RE: CSPriorities (coconut oil)

2002-04-09 Thread I Anderson
No, you were drinking coconut water. Pretty good for you too. The best
sports drink never manufactured.

Ivan.

 -Original Message-
 From: Marshall Dudley [mailto:mdud...@execonn.com]
 Sent: Wednesday, 10 April 2002 2:45 a.m.
 To: *Silver-List* (E-mail)
 Subject: Re: CSPriorities (coconut oil)


 I thought coconut milk was the liquid inside of a coconut.
 Broke a coconut
 last week and drunk some myself.

 Marshall



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RE: CSUnidentified subject!

2002-04-08 Thread I Anderson
Hi Terry,

I read your message with interest.. I have found Reams' theories to be
a very difficult to critique mainly because he invented his own
scientific jargon. However, his treatments appear to be valid and
confirm in the most, what I have learned. What does seem to be missing
is the recognition of the manner in which calcium becomes
bio-available. Most diseased states benefit from an increase in serum
calcium levels, it is the most needed of all minerals and is involved
to some extent in every bodily process, so I guess it is surprising
that it is one of the hardest to absorb by modern man. The
requirements for the absorption of calcium are that it is ionised
(dissolved) and that the vitamin D receptors in the small intestinal
wall are populated with vitamin D. In these times of little sun
exposure, and sun blocks, one needs to supplement with vitamin D if
one wishes to absorb 20 times more calcium than one would otherwise.

To my mind it doesn't much matter which type of calcium one takes, if
one remembers that calcium will form insoluble compounds with
phosphorous, and it is advantageous to take malic acid in the form of
apple juice which will keep the calcium ionised long enough for good
absorption. The idea that two different types of calcium will react
together to supply useable energy I find suspect, especially
considering that this will take place in the stomach.

Once in the body calcium is transported into the blood by
calcium-binding proteins which are stimulated by vitamin D, and from
the blood the deposition in the bones is controlled by the calcitonin
hormone released from the parathyroid gland. Calcitonin, along with
inositol triphosphate control both the deposition and removal of
calcium from the cells. The parathyroid glands are controlled by the
pituitary gland, which lies behind the eyes, and is stimulated by FULL
spectrum light, whilst inositol triphosphate is stimulated by cellular
photoreceptors.
So it can be seen that sunlight is a basic need for proper bodily
function and instrumental in the absorption and distribution of the
most important body constituent, calcium.

Regards
Ivan.

 -Original Message-
 From: Terry Chamberlin [mailto:tcj...@yahoo.ca]
 Sent: Monday, 8 April 2002 7:48 a.m.
 To: silver-list@eskimo.com
 Subject: CSUnidentified subject!


 I was wondering why there is such a difference
 between ones Urine PH, and Ones Saliva PH. Also, which
 one would give a correct indication of the body's
 Alkaline/Acid content..   Thanks, Grant..

 The following is to address the pH issue, from the
 literature I give to all my clients. It is intended
 here for informational purposes, not as a marketing
 ploy.

 The Calcium Connection
 Determining which calcium your body needs

 Nowadays there is a lot of talk about our need for
 calcium. You will see products from milk to orange
 juice with the words Calcium Added! prominently
 displayed on the label. Nearly everyone knows how a
 lack of calcium can contribute to such health issues
 as arthritis and osteoporosis. Nearly everyone also
 knows that calcium levels have decreased significantly
 in our modern food, which is commercially grown in
 mineral-poor soil. To get enough calcium, most people
 recognize the need to take calcium supplements.

 But when you go to the pharmacy or a health food
 store, it can become confusing. You see all kinds of
 calciums. There is calcium carbonate, lactate, citrate
 and gluconate, which are on almost every shelf. Then
 there are the less well-known calciums such as calcium
 phosphate, sulphate, aspartate, orotate, hydroxide,
 plus others with names too difficult to pronounce!

 It makes you wonder: Are some kinds of calcium better
 than others? Does it matter which kind of calcium you
 take? Is it possible to take too much calcium? Can
 calcium hurt you? Do the various kinds of calcium
 affect the body in different ways?

 According to the late Dr. Carey Reams, bio-chemist and
 bio-physicist, our bodies need a balanced variety of
 calciums. He spent over 50 years studying and
 researching the affects of various calciums and other
 minerals on the human body. He found that there are
 essentially three categories of calciums to be
 considered: Alkaline-pH calciums (calcium hydroxide,
 phosphate and carbonate), Acid-pH calciums (calcium
 lactate and sulphate) and neutral-pH calciums (calcium
 citrate, aspartate, gluconate, etc.). pH, as used
 here, refers to the  acidifying or alkalinizing effect
 upon the body.

 The body needs calcium from each of these groups in
 order to achieve balance for good health. Frequently
 people have an adequate amount of one kind, but a
 deficiency of the other. The presence of both
 acidifying and alkalinizing calciums is important
 because the interaction between the two is how both
 kinds are assimilated. Without enough of one kind,
 there is a poor assimilation of the other.

 Imagine taking a cup of vinegar and a cup of baking
 soda. If you dump 

RE: CSSilver Compounds and electrobiological/electromagnetic response

2002-04-08 Thread I Anderson
Hi Kevin,

Yes both high and low pH will kill cancer cells, indeed cancer cells
kill themselves by producing large quantities of lactic acid. The acid
drops the pH to a point where the cell can no longer function. A
cancer mass is a core of dead cells surrounded by a skin of actively
growing cancerous tissue... it is not the mass itself which kills the
host, but the toxins leaking from the dead centre.
Cesium or rhodium salts by their physical nature are able to enter
cancer cells but are unable to get out, and being the most alkaline of
all metals will raise the pH to a level which also kills the cancer,
neutralising the acidic toxins as they go. This is called High pH
Therapy and is something that I offer to people who ask me for help.

Manfred von Ardennene, of Otto Warburg's students advances a therapy
which relies on the massive uptake and use glucose to feed cancer
cells, thus lowering their pH:

In Europe, the sugar feeds cancer concept is so well accepted that
oncologists, or cancer doctors, use the Systemic Cancer Multistep
Therapy (SCMT) protocol. Conceived by Manfred von Ardenne in Germany
in 1965, SCMT entails injecting patients with glucose to increase
blood-glucose concentrations. This lowers pH values in cancer tissues
via lactic acid formation. In turn, this intensifies the thermal
sensitivity of the malignant tumors and also induces rapid growth of
the cancer. Patients are then given whole-body hyperthermia (42 C core
temperature) to further stress the cancer cells, followed by
chemotherapy or radiation.19 SCMT was tested on 103 patients with
metastasized cancer or recurrent primary tumors in a clinical phase-I
study at the Von Ardenne Institute of Applied Medical Research in
Dresden, Germany. Five-year survival rates in SCMT-treated patients
increased by 25 to 50 percent, and the complete rate of tumor
regression increased by 30 to 50 percent.20 The protocol induces rapid
growth of the cancer, then treats the tumor with toxic therapies for a
dramatic improvement in outcome.

The irrefutable role of glucose in the growth and metastasis of cancer
cells can enhance many therapies. Some of these include diets designed
with the glycemic index in mind to regulate increases in blood
glucose, hence selectively starving the cancer cells; low-glucose TPN
solutions; avocado extract to inhibit glucose uptake in cancer cells;
hydrazine sulfate to inhibit gluconeogenesis in cancer cells; and
SCMT
http://www.mercola.com/article/sugar/sugar_cancer.htm

As Terry
 Chamberlain has
 pointed out, too high a pH is associated with poor digestion,
 constipation
 etc. This creates a dilemna for anyone already experiencing
 those symptoms
 (I have on and off) who wants to guard against cancer. A
 naturopath friends
 advice to acidify my system by taking lots of lemon juice,
 and for a while
 calcium lactate, certainly fixed up a bout of constipation

Well that may be correct, but it has to be pretty difficult to be too
alkaline, unless one is a strict vegetarian, or is taking large doses
of alkaline salts. Lemon juice is ultimately alkaline forming as is
calcium, the lactates are well tolerated by all except those with low
pH. You may have been calcium deficient.

Glad your on the move now though.

Ivan.

 -Original Message-
 From: Kevin Nolan [mailto:ken...@optusnet.com.au]
 Sent: Monday, 8 April 2002 1:54 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CSSilver Compounds and
electrobiological/electromagnetic
 response


 Thanks Ivan. As you say, a big question. Low cellur pH then
 seems to be a
 chief cause of cancer initiation. Does that mean that raising
 cellular pH
 will reverse the process once cancer has set in? As Terry
 Chamberlain has
 pointed out, too high a pH is associated with poor digestion,
 constipation
 etc. This creates a dilemna for anyone already experiencing
 those symptoms
 (I have on and off) who wants to guard against cancer. A
 naturopath friends
 advice to acidify my system by taking lots of lemon juice,
 and for a while
 calcium lactate, certainly fixed up a bout of constipation.

 regards, Kevin Nolan

 - Original Message -
 From: I Anderson i...@win.co.nz
 To: silver-list@eskimo.com
 Sent: Sunday, April 07, 2002 10:09 PM
 Subject: RE: CSSilver Compounds and
electrobiological/electromagnetic
 response


  Hi Kevin,
  You ask a BIG question, which requires time to marshal a response.
 
   Does anaerobic metabolism cause cancer?
 
  Warburg had quite a bit to say about oxygen and cancer, but I am
not
  sure that he gave an answer to that question. What he did find in
  cancerous tissue was impaired or defective mitochondrial
 processes. It
  is in the mitochondria that cellular energy processes
 occur, normally
  by the oxidation of glucose with the products being ATP, CO2 and
  water. The process proceeds through a glycolysis phase
 which produces
  a small amount of ATP and lactic acid. The lactic acid would then
be
  oxidised further with a much larger production

RE: CSPriorities

2002-04-08 Thread I Anderson
The anti-microbial action of pure virgin coconut oil is but a bonus to
its real benefits. The fact that CNO is a saturated short chain fat
means that it normalises cholesterol levels, does not deplete the
bodies reserves of antioxidants as do polyunsaturated fats, does not
form toxic trans-fatty acids, is protective of the heart, liver and
vascular systems, increases metabolism, causes weight loss and so on.
It is the healthiest of all the fats.

Regards
Ivan.

 -Original Message-
 From: Russ Rosser [mailto:russros...@rovin.net]
 Sent: Monday, 8 April 2002 2:02 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CSPriorities

 Raw coconut oil?  There was a HUGE thread about coconut's
 anti-microbial
 properties some time ago.  The lists harps on saturated
 fat.  Cancer was
 unknown among Eskimos whie their diet was up to 90% fat, in
 the form of RAW
 whale blubber, etc.  Even the word eskimo means 'eats it raw.'

 --Russ


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RE: CSCancer: cause and cure

2002-04-08 Thread I Anderson
Jason,

There is no point in attempting to repair mutated DNA, in my opinion.
When a healthy cell develops a problem the cell self destructs, this
does not happen in cancer cells and so they continue to grow. Best to
kill them off. Some treatments such as polyMVA do work directly with
the DNA, often allowing the cell to go into apoptosis (self
destruction).

The prime causes of cancers are many and varied, but the process is
the same in them all. A pH of 7.4 in all fluids and tissue, except
urine and stomach, with the proper calcium reserves, create conditions
which make it difficult for even the worst carcinogens to gain entry
to the cell.

The central problem is an internal landscape which is chemically, and
therefore electrically, unable to defend against mutagens. Such an
internal chemistry begets an impaired immune system which is unable to
repair the defects caused by ionising radiation for instance.

I am sure that various electrical or EMF devices can cause an immune
or physiological response, just as IR light, or sound can. Even
colours or essential oils have this property, as does acupuncture or
meditation or the laying on of hands.

But the bottom line is that the internal landscape needs adjustment
for lasting results and may be sufficient in and of itself.

Regards
Ivan

 -Original Message-
 From: AVRA / Jason [mailto:silverd...@hotmail.com]
 Sent: Monday, 8 April 2002 5:43 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CSCancer: cause and cure


 Kevin:

 I agree with your thinking.  When one central cause for
 something is usually
 found, then one central cure usually suffices; vitamic C always
cures
 Scurvy.

 That is why my primary and fundamental method of treatment is based
in
 natural medicine. Oxygen treatments don't always work, that
 is for certain.
 You move the body toward a state of improved health, while
addressing
 identifiable and treatable conditions directly.

 I believe the oxygen issue is a symptom of a cause, not a
 cause.  I believe
 the PH issue can be both a symtpom and a cause.  I believe
 the DNA issue can
 be a symptom and a cause.  Solvents and other chemicals in
 the body can be a
 cause.  Radiation can be a cause.  Deficiencies can be a cause.
 Electromagnetic pollution can be a cause.

 In all of my experience with cancers, the one central theme I
 have noticed
 is that all cancer has been demonstrated ( to me ) to be an
 immune system
 deficiency.  I've heard it said that cancer can be an immune system
 over-response, but this is not my experience.

 Dr. Robert O. Beck's research makes the most sense to me, as his
 observations fit soundly with all the symptoms and causes of
 cancer that I
 am aware of.  The central problem is cell differentiation,
 the causes are
 multitudinous.

 If it is a DNA problem, then the cancer will have to be
 destroyed, or the
 DNA repair mechanisms corrected.  If the DNA is shortened,
 how are any of
 these so-called cancer cures going to affect an absolute
 change, without
 eliminating the cells?  The answer is that they aren't.  The
 individual is
 going to die, despite internet websites touting six hundred
 thousand cancer
 cures.  There are very few researchers capable of direct DNA
 repair.  What
 about modified DNA?  Oxygen therapy isn't going to correct
 this, neither is
 a proper PH balance.  The cancer is going to create the
 conditions that
 promotes its own survival, and it is VERY capable of doing
 so, as it is a
 primitive cell structure.  The body is not going to recognize
 the cancer as
 an invasive agent.  The dead person won't be able to tell the
 world of all
 the failed alt cancer cures tried, and the families are usually to
 embarrased to speak out.

 The ongoing DNA repair work, on many levels, shows extreme
 promise.  The
 methods are through scalar wave technology and other
multi-dimensional
 energy approaches.  I'm involved in some aspects of this type
 of research,
 which is still years away from true practical application.
 Sonic waveforms
 show great promise.  The problem is that the technology that
 can accurately
 measure subtle forms of energy is just now becoming readily
 available. The
 technology allowing complete measurement of DNA sequencing
 has also been
 slow to surface.  The problem here is that weapons
 applications has kept
 much of this technology non-commercial.  Since it costs hundreds of
 thousands of dollars just to obtain the basic equipment
 needed, independent
 research has been very slow due to a complete lack of funding
 outside of
 defense applications.  Those involved in such research
 applications ( myself
 included ) cannot share too much along these lines, because
 the hundreds of
 thousands of dollars in measurement equipment rapidly
 translates to millions
 of dollars in applications equipment...  If the primary
 interests are not
 protected, then there would be no research at all.  True,
 repeatable medical
 applications are still quite a ways off, at any rate.  But 

RE: CSSilver Compounds and electrobiological/electromagnetic response

2002-04-08 Thread I Anderson
Indeed,
But I was describing the Krebs cycle which takes place in the lumen of
the mitochondria and is about the production of adenosine triphosphate
(ATP) via firstly glycolysis and finally oxidation of lactic acid, the
product of the first stage. The second stage produces about 5 times
more ATP than the first. The ATP is then available as an energy source
for cellular function by reduction to the species you mention.

Regards
Ivan.

 -Original Message-
 From: Malcolm Stebbins [mailto:s...@asis.com]
 Sent: Monday, 8 April 2002 5:52 p.m.
 To: *Silver-List* (E-mail)
 Subject: Re: CSSilver Compounds and
electrobiological/electromagnetic
 response




 I Anderson wrote:

  Hi Kevin,
  You ask a BIG question, which requires time to marshal a response.
 
   Does anaerobic metabolism cause cancer?
 
   It
  is in the mitochondria that cellular energy processes
 occur, normally
  by the oxidation of glucose with the products being ATP, CO2 and
  water. The process proceeds through a glycolysis phase
 which produces
  a small amount of ATP and lactic acid. The lactic acid would then
be
  oxidised further with a much larger production of ATP, CO2
 and water.
  Warburg found that the second phase did not occur in cancer cells,

 Hi, don't mean to be picky but I thought the energy cycle
 went from the high
 energy compound adenosine triphosphate to the lower energy
 one, adenosine
 diphosphate, and sometimes further to adenosine
 monophosphate, or AMP; yes?
 Take care,  Malcolm


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RE: CSSilver Compounds and electrobiological/electromagnetic response

2002-04-07 Thread I Anderson
Hi Kevin,
You ask a BIG question, which requires time to marshal a response.

 Does anaerobic metabolism cause cancer?

Warburg had quite a bit to say about oxygen and cancer, but I am not
sure that he gave an answer to that question. What he did find in
cancerous tissue was impaired or defective mitochondrial processes. It
is in the mitochondria that cellular energy processes occur, normally
by the oxidation of glucose with the products being ATP, CO2 and
water. The process proceeds through a glycolysis phase which produces
a small amount of ATP and lactic acid. The lactic acid would then be
oxidised further with a much larger production of ATP, CO2 and water.
Warburg found that the second phase did not occur in cancer cells,
leading to the rise in concentration of lactic acid (and therefore
lowering of pH), and found that mitochondria was impaired in some way.
I think he believed that a lack of oxygen caused mitochondrial damage,
but others disagree, the fact remains, however, that where there is
lactic acid build there is anaerobic energy production, whether this
is in the presence of oxygen or not.

What causes a cell to become cancerous in the first place is the
mutation of dna (be it cellular or mitochondrial) or some impairment
of cellular process, notably the expression or manufacture of proteins
and enzymes, from nucleotide building blocks. A normal pH ensures the
breakdown glucose into the A, C, G and T nucleotide radicals that
promote healthy DNA synthesis, and severely limits the ability of
mutagens to cross the cellular membrane where they might cause some
mutation. If the extracellular plasma is more acidic than optimum the
intracellular fluid must also drop below normal (pH6.6) to maintain
the appropriate potential across the cellular membrane, not only does
this allow the passage of mutagens, but also impairs proper nucleotide
production. These events may cause cells to mis-function and develop
cancer. When the pH of a cancerous cell lowers sufficiently, the pores
on the cellular membrane do not work correctly (they are driven by
potential difference between the inside and the outside of the cell,
which is related to pH). This restricts the passage of oxygen but not
of glucose. So one can see a number of events which can lead to the
ceasing of oxidative respiration, leaving only glycolysis
(fermentation) as the source of energy for cancer cells.

The formation of cancerous tissue is not a function of available
oxygen per se, that is just a corollary of the process.
So does anaerobic respiration cause cancer..., no, anaerobic
respiration is a result of the physiological conditions that cancers
cause, ie, mitochondrial damage and disfucntional membrane pores by
way of low pH.

Regards
Ivan.



 -Original Message-
 From: Kevin Nolan [mailto:ken...@optusnet.com.au]
 Sent: Thursday, 4 April 2002 1:33 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CSSilver Compounds and
electrobiological/electromagnetic
 response


 The oft repeated claim from the alternative healing sector
 that cancer cells
 operate via a fermentation metabolism and thus are susceptible to
 oxygenation (Warburg hypothesis) is appealing and I hope true.
Stephen
 Barret of Quackwatch has justifiably received bad press here
 re CS safety.
 But that doesn't mean he gets it all wrong. On the matter of
 cancer cell
 metabolism, the following from
 http://www.quackwatch.com/01QuackeryRelatedTopics/Cancer/oxyge
 n.html is
 worth some serious pondering:

 Does anaerobic metabolism cause cancer?
 In a 1961 monograph [7], Aisenberg reviewed and analyzed the
 subject of
 energy metabolism in normal and tumor tissues. He concluded that
most
 carcinogens are not respiratory poisons; most respiratory
 poisons are not
 carcinogens; oxygen neither prevents nor inhibits cancer
 growth; tumor cells
 grow optimally in tissue culture dishes in atmosphere
 containing 20% oxygen;
 tumors grow rapidly in tissues that are well supplied with
 oxygenated blood;
 absence of oxygen does not stimulate tumor growth in vitro or in
vivo;
 agents effective against cancer interfere with DNA synthesis, not
with
 aerobic metabolism; tumors do not get a significant amount of
 their energy
 from anaerobic metabolism; tumors can and do produce energy by an
 oxygen-driven metabolism of fats and carbohydrates.

 Since the mid 1960s, information amassed has identified
 cancer initiation,
 promotion, and progression. Alteration of genetic regulation
 through DNA
 damage, oncogene activation, and inhibitor dysregulation give rise
to
 abnormally proliferating cancer cells. There is no evidence
 of poisoning
 in the respiratory enzyme systems of tumor tissues. Although Warburg
 discovered some differences in metabolism between normal and
 cancer cells,
 research did not bear out what he considered to be the
 primary cause of
 cancer, i.e., the replacement of respiration by fermentation.[7].

 Worth reading the rest of that article also. Comments anyone?

 Kevin 

RE: CSBody PH..

2002-04-07 Thread I Anderson
Grant,
The kidneys are part of the pH regulation system and will extract
hydrogen ions from the blood plasma in order to lower the plasma pH,
thus raising the pH of the urine accordingly. The saliva mirrors blood
pH, and while affected by food and may give false readings, it is
pretty accurate if one tests the saliva 3 hrs after putting anything
in the mouth, and draws two or three fresh lots into the mouth and
swallows it before testing. 11AM is a good time for doing this
according to Robert Barefoot, who also suggests repeating the
measurement on successive days and averaging the result.

Regards
Ivan.

 -Original Message-
 From: Grant [mailto:g...@island.net]
 Sent: Sunday, 7 April 2002 10:02 a.m.
 To: Silver - List
 Subject: CSBody PH..


 Hi there:

   I was wondering why there is such adifference between
 ones Urine PH,
 and Ones Saliva PH.. also which one would give a correct indication
of
 the bodys Alkaline/Acid content..

   Thanks  Grant..



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RE: CSSilver Compounds and electrobiological/electromagnetic response

2002-04-04 Thread I Anderson
Marlene'

1,3 1,6 beta glucans are natural sugars extracted from primarily yeast
cell walls, but are also found in oats, barley, mushrooms etc. They
work by stimulating and making your immune system more efficient.
Vitamin C taken in conjunction further potentiates the immune system.
There has been a lot of research into this substance, but not much
interest shown by the medical profession. Quite big in the cosmetics
industry though.

Works well in resolving skin cancer.
Some reading for you follows...

Regards - Ivan.


http://www.tldp.com/issue/184/Yeast%20Derived%20Beta.htm

Glucan anti-tumor effect can be local or systemic. A local injection
of beta-1,3-D-glucan suspension into melanoma lesions has been shown
to successfully resolve the tumor locally (Mansell, 1978). In these
human experiments, the site of injection revealed no previously
established tumor, but plenty of macrophages filled with pigments.
Obviously, macrophages were drawn to the site where they phagocytized
and destroyed pigment-bearing tumor cells. These intralesional
injections in some cases were able to control further growth of remote
metastasis of the same tumor which resumed growth after glucan
treatment withdrawal.

Unfortunately, no clinical applications were developed out of these
results until recently (Carrow, 1996). The latest data contains very
promising information, not only in regard to human melanoma, but also
to basal cell carcinoma.

http://www.arrowheadhealthworks.com/B13GRsh.htm


http://neuro-www.mgh.harvard.edu/forum_2/CongenFiberTypeDisproF/9.28.9
97.58PMMEDICALPROOF.html

-Original Message-
From: Marlene Hanson [mailto:mlehan...@msn.com]
Sent: Thursday, 4 April 2002 7:07 a.m.
To: *Silver-List* (E-mail)
Subject: Re: CSSilver Compounds and electrobiological/electromagnetic
response


Hi Ivan, What is 1, 3, Beta Glucans and would this work for skin
tumors?
Thank you Marlene

- Original Message -
From: I Anderson
Sent: Wednesday, April 03, 2002 4:27 AM
To: silver-list@eskimo.com
Subject: RE: CSSilver Compounds and electrobiological/electromagnetic
response

Jason,
just some comments on some of your message.

 When a tumor forms, it is very difficult to eliminate through
 dietary means
 alone, when the dietary changes do not directly address the
 tumor growth.
 The problem is a bioelectric one.  Dr. Becker demonstrated
 that a tumor, and
 cancerous cells in general, are the most positively charged of all
 tissues.

Bioelectrics, chemical potential, pH are all measures of the same
thing from different perspectives.
Cancer cells are the most positively charged of all cells because they
are the most acidic. Being acidic means a high concentration H+ ions
(high positive charge and low pH).
Cancer cells become highly acidic as a result of nutrients crossing
from a more acidic than normal extracellular fluid (plasma) which
causes a break down in the cellular channels which in turn does not
allow oxygen to pass into the cell. Without oxygen energy production
changes from oxidation to fermentation, the product of which is lactic
acid which accumulates and thus causes a large drop in pH.
Diet plays a great part in the pH of the extracellular fluid. Cancer
cells cannot grow in alkaline environments, because in these
environments oxygen is abundantly available and mutated cells either
lie dormant or die.
Calcium is the most important mineral in maintaining a healthy and
buffered serum pH, and ultimately the bioelectric condition of tissue.
Vitamin D is essential in the absorption of calcium. A diet which pays
attention to these facts, and is otherwise sensible, will be well
protective against cancer.

Large cancerous growths can be pretty readily eliminated through the
high pH method, skin cancers respond well to this also, or can be well
treated by the injection of 1,3 beta glucan into the base of the
cancer mass. I personally don't see the point of attempting electrical
treatment, but wish you luck, and look forward to discussing a
successful treatment.

Regards
Ivan.




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silver.

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RE: CScan anyone offer help

2002-04-04 Thread I Anderson
See my previous post Joanne.

Also take a look here:
http://www.polymvasurvivors.com/

Ivan.

-Original Message-
From: Joanne [mailto:sam...@snowcrest.net]
Sent: Thursday, 4 April 2002 5:30 p.m.
To: silver list
Subject: CScan anyone offer help


A friend sent me this letter he received from a friend and asked if
anyone over here might have any suggestions..
Thank you
Joanne


Hey... well, I found out today and its not great but
its not ... well, its not great...
its called synoval sarcoma.
It originates in bone so my fears of it spreading TO
bone was silly because it started there.  I'm going to
MD ANDERSON next thurs on the 10th and will go thru
some tests... I know they will test the rest of my
body (mri) to see if its spread and if not (WHICH I'M
REALLY REALLY REALLY HOPING NOT) then we will begin
with an operation.
I will have to have my radius removed as well as much
of my muscle.  I spoke with the surgeon about
rebuilding and he didn't look hopeful that it would be
a possibility because of all the nerve damage that
will occur. A numb limb is a useless one and dangerous
to have in many ways... so I will wake up to one of
two scenarios: the most likely is that my arm will be
removed just below or with the elbow, or (unlikely)
will have a skinny sickly scary looking tiny long thin
arm below the elbow that we'll reconstruct.  It all
depends on what they find inside so this all stinks!.
I'm angry but I'm becoming QUITE enlightened...  I'm
becoming crystal clear about a lot that would have
taken me many many years to understand. I wish I could
explain the changes in my perception and reality but
words fail.  Just know I'm getting a lot of positive
things out of this.
Sarcomas aren't killed off easily at all by chemo
which is why the removal thing is necessary with
them... high percentages of ppl who ever have a
sarcoma will get reoccurring ones.  But for now if it
hasn't spread and the cancer is removed from my arm I
will be cancer-free.
I'm lucky because its not my leg... or my pancreas or
something like that, if its just my arm...
I'm also lucky that it isn't my RIGHT arm.
I'm lucky to have people who care so much about me and
My town is lucky Im not a postal worker. hahahaha
just kidding.
Actually I'll just take everything one step at a
time... I figure if I'm going to the hosp on the 10th
I'll have tests, then the surgery very very soon
after, and chemo and, possibly, radiation.
woo hoo. fun. eek!
Thank you for keeping me in your thoughts.
I'm going to be ok. This is just hard.
heck. I did labor, right? :)
love,
Laura.


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RE: CSurinary track infection

2002-04-03 Thread I Anderson
Malcolm,

The pH of the blood plasma lies within the range of 7.3 to 7.5, this
is a critical range outside of which it is difficult to sustain life.
There is a system of buffers and defences which inhibit the extremes
in plasma pH. One of the most important is the mobilisation of calcium
from the bones to bond with (and thus neutralise) those acidic
compounds which would otherwise cause a drop in plasma pH.
Unfortunately, most calcium complexes are insoluble at these pH
levels, which are, after all slightly alkaline, and so precipitates
and stones form.

One way to overcome this problem in the short term is to supplement
with alkaline forming foods or supplements, which supply those more
caustic elements sodium and potassium. Sodium and potassium will
replace calcium in precipitates and render them soluble, so that they
might then be excreted by the kidneys.

In the long term, preventative measures which will ensure all round
good health, might include limiting phosphate consumption (red meat,
carbonated drinks etc.), vitamin D supplementation which ensures the
bioavailability of calcium supplementation, sunshine or at least full
spectrum light each day to ensure the hormone production for proper
calcium regulation.

Regards
Ivan.

 -Original Message-
 From: Malcolm Stebbins [mailto:s...@asis.com]
 Sent: Wednesday, 3 April 2002 9:03 a.m.
 To: silver-list@eskimo.com
 Subject: Re: CSurinary track infection


 Hi, I don't go along with your comment that an acidic
 environment in the urinary
 tract is linked to bladder or kidney stones, in fact I think
 it's just the
 opposite.  Generally the stones are a compound of calcium,
 and can even be
 dissolved by adding acidic solutions to a chunk of one.
 There may be something,
 or some form of stone, I don't know about, or maybe there is
 some bodily
 reaction to the constant presence of an acidic environment,
 so if you have
 knowledge about some specifics I'd like to learn of them.
 Quite often, bacteria hide inside the stones, thus avoiding
 total destruction by
 the usual antibiotic regimen, and after even months of pills
 they return when
 the ABX are gone and in a few days to a week or so, there you
 are, yucky pee
 again.
 Malcolm

 Kathie Jones wrote:

 I suppose, any variance from a standard range of normal
 is what the
  bacterium that are often the culprits for urinary tract
 infections are fond
  of. Other bacteria may well favor a more acidic environment
 that what is *
  normal * and decreasing acid levels would discourage their
staying.
Too much acid in *some* people, over a period of many
 weeks or months, is
  linked to kidney stones. BUT...often there is something
 else going on that
  is encouraging this * i.e. consumption of too much soda
 *high carbonic acid
  levels*, genetic predisposition, imbalances in other parts
 of the bodies
  digestive or endocrine system.
 All in all, it goes back to Vit C helps the body's
 immune system *kick
  in* and kick out bacterial invaders, and is known to be
 especially efficient
  at combating UTIs when combined with cranberry. I stopped
 using cranberry
  juice, and switched to tablets a long time ago as the sugar
 in the drinks
  actually did the urinary system a disservice when trying to
 fight and
  infection. I have had HUGE success when doing this for
 myself, my daughter,
  hubby and my dog. :-) Gotta keep all the family members happy! *G*
 
  Kathie
 
   Hm...
   I was always under the impression that bacteria, and viruses
   liked to live in an Acidic environment
  
   Grant..
  
   Kathie Jones wrote:
   
LOTS of vitamin C and CS will do amazing things! :-)
 And don't forget
cranberry tablets. The cranberry keeps the bacteria
 that is causing the
infection from being able to * adhere * to the urinary
 system walls, the
  C
makes the urine acidic * the bacteria like an alkaline
 environment*, and
  the
CS will kill the bacteria off.
   
Kathie
 
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RE: CSSilver Compounds and electrobiological/electromagnetic response

2002-04-03 Thread I Anderson
Jason,
just some comments on some of your message.

 When a tumor forms, it is very difficult to eliminate through
 dietary means
 alone, when the dietary changes do not directly address the
 tumor growth.
 The problem is a bioelectric one.  Dr. Becker demonstrated
 that a tumor, and
 cancerous cells in general, are the most positively charged of all
 tissues.

Bioelectrics, chemical potential, pH are all measures of the same
thing from different perspectives.
Cancer cells are the most positively charged of all cells because they
are the most acidic. Being acidic means a high concentration H+ ions
(high positive charge and low pH).
Cancer cells become highly acidic as a result of nutrients crossing
from a more acidic than normal extracellular fluid (plasma) which
causes a break down in the cellular channels which in turn does not
allow oxygen to pass into the cell. Without oxygen energy production
changes from oxidation to fermentation, the product of which is lactic
acid which accumulates and thus causes a large drop in pH.
Diet plays a great part in the pH of the extracellular fluid. Cancer
cells cannot grow in alkaline environments, because in these
environments oxygen is abundantly available and mutated cells either
lie dormant or die.
Calcium is the most important mineral in maintaining a healthy and
buffered serum pH, and ultimately the bioelectric condition of tissue.
Vitamin D is essential in the absorption of calcium. A diet which pays
attention to these facts, and is otherwise sensible, will be well
protective against cancer.

Large cancerous growths can be pretty readily eliminated through the
high pH method, skin cancers respond well to this also, or can be well
treated by the injection of 1,3 beta glucan into the base of the
cancer mass. I personally don't see the point of attempting electrical
treatment, but wish you luck, and look forward to discussing a
successful treatment.

Regards
Ivan.




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RE: CS100-500 PPM CS and how it's made.

2002-03-28 Thread I Anderson
Hi Marshall,

A few comments.
Firstly, whilst the concentration of chloride ions is high in the
stomach and may indeed combine with silver ions to form silver
chloride(solid), it drops to serum levels and below in the duodenum
where most metal absorption occurs. Some of any AgCl(s) will be
redissolved here in reflection of the lower Cl- concentration,
probably by a couple of orders of magnitude. If the chloride
concentration is higher than the Ag+ ion concentration then silver
chloride complexes such as AgCl2-(aq) will be formed as well as
AgCl(aq). Also other ions will compete for the chloride ion further
lowering its availability. And further more, other molecules will
compete for the silver ions' attention, these might include transport
proteins and enzymes, and vitamin D which acts as a facilitating
transport mechanism for metallic cations (M+).
Of the remaining silver chloride (solid), there is no reason to
believe that the size of the these molecules is too large to be
absorbed, indeed at least one study shows that silver chloride readily
passes through biological membranes.
Therefore it is entirely reasonable to believe that a large proportion
of ingested silver ions is available and absorbed.

Thus absorbed, the silver ions will bond to proteins and so on, but
much will still be available to replace the hydrogen in sulfhydryl
groups and disable pathogen function. Silver chloride will give up
silver to sulphide.

If the silver load is so large that it cannot be cleared by the bodies
chelating and disposal systems, and despite that to some extent no
doubt, some silver will bond to tissue, where it may be reduced to
silver metal by light and/or be reoxidised by light, depending upon
the composition of surrounding molecules.
And while to some degree the process of photography is similar, the
comparison is not really appropriate, due to the dilution of the CS
involved and the presence of a myriad of other molecules and
chemicals.
And lets be clear, particles of silver (as found in the CS you would
prefer to ingest) would be a ready building block for the development
of silver grains, such as you describe.

In saying all this, I am presuming that one is sensible about the
concentration and the amount of silver one ingests, it is entirely
possible to develop argyria by taking large amounts of silver (only
achievable by ingesting silver compounds) and being nutritionally
deficient in some areas and/or surficient in others.

I don't think any one is suggesting the ingestion 1000ppm silver
citrate complex.

Regards
Ivan

 -Original Message-
 From: Marshall Dudley [mailto:mdud...@execonn.com]
 Sent: Tuesday, 26 March 2002 3:31 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CS100-500 PPM CS and how it's made.


 Kevin Nolan wrote:

  Marshall; I seem to recall you making these same remarks a
 while back. I
  believe Ivan answered at that time that the response to light of
  concentrated silver acetate in a photographic emulsion can
 hardly be equated
  to what happens when a dilute solution is ingested in the
 human body.

 Yes, but I don't consider 500-1000 ppm as dilute.

 
  Following some negative comments by Bob Berger on the light
 sensitivity of
  CS brewed with citrate (actually, I think it was added
 potassium citrate,
  which is a very different situation), I tried an
 experiment. Left an old
  PETE jar containing ~ 20 PPM silver, brewed with excess
 citric acid, out in
  the sun over the entire summer period. The solution is
 still perfectly
  clear, with no signs of any dropout.

 But did you add the developer, and make the ph over 7?
 Without those two items,
 then development will not occur.  If it is still acid, then
 it cannot occur,
 in fact stop bath is normally acetic acid for that reason.

  I am not sure of the % ionic but there
  is a moderate to strong TE present. By the same token, many
 list members
  have reported light sensitivity of CS brewed with DW only -
 a sign their
  technique was wrong, rather than any inherent photosensitivity
with
  'traditionally brewed' CS.

 All photsensitivity does is cause a few of the silver atoms
 in a compound to
 reduce to silver atoms.  This is of virtually no consequence,
 the real problem
 is that more can reduce upon contact with the atom (or CS
 particle), and make it
 grow until it becomes stuck.  This does not require light,
 just the right
 chemistry, which blood is if you drink a cup of coffee.  THE
 REDUCTION OF A FEW
 IONS TO SILVER ATOMS IS OF NO CONSEQUENCE.  IT IS
 'DEVELOPMENT' THAT IS A
 PROBLEM.

  As far as silver citrate being 'another compound
  of silver' - so is predominantly ALL the CS made, whether
 HVAC or LVDC. The
  figures quoted are anywhere from 75-99 % ionic silver. Well
 it can't just be
  silver ions present - what you have is the COMPOUND silver
hydroxide
  (dissociated in solution as ions of course, just as silver
 acetate is). So
  the arguement is whether acetate ions are somehow more
 dangerous than
  

RE: CSRE: Thrush

2002-03-28 Thread I Anderson
Craig,

You might try beta glucan to control both the thrush and the candida.
Dissolve some in water and rinse the mouth... this can be used in
conjunction with other remedies.

ionic silver is more likely to be helpful than particulate... however
adding a few drops of H2O2 to particulate silver (colloidal) will make
it clear and ionic.

Regards
Ivan.

 -Original Message-
 From: Craig Chamberlin [mailto:c...@itsmyplace.com]
 Sent: Wednesday, 27 March 2002 9:04 p.m.
 To: silver-list@eskimo.com
 Subject: CSRE: Thrush


 Greetings list members,

 My sister has metastasized breast cancer.  The cancer isn't
 killing her
 but the inability to eat and drink because of the Thrush.  We can
get
 the candida which underlies the Thrush, if we can just get the
Thrush
 under control in her mouth so she can eat and drink.

 We have used high concentration CS (from Frank Rey, thank you
 for making
 this available), white oak bark and some allopathic swish 
swallow
 which didn't do anything...but neither did the others.

 We have been advised that 3% H2O2 is effective, won't know until
 tomorrow when she comes home.

 We are treating her for thrush with a 6C EM+ machine as well,
 but to no
 avail.  Mostly because she keeps getting dehydrated and it seems to
 deter the Rife Effect.

 I am wondering about a 5% Hydrochloric acid solution.

 I desparately need a thrush buster that works and works fast.  She
is
 small and has always been thin, so not much in reserve.

 Thanks for your help,

 Craig


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RE: CSsuspension

2002-03-28 Thread I Anderson
A single 9v battery makes pretty good CS, current runaway does not
seem to be a problem until you hit about 15ppm, just takes a lng
time. I would suspect the water if fallout continues after a couple of
days.

Ivan

 -Original Message-
 From: Ode Coyote [mailto:coy...@alltel.net]
 Sent: Friday, 29 March 2002 12:26 a.m.
 To: silver-list@eskimo.com
 Subject: Re: CSsuspension


 While I haven't experimented with a single nine volt battery, i
would
 suggest starting with the electrodes fairly close and
 spreading them apart
 every 10 or 15 minutes up to 2 or 3 inches at finish in order
 to keep the
 current draw low. If it turns significantly yellow..or any
 color at all,
 shorten the run time and reduce current.
  I presume you are using distilled water and no salt?
  My idea is, if it falls out, it's not colloidal silver. So, let
every
 batch settle and pour what's left off the top and use that. A
 laser pointer
 will tell you there's plenty of silver still suspended.

  Colloidal silver is not light sensitive, contrary to popular
 belief.  A
 clear plastic pop bottle or clear glass works just fine for storage.

  I suggest buying or making a current controlled generator.

 http://www.silverpuppy.com [basic and inexpensive, turns
 itself off, nice
 package] Ken

 http://www.silvergen.com [works well and has bells and whistles,
turns
 itself off and has variable controls] Trem

 http://www.wishgranted.com [don't know much about it but
 seems like it's
 OK] Vince

 Attached is a current control circuit that can be made for
 less than $5

 Ken

 
 So now of course I now make my own and because of friends
 have to make a
 lot. I use a small 9 volt battery powered generator. Mostly
 this is fine,
 however sometimes I have noticed that after 7,8 days the
 silver particles
 fall out of suspension and the fluid has to be shaken. Can
 anyone please
 help me on this matter? All my tools are glass except for
 some plastic
 spoons.  I store the output in brown glass bottles out of
 direct sunlight.
 Is 9volts enough, should I use a mains transformer? How far
 apart should the
 silver rods be spaced. What is the ideal water temperature.
 Any help will
 not go unnoticed.
 
 To conclude, I will be in New York  around the middle of
 April and would
 like to contact any subscribers in the NY area for a chat.
 
 DH


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RE: CSTahitain Noni

2002-03-28 Thread I Anderson
Hi Catherine,

You will find that a major active ingredient of Noni, barley, oats,
mushroom, Aloe, wheat grass, yeast and more, is the polysaccharide
1,3Beta Glucan.

There has been many studies done on this substance, but because of its
very high price (until recently) it is not widely known.

Ivan.

 -Original Message-
 From: Catherine Creel [mailto:ccr...@maine.rr.com]
 Sent: Thursday, 28 March 2002 2:42 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CSTahitain Noni


 Gladys it all depends on what you were taking the Noni
 Juice for.  One
 bottle will not tell you a thing

   we are a society that is promised magic pills by
 conventional medicine,
 and although nthey don't deliver, we have been indoctrinated
 into thinking
 this way so still look fro the magic pill in everything we try.

The benefits of Noni are well-documented. Below are two of
nineteen
 studies found at PubMed on Noni--Catherine


 Ann N Y Acad Sci 2001 Dec;952:161-8

  Cancer preventive effect of Morinda citrifolia (Noni).

 Wang MY, Su C.

 Department of Pathology, UIC College of Medicine, Rockford,
 Illinois 61107,
 USA. mianw...@uic.edu

 Morinda citrifolia (Noni) has been extensively used in folk
 medicine by
 Polynesians for over 2,000 years. It has been reported to have broad
 therapeutic effects, including anticancer activity, in both clinical
 practice and laboratory animal models. The mechanism for these
effects
 remains unknown. The hypothesis that Morinda citrifolia
 possesses a cancer
 preventive effect at the initiation stage of carcinogenesis
 was studied. Our
 preliminary data indicated that 10% Tahitian Noni Liquid
 Dietary Supplement
 or Tahitian Noni Juice (TNJ), made from Morinda citrifolia
 fruit by Morinda
 Inc, in drinking water for one week was able to prevent
 DMBA-DNA adduct
 formation. The levels of DMBA-DNA adducts were reduced by 30%
 in the heart,
 41% in the lung, 42% in the liver, and 80% in the kidney of
 female SD rats.
 Even more dramatic results were obtained in male C57 BL-6
 mice: 10% TNJ was
 able to reduce DMBA-DNA adduct formation by 60% in the heart,
 50% in the
 lung, 70% in the liver, and 90% in the kidney. In order to explore
the
 mechanism of this preventive effect, the antioxidant activity
 of TNJ was
 examined in vitro by lipid hydroperoxide (LPO) and
 tetrazolium nitroblue
 (TNB) assays. In the LPO assay, LPO oxidizes leucomethylene blue to
 methylene blue in the presence of hemoglobin. The resultant
 blue color was
 quantified at 660 nm spectrophotometrically. In the TNB
 assay, superoxide
 anion radicals (SAR) reduce TNB into formazan blue that was
 also measured by
 absorption at 602 nm. TNJ showed a dose-dependent inhibition
 of both LPO and
 SAR in our system. The antioxidant activity of TNJ was compared to
the
 effects of vitamin C, grape seed powder (GSP), and pycnogenol
 (PYC) at the
 daily dose per serving level recommended by U.S.RDAs or
 manufacturers. The
 results suggest that prevention of carcinogen-DNA adduct
 formation and the
 antioxidant activity of TNJ may contribute to the cancer
 preventive effect
 of Morinda citrifolia.

 PMID: 11795436
 

 Phytother Res 1999 Aug;13(5):380-7


 An immunomodulatory polysaccharide-rich substance from the
 fruit juice of
 Morinda citrifolia (noni) with antitumour activity.

 Hirazumi A, Furusawa E.

 Department of Pharmacology, John A., Burns School of
 Medicine, 1960 East
 West Road, University of Hawaii, Honolulu, HI 96822, USA.

 The fruit juice of Morinda citrifolia (noni) contains a
 polysaccharide-rich
 substance (noni-ppt) with antitumour activity in the Lewis lung
(LLC)
 peritoneal carcinomatosis model. Therapeutic administration
 of noni-ppt
 significantly enhanced the duration of survival of inbred
 syngeneic LLC
 tumour bearing mice. It did not exert significant cytotoxic
 effects in an
 adapted culture of LLC cells, LLC1, but could activate
 peritoneal exudate
 cells (PEC) to impart profound toxicity when co-cultured with
 the tumour
 cells. This suggested the possibility that noni-ppt may
 suppress tumour
 growth through activation of the host immune system.
 Concomitant treatment
 with the immunosuppressive agent, 2-chloroadenosine (C1-Ade)
 or cyclosporin
 (cys-A) diminished its activity, thereby substantiating an
 immunomodulatory
 mechanism. Noni-ppt was also capable of stimulating the
 release of several
 mediators from murine effector cells, including tumour
 necrosis factor-alpha
 (TNF-alpha), interleukin-1beta (IL-1beta), IL-10, IL-12 p70,
 interferon-gamma (IFN-gamma) and nitric oxide (NO), but had
 no effect on
 IL-2 and suppressed IL-4 release. Improved survival time and
curative
 effects occurred when noni-ppt was combined with sub-optimal
 doses of the
 standard chemotherapeutic agents, adriamycin (Adria),
 cisplatin (CDDP),
 5-fluorouracil (5-FU), and vincristine (VCR), suggesting
 important clinical
 applications of noni-ppt as a 

RE: CSTahitain Noni

2002-03-28 Thread I Anderson
Lucy,
If you re-read my message you will find that I noted that beta glucan
is a major active ingredient (perhaps I should have said constituent)
of all these foods. The positive health benefits that these foods
elicit will be due, at least in part, to the beta glucans.

In writing that message, I was inviting people to investigate the
properties of this rather amazing substance.

Ivan.


 -Original Message-
 From: Kimdane [mailto:kimd...@shaw.ca]
 Sent: Friday, 29 March 2002 3:18 a.m.
 To: *Silver-List* (E-mail)
 Subject: Re: CSTahitain Noni


 Ivan the ingredients of Morinda Tahitain Noni are:
 Reconstituted Morinda
 citrifolia fruit juice from pure juice puree from French
 Polynesia, natural
 grape juice concentrate, natural  blueberry juice
 concentrate, and flavours
 from all natural sources.
 Protein 0 gr Fat 0 gr Carbohydrates 3 gr Energy 10 cal
 None of the ingredients you listed are in Morinda Tahitian
 Noni. Morinda
 started producing noni juice.  Since then other companies
 have come on board
 but none have been able to be equal.

 Lucy Giesbrecht, Kimdane Reg
 Barf Fed Great Danes
 Tahitian Noni Juice
 An Exotic Health Discovery
 Winnipeg, Mb. Canada
 kimd...@shaw.ca
 ICQ 57495753

 - Original Message -
 From: I Anderson i...@win.co.nz

  Hi Catherine,
 
  You will find that a major active ingredient of Noni, barley,
oats,
  mushroom, Aloe, wheat grass, yeast and more, is the polysaccharide
  1,3Beta Glucan.



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RE: CS100-500 PPM CS and how it's made.

2002-03-25 Thread I Anderson
Still here Kevin, lurking in the background. Don't have much time
these days ...working on various projects. One is building a lab
beneath my new residence.

There is nothing on-line about this, I took my information from the
patent and my own investigations. I have not tried diluting a
concentrated solution, but see no reason for it not to be perfectly
stable. The only question that I have yet to answer, is just how
readily the silver becomes biologically available, but I should
imagine at concentrations below 285ppm the question is not relevant as
the ions are solvated and not complexed with the citrate (I presume).

Regards
Ivan.

 -Original Message-
 From: Kevin Nolan [mailto:ken...@optusnet.com.au]
 Sent: Monday, 25 March 2002 1:41 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CS100-500 PPM CS and how it's made.


 Hi Ivan,
 Was wondering whether you were still on the
 list. Are you
 aware of any on-line references on this matter? What happens
 when such a
 concentrate is diluted with water to various concentrations?
 Is the complex
 unstable at lower concentrations?

 regards, Kevin Nolan




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RE: CS250ppm fulvic acid ionic silver, good or not?

2002-03-25 Thread I Anderson
Dear Tang,

I see no problem with the ionic silver, but I am personally wary of
fulvic acid. Fulvic acid is a type of humic acid as found in various
soils, and as such its composition and action varies from place to
place. FA is a clathrate or chelate and a strong solvent, which may
penetrate all parts of the body. Some FA has been found to be
beneficial and some found to be implicated in various bone and liver
disease.
Please search the archives for 'fulvic acid' for some of the
information I have posted on this subject in the past, so that you
might be better informed.

Kind regards
Ivan.

 -Original Message-
 From: Huajun Tang [mailto:huajun_t...@yahoo.com]
 Sent: Monday, 25 March 2002 7:01 a.m.
 To: silver-list@eskimo.com
 Subject: CS250ppm fulvic acid ionic silver, good or not?


 Hello everyone,

 After reading the discusion on 100-500 PPM CS and how
 it's made, I begin to worry the 250ppm ionic silver
 made with fulvic acid that I am using to treat my
 candida problem. Is there any safty problem with this
 ionic silver?

 Any information will be highly appreciated.

 Thanks
 Huajun Tang



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RE: CSHi Ivan

2002-03-25 Thread I Anderson
Hi Arnold,
Nice to talk to you again!

Happy to repost, but not quite sure of the particular ones you had in
mind.
I have two (see below) which explain the rational behind current
limiting, and I shall try to find my calculations of the current
density.

Kind regards
Ivan.

Hi Arnold,

I think we need to start on common ground, so I will go through the
process as I understand it...you probably know all this anyway.

The power supply and the electrolysis cell form a circuit. The cell
consists of an electrolyte and 2 electrodes. Current is able to flow
in
the circuit when cations are able to leave one electrode and anions
contact the other. Electrons cannot flow in a liquid and so travel via
the power supply connections. In the case of a silver anode (positive
electrode), at a certain potential a single electrons will be removed
from silver atoms creating Ag+ silver ions. These cations, as they are
known, enter the liquid electrolyte and drift towards (and some will
eventually contact) the cathode where they are supplied with the
electron they need to become metallic silver once more.
The current able to flow in the circuit is wholly dependent upon the
conductivity of the electrolyte, that is the number of ions that are
able to complete the circuit.
Distilled water is a very poor electrolyte but above 0.71V hydrogen
will
reduce (gain electrons) at the cathode while silver requires 0.80V to
oxidise (lose electrons) at the anode. This is what drives the
reaction
at start up. Silver is oxidised at the anode, supplying electrons, and
hydrogen gas is generated at the cathode receiving electrons. The
limiting factor at this time is the number of hydrogen ions able to be
ripped from the water molecules, and this is a function of the current
flow and so of the applied potential.

As silver ions enter the solution and ultimately reach the cathode
they
are also reduced as the reduction potentials of hydrogen and silver
are
similar, and reducing hydrogen leaves a charged hydroxyl anions in
solution which adds to the accumulation of charged species, hence the
current increases. The reason that silver accumulates in the solution
at all, even though the same number of electrons oxidised at the anode
must be reduced at the cathode, is that the later is shared between
hydrogen and silver, that is more silver ions enter the system than
leave it.

What I am leading to Arnold, is that to achieve an acceptable
concentration of silver ions (10 -20 ppm in my opinion) one must
accept
a certain amount of plating out on the cathode, and that the process
is
not futile past this point as silver keeps accumulating as long as
hydrogen gas is evolved at the cathode.

Now, in order to generate a product that is of the smallest particle
size one must allow the silver ions to hydrate, to become surrounded
by
water molecules so that they resist the attractive forces that are
generated between like ions and limit the aggregation that otherwise
occurs. Limiting the current limits the amount of ions generated at
any
moment, increasing the chance of quick hydration and dispersion.
There is a certain current density at the electrode that when exceeded
leads to an inferior product.
The trouble with limiting the current of course is, as the resistance
of
the cell decreases so does the voltage. It is the voltage which
determines the type of electrolysis that will proceed (it is possible
to
remove more than one electron from a silver atom if the voltage is
high
enough). I feel that being able to control the voltage across the
electrodes will eventually lead to a better product. The only way I
can
think of to do this is by PWM which although, as you rightly note, is
a
method of controlling power input, it does so at a particular voltage
(yes?) and is also a method of limiting current. PWM would also have
the
advantage of the pulse - drift movement of the silver ions, further
increasing the chance of better hydration and dispersal.


and


In anticipation of your question, let me give a little more
information.

The velocity of an ion in an electric field is the product of the
field
strength
E(Vcm^-1) and its electrophoretic mobility U(cm^2 V^-1 s^-1).
The ion is instantly accelerated to the velocity where the resistive
forces (viscosity of medium etc.) equal the attractive forces, where
upon the ion travels at a constant rate.

v = EU(cm s^-1)

For silver ions (effective radius of 0.15nm) U = 6.4 x 10^-6.
Larger ions = slower speeds.
Higher charge = higher speeds.

So at a field strength of 1Vcm^-1 the velocity = 6.4 x 10^-6 cm s^-1
which is very slow unless you are an ion.

Obviously it is not the voltage that is the main diffusion factor in
CS
production but thermal or mechanically induced currents.


The link below (part of a marvellous body of work) gives a gentle
insight into the world of electrode dynamics, and the treatment of the
electrolyte solution as a resistive and capacitive load.


RE: CS100-500 PPM CS and how it's made.

2002-03-23 Thread I Anderson
Yes Marshall you are correct,
the solubility of silver citrate is 280ppm.
However it is thought that the silver-citrate complex formed by the
electrolysis of silver in a citric acid solution is either a
zwitterion where the negative charge is on the complex itself (Ag+CA-)
where the total charge of the complex is neutral, or the empty 5s
orbital of Ag+ overlaps with the delocalised .pi. bond on one of the
carboxyl groups of citric acid.

This concentration of silver is found when generated into a 10% citric
acid solution, higher citric acid concentrations allow higher silver
concentrations.

Ivan.

 -Original Message-
 From: Marshall Dudley [mailto:mdud...@execonn.com]
 Sent: Sunday, 24 March 2002 6:48 a.m.
 To: silver-list@eskimo.com
 Subject: Re: CS100-500 PPM CS and how it's made.


 That is interesting.  The solubility of silver citrate is 280
 ppm.  And of
 course the silver content of that would be less than the
 whole molecule.

 I wonder what the other part is doing.

 Marshall

 Kevin Nolan wrote:

  I recall Ivan Anderson stating he had managed to
 electrolytically produce ~
  1000 PPM CS (probably an ionic complex) via citric acid
 addition. Here is an
  excerpt:
  however it is known that brewing in a citric acid
 solution enables one
  to
  increase the silver content to more than a thousand ppm
 
  Kevin Nolan
 
  - Original Message -
  From: Russ Rosser russros...@rovin.net
  To: silver-list@eskimo.com
  Sent: Saturday, March 23, 2002 8:30 AM
  Subject: Re: CS100-500 PPM CS and how it's made.
 
   herbalhealer.com also has 500 ppm.  If it can't be made
 electrically
  without
   agglomeration, perhaps it's distilled down from a
 reasonablly concentrated
   batch??
  
   --Russ
  
  
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RE: CSOne last reversal experiment

2002-02-07 Thread I Anderson

Ivan - why the big difference(17.7 compared to 10-11)

Steve,
Could be that my multiplication factor is a bit high and the margin of
error of the conductivity meter (2% of full scale?), also you are
subtracting the starting conductivity reading from the end reading,
which is not something that I do (half of that reading will be due to
cations which will most likely plate out on the cathode).

If we look at the rise in conductivity:
straight run 0.8uS - 10.9uS a rise of 13.6 times.
switched run 0.8uS -  6.4uS a rise of  8.0 times.
vs. drop in resistance calculation:
straight run 220KOhms - 15K4Ohms a drop of 14.3 times
switched run 209KOhms - 27K7Ohms a drop of  7.6 times

we can see a good correlation between the two measurements (if it were
not so then something would be seriously wrong). Perhaps my 'silver
factor' should equal the conductivity meter adjustment factor.

Any way, good experiment, thanks a lot... this result is in line with
what I have predicted.

If you sill have the batches, could you do something for me? Could you
add a few drops of H2O2 (equal amount to an equal amount of each) and
see if one fizzes or becomes more cloudy than the other, This is a
simple test for the presence of metallic silver particles.

Regards
Ivan.



 -Original Message-
 From: S  J Young [mailto:you...@konnections.net]
 Sent: Thursday, 7 February 2002 6:00 p.m.
 To: Silver List
 Subject: CSOne last reversal experiment


 Hello again,

 Recently I reported results of comparing CS production of a
 control batch
 with constant current same polarity verses a batch produced
 with constant
 current but relay switched voltage reversals.  Brew time was
 4 hours with
 constant 30 RPM paddle stirring.  The result was the reversed
 batch was
 about 55% weaker than the control batch.

 Ole Bob did his best to convince me I did something wrong,
 and that the
 strength of the two batches should have been about the same.
 I thought
 perhaps I was trying to make too strong a brew, and I should
 cut down the
 brew time.  So I did another experiment as follows:

 Both cases were run for 3 hours with constant stirring at 55 degrees
F
 starting with 0.8 uS DW.  I use an electronically regulated
 constant current
 of about 1.11 ma.  I didn't have quite enough voltage to draw
 the full 1.11
 ma at the run starts, but the current was 1.11 ma for the
 majority of the 3
 hours.  Both brews look the same as the original DW-perfectly
 clear.   Here
 are the results.

 1) Control (no reversal):  Some gunk sluffed off the wires.

 Starting V=174.1  i=0.79 ma.  Starting Resistance=220KOhm
 Ending uS=10.9, V=17.4  i=1.13.  Ending resistance=15.4KOhm

 uS gain due to silver ions =10.9-0.8=10.1.  Using Ivan's 
 Frank Key's 
 Trem's conversion factor of 1 to 1.1, the PPM  is 10.1 to 11.1.

 Using Ivan's recently posted formula, PPM for ions =1.3 *
 Rstart/Rend =
 17.7.  Ivan - why the big difference (17.7 compared to 10-11)?

 2) Reversal:  Polarity switched each 60 seconds which Ole Bob
 says gives the
 best results.  Wires got black but no gunk sluffed off.

 Starting V=171.4  i=0.82 ma.  Starting R=209KOhm
 Ending uS=6.4, V=31  i=1.12.  Ending R=27.7KOhm

 PPM ala recent Ivan formula is 1.3 *209/27.7=9.8.

 uS gain due to silver ions=6.4-0.8=5.6.  So PPM ala Trem et
 al is 5.6-6.2.

 So this batch is 5.6 uS/10.1 uS * 100 = 55% weaker.

 So, sadly, I again conclude polarity switching produces
 significantly weaker
 ionic silver concentrations.  The first experiment showed that if
the
 reversed brew time is doubled, the strength was still not as
 much as the
 non-reversed case, and black pepper-like particles began to
 fall off the
 wires.

 Again, I conclude that I don't see any advantage to polarity
 switching which
 justifies the extra complexity.  I don't mind a bit of gunk
 sluff-off as I
 am able to decant off almost all the brew and leave the gunk
 behind in the
 jar.

 Someone else can continue with polarity reversal experiments
 - I think I
 have performed my last one.

 --Steve Young


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RE: CSLiving Water CS

2002-02-07 Thread I Anderson
Ah yes, this is what I thought also, until I realised that the ionised
hydrogen referred to is the H- hydride.

http://www.h-minus-ion.org/

any one take a guess at the method by which the magic jug works?
http://www.h-minus-ion.org/Methods-to-modify-ORP-water-1.html

Hmmmagreed!
Ivan.

 -Original Message-
 From: M. G. Devour [mailto:mdev...@eskimo.com]
 Sent: Thursday, 7 February 2002 11:59 a.m.
 To: silver-list@eskimo.com
 Subject: Re: CSLiving Water  CS


  Re: CSLiving Water  CS
 
  Hi:
 
  There are things that can be done to water that affects it's
surface
  tension and hydrogen ion concentration. For instance,
 bubbling ionized
  hydrogen gas through water, increases the pH and makes hydrogen
  available as the ultimate antioxident.

 I can understand H+ being an antioxidant, but wouldn't that
 *lower* the
 pH, ie. make it more acidic? Or is the Cl in HCl that makes
 an aqueous
 solution acidic? Damn. Chemistry class was a looong time ago.

 Hmmm... Interesting.

 Mike D.

 [Mike Devour, Citizen, Patriot, Libertarian]
 [mdev...@eskimo.com]
 [Speaking only for myself...   ]


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RE: CSLiving Water CS

2002-02-03 Thread I Anderson
One way to re-program water is to freeze it. This forces the molecules
to adopt a structured lattice. Thawing in sunshine is good. Magnets,
vortexes, ozone or what ever can then be applied.

BTW, if one skims the first formed ice, one can remove the deuterium
(D2O) component (for better or worse), as it freezes at a lower temp.

Ivan


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RE: CSBubbler System for CS and Commentary

2002-01-31 Thread I Anderson
Yes, you are right except in regards to stability.
Whilst the silver can't disappear, it can plate out on to the sides of
the container, or flocculate and settle out.
Being a manufacturer of CS, I probably have different expectations of
a quality CS than most users, to me stability is paramount as the
label must reflect the contents of the bottle even after sitting on
the shelf for a year or more. I also need to be prepared for some
authority testing the contents for purity.

However, I am the first to say that it is practically impossible to
make a CS that is not effective, no matter how simple the generator...
I am not one who believes that particle size is of great importance,
1nm or 50nm, it all seems to work... its just that the smaller the
particle size the more stable the colloid.

I should also note, that when I measure CS I measure the ionic content
primarily because that is what I endeavour to produce.

Glass bottles are intuitively the best container, but this is not
necessarily so. Positive ions (cations) will plate out onto glass, and
inert plastics are probably a better choice. Pure CS should not be
light sensitive.

Apart from electron microscopy, or 20nm syringe filters, there is no
cheap particle sizing.

Regards
Ivan.

-Original Message-
From: Marshall Jeffus [mailto:marshalljef...@yahoo.com]
Sent: Wednesday, 30 January 2002 7:12 a.m.
To: *Silver-List* (E-mail)
Subject: RE: CSBubbler System for CS and Commentary


Please consider the following discussion as coming from a limited
background, based on what little I know about CS:  the quality of CS
is not determined by ppm, but by particle size and purity.  Solution
ppm shouldn't typically change, even over long term, as the silver
can't just disappear.  However, it can clump into larger particles
(due to cohesive forces), rendering it ineffective.  It can also
combine molecularly with contaminants in the solvent (water) or the
container, which makes a good case for using inert (glass) bottles.
Also, keep in mind due to light degradation.  Particle size can be
tested, but not without cost.
Btw does anyone know of an inexpensive particle size tester?  I think
it's lab equipment, not a handheld like a TDS meter.
Would appreciate anyone who can either affirm or correct the above
information.
  I Anderson i...@win.co.nz wrote:
I guess it's a case of what ever works for you!
I have 10L of 3 year old CS, slight golden colour, that tests as
having the same concentration (22ppm) as the day it was made. And it
was made without any stirring at all, apart from the occasional hand
stirring during the 2.5 days it took to make it!

Regards
Ivan.



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RE: CSCS Fulvic Acid

2002-01-31 Thread I Anderson
Ric,

I can only direct you to the message I sent on the 25th which
contained some summaries and links to further info.
Some fulvic acid is implicated in liver cancer and bone problems, some
fulvic acids seem beneficial. Knowing which is which is not something
I am willing to trust to the market.

Regards
Ivan.

 -Original Message-
 From: Ric Stoll [mailto:r...@townsqr.com]
 Sent: Thursday, 31 January 2002 4:36 a.m.
 To: *Silver-List* (E-mail)
 Subject: RE: CSCS  Fulvic Acid


 Ivan, do you have a source for the following opinion?  I have been
 considering ingesting fulvic acid but sure wouldn't want to if it's
 detrimental.

 Thanks much.  Ric




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CSCS - HIV

2002-01-31 Thread I Anderson
CS does kill the HIV in the test tube.

There are individuals who have reported a drop in viral load as a
consequence of ingesting colloidal silver.

Here is a link to some good results:
http://www.health-truth.com/articles/hiv03.asp

There was some work done with electrodes inserted directly into the
arteries, with dramatic results, I suspect IV would produce similar
results.

There are many other approaches... interestingly virgin coconut oil
has or is being tested in the Philippines, about 4 tablespoons a day
seems to produce good results.

Ivan.

 -Original Message-
 From: Douglas De La Roca [mailto:ddelar...@nationalpeo.org]
 Sent: Thursday, 31 January 2002 4:41 a.m.
 To: silver-list@eskimo.com
 Subject: Re: CSChecking..JUst Ignore..


 Hello !
 I have a question and not sure who can help...but anybody giving any
 information will be of great help.  I been researching CS for
 a quiet a
 while now...
 My question is How effective is CS with HIV+
 if there a simple treatment or  prove that it even works?
 Please any comments on this email at stalin2...@aol.com
 Thanks so much for any help...
 i am 24 year old male...trying to understand this medecine.
 thanks
 DD


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RE: CSCS Fulvic Acid

2002-01-31 Thread I Anderson
Marlene,

No I don't think so are you thinking of malic acid?
Fulvic acid is one of the humic acids produced in the ground by the
decay of vegetable matter. It is a chelator, and is responsible for
the movement of toxic metal pollution from place to place.

Ivan.
  -Original Message-
  From: Marlene Hanson [mailto:mlehan...@msn.com]
  Sent: Thursday, 31 January 2002 6:35 a.m.
  To: silver-list@eskimo.com
  Subject: Re: CSCS  Fulvic Acid


  Hi Ivan, Isn't Fulvic Acid part of apple cider vinegar? I am
currently taking apple Vinegar for digestive and circulation problems.
Thank you Marlene



RE: CSCS Fulvic Acid

2002-01-30 Thread I Anderson
Yes Nancy, that is my opinion, and further, I would not personally
take any product that contained fulvic acid.

Ivan.

 -Original Message-
 From: Black [mailto:dbl...@cfl.rr.com]
 Sent: Saturday, 26 January 2002 9:35 a.m.
 To: *Silver-List* (E-mail)
 Subject: Re: CSCS  Fulvic Acid


 Thanks, Ivan.  so what you said is that Fulvic acid is both
 unnecessary and
 ill advised for use with CS?

 Nancy...



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RE: CScolloidal gold.

2002-01-30 Thread I Anderson
I think monoatomic gold has all of its electrons, they are just
arranged a little
differently ...hard to tell ;-)

Ivan.

 -Original Message-
 From: Russ Rosser [mailto:russros...@rovin.net]
 Sent: Saturday, 26 January 2002 8:12 p.m.
 To: *Silver-List* (E-mail)
 Subject: Re: CScolloidal gold.


  Russ,
 
  In this case it is the ionic form that is toxic. The ionic
 gold needs
  to be reduced to metallic gold before ingestion.

 ...Unless it's in monatomic form, of course!  :^)


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RE: CSbubbler solution?

2002-01-30 Thread I Anderson
A very good idea Willy

Thanks!

Ivan

 -Original Message-
 From: Satchid [mailto:satc...@sevaproductions.com]
 Sent: Tuesday, 29 January 2002 6:06 a.m.
 To: silver-list@eskimo.com
 Subject: CSbubbler solution?



 Hi,

 Would it not be good to when using a bubbler to pump it
 trough DW to purify
 the air, then into the CS maker?

 Here is how I would make it: Take a glass container +-1/2 liter with
a
 quick-lock lid. Then take 2 pieces of copper tubing 1/4
 diameter.   drill
 two holes in the lid and solder one tube in the hole so that it
almost
 reaches the bottom of the container; The second tube is
 soldered in the
 second hole so that it sits to about 1/4 from the top of the
 container.
 Fill the container with DW until 3/4 of the top. close the
 container and
 connect the lower pipe to your air supply. Then the upper
 tube is connected
 to the bubbler in the CS maker. If you now start pumping, then the
air
 bubbles and is washed in the first tank and then travels to the SC.

 Satchid,


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RE: CSCS and hospital use.

2002-01-29 Thread I Anderson
Annie,

The difference between CS and silver nitrate is the nitrate. Silver
ions as supplied by both CS and silver nitrate are benign, but the
nitrate is caustic to tissue. Highly diluted silver nitrate has been
used to good effect for many years in preventing nasty infections
passed from mother to baby during birth, but prolonged use of silver
compounds, especially silver nitrate, can be hazardous to health, if
not for the tissue damage, then by the large amounts of silver that
can be ingested or absorbed in the form of compounds (as opposed to
the very small amounts of silver delivered by colloidal silver).
Ingestion of large amounts of silver can lead to the cosmetically
disfiguring condition known as argyria, in which silver ions bound to
tissue, especially skin or eye, may be photo-reduced to silver metal
and cause a greying or bluing of the skin.

Regards
Ivan.

 -Original Message-
 From: Marshall Dudley [mailto:mdud...@execonn.com]
 Sent: Tuesday, 29 January 2002 4:44 a.m.
 To: silver-list@eskimo.com
 Subject: Re: CSCS and hospital use.


 Annie Hall wrote:

  Anyway, as an absolute newby can someone say what is
  the difference, in simple English, between silver
  nitrate and CS please?

 Big difference.  Silver Nitrate is a compound, and colloidal
 silver is the
 pure metal in very small custers.  An undeveloped film contains
silver
 compounds (such as silver nitrate or silver chloride), and
 the developed
 photograph contains very small silver particles, similar to a
colloid.

 Thus if silver nitrate is exposed to light, and a developer
 such as caffine,
 it will develop into silver particles which will appear
 black.  Not a good
 thing.

 Silver nitrate is also toxic, whereas silver metal and
 colloid is not.  Some
 theories as to how silver kills bacteria relay on it's catalytic
 propterites.  colloidal silver is a very good catalyst, but
 silver nitrate
 is a very poor catalyst.

 Marshall


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RE: CSNewbie

2002-01-29 Thread I Anderson
Dan,

Even the most modest generator will make acceptable colloidal silver,
be it clear yellow or golden. The primary difference will be in the
shelf life of the output. None of it will be harmful to ingest.

For a given concentration, clear CS will have the smallest particle
size, then yellow, gold through to grey. Aim for a light colour with a
strong beam (Tyndall Effect) as shown by a laser pointer shone through
the solution, until you are familiar with the process and its nuances.

Many people have been helped by CS made in a glass with two silver
electrodes draped over the side, connected to 1, 2 or 3 9V batteries.

Regards
Ivan.

-Original Message-
From: Dan Williamson [mailto:danw6...@mail.cannet.com]
Sent: Tuesday, 29 January 2002 7:29 a.m.
To: silver-list@eskimo.com
Subject: CSNewbie


I have only started looking at CS as a possible alternative to
conventional treatment for skin cancer. There seems to be so much
conflicting information on the net as to low voltage CS preparation
that I have hesitated making any. Are there any web sites out there
that give accurate information? Some sites say that the finished
product will be slightly yellow to golden in color the next day while
others say it will be clear. Could someone clarify this for me as I
intend to use the CS internally as well and I certainly don't need to
use something that is usless or harmful, this old body of mine is the
only one I have. Thanks   -dan


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RE: CSBubbler System for CS and Commentary

2002-01-29 Thread I Anderson
I guess it's a case of what ever works for you!
I have 10L of 3 year old CS, slight golden colour, that tests as
having the same concentration (22ppm) as the day it was made. And it
was made without any stirring at all, apart from the occasional hand
stirring during the 2.5 days it took to make it!

Regards
Ivan.

 -Original Message-
 From: Tel Tofflemire [mailto:telt...@home.com]
 Sent: Tuesday, 29 January 2002 4:47 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CSBubbler System for CS and Commentary


 Brooks I have been using the fish tank bubblier, and
 sometimes a Alpine
 Ozone Gen. for Cs, and I knew in my deepest of my being it
 was ok...I tested
 it by making with bubblier and with out, I could plainly see
 by my necked
 eyes that bubbled CS was better, it doesn't loose PPM setting
 on the shelf,
 and it stayed clear or maybe just a faint bit light purple
 color, but on
 first look appears perfectly clear..white background reveals a tint
of
 purple. ..Thank you Brooke for taking the time...\
 Tel Tofflemire
 Phoenix, AZ


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RE: CSCS Fulvic Acid

2002-01-25 Thread I Anderson

Some info on fulvic acid, which is a type of humic acid.

http://escribe.com/health/thesilverlist/m22663.html

http://escribe.com/health/thesilverlist/m26609.html

Ivan

 -Original Message-
 From: Black [mailto:dbl...@cfl.rr.com]
 Sent: Friday, 25 January 2002 4:43 a.m.
 To: silver-list@eskimo.com
 Subject: CSCS  Fulvic Acid



 While searching for some CS info for someone who wants to
 know exactly what
 CS is I came across a web site called Healix which claims
 that by adding
 Fulvic Acid to silver ions you get a better delivery of the CS to
the
 bloodstream.  Anyone heard of this?

 nancy...


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RE: CSfish aquarium air bubbler

2002-01-25 Thread I Anderson

Marshall,

You seem so sure that silver oxide exists in CS solutions ...why?

There is little, if any, molecular oxygen atoms in d. water, and none
produced at the anode, if silver is being ionised there as silver
ionises at 0.79V as opposed to the 1.6V (or there abouts) required to
rip oxygen from water molecules.

It is my understanding that the colour of CS solutions is a result of
the particle size.

The greyish build up on the cathode is simply reduced silver ions, ie
silver metal fluff.

Ivan.


-Original Message-
From: Marshall Jeffus [mailto:marshalljef...@yahoo.com]
Sent: Thursday, 24 January 2002 1:08 p.m.
To: silver-list@eskimo.com
Subject: Re: CSfish aquarium air bubbler


Thanks for the excellent suggestion.  Perhaps the bubbler whisks away
silver before it has a chance to burn.  If that's the case, it's the
movement of water that's important.  Burnt silver - that's silver
oxide, of course, which adds color to CS.  The darker the color, the
more of it, so I understand.  Also, what do you notice in the way of
oxide buildup on the electrode: the grayish solid stuff.  Less or
none?
What is your generator type?  LVDC or otherwise, what
voltage/amperage.  I'm new to all this and trying to find out what is
the best setup.
One other thing: what is your concentration (ppm).  My understanding
is that the clearer the liquid, the finer the particles.
Thanks for replying.  Like I said, I'm new to all this and am really
grateful for any input any of you may have out there on getting a
quality generator up and running.
Thanks,
Marshall
PS Melvin Wolf says that adding a very small drop of honey in
distilled water helps a lot.  Something about how it fixes the
electrical/magnetic properties of the water and allows for good
conduction without adding electrolyte.  Saw this on a web site.  What
do you know about this?
  Tel Tofflemire telt...@home.com wrote:
Marshall Jeffus ,
I use a small fish tank bubbler,  in a 2 qt glass jar. I get crystal
clear CS using the bubblier, and it stays clear. I put the bubblier in
the bottom of the jar, I use oxygen rated hose designed for breathing
bottled ox. with a stone defuser on bottom to slow the flow and make
tiny bubbles.  Some on the list said it was not the best way to do it,
so I tested for 2 days 48 hrs. using bubblier and not , my best CS was
using the bubbler...with out I got particles so large you could see
them , with bubblier, crystal clear.good luck...
Tel Tofflemire
Phoenix
Marshall Jeffus wrote:
 Please, more info on this aquarium air bubbler.  How is it used in
the process?  Do the air bubbles run over the silver electrodes?
  DJG ql...@tds.net wrote:
I have heard this affects the CS while making it. Any comments?



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RE: CScolloidal gold

2002-01-25 Thread I Anderson
Willy,

Is the conductivity of your solution increasing?

Ivan

 -Original Message-
 From: Satchid [mailto:satc...@sevaproductions.com]
 Sent: Saturday, 26 January 2002 12:04 a.m.
 To: *Silver-List* (E-mail)
 Subject: CScolloidal gold



 Dear listers,

 Is it necessary to have a colored CG to have a working
 solution? Is it not
 as with CS that if more color (yellow for silver) that there is more
 particles clustered together. I find that when making CG that there
is
 already a good strong TE before the color is visible.

 Thank

 willy


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RE: CSfish aquarium air bubbler

2002-01-25 Thread I Anderson
Marshall D,

Thanks for your reply, and thanks for the informative link g

Try this, for an insight to the process of electrolysis, just
substitute Ag (0.79V) for chlorine at the anode.
http://scifun.chem.wisc.edu/chemweek/cl2naoh/Cl2NaOH.html

Silver hydroxide can only degrade if it is a compound and not
dissolved ions Ag+ and OH- . If water is being reduced to H2 gas at
the cathode (0.83V) then most likely silver is not (0.79V). H2 gas is
formed at the start of the process when no silver ion are available
for  reduction, and intermittently throughout the generating process
when Ag+ concentration is low in the cathode vicinity, or so I
theorise.

Regards
Ivan.


 -Original Message-
 From: Marshall Dudley [mailto:mdud...@execonn.com]
 Sent: Saturday, 26 January 2002 4:58 a.m.
 To: *Silver-List* (E-mail)
 Subject: Re: CSfish aquarium air bubbler


 I Anderson wrote:

  Marshall,
 
  You seem so sure that silver oxide exists in CS solutions ...why?
 
  There is little, if any, molecular oxygen atoms in d.
 water, and none
  produced at the anode,

 Hun?  Electrolysis produces oxygen at the anode.
 http://webhome.idirect.com/~famistew/hydrogen/electro.htm

  if silver is being ionised there as silver
  ionises at 0.79V as opposed to the 1.6V (or there abouts)
 required to
  rip oxygen from water molecules.
 

 In the later stages of production, if the current is allowed
 to go way up, I
 have seen bubbles produced at both electrodes.  If hydrogen is being
 produced at the cathode, then 1/2 as much oxygen HAS to be
 produced at the
 anode. You can't produce one without the other beyond the
 absorption level
 of water.

 
  It is my understanding that the colour of CS solutions is a
 result of
  the particle size.
 

 Absolutely.

 
  The greyish build up on the cathode is simply reduced
 silver ions, ie
  silver metal fluff.

 I think there is silver oxide when the process is run too
 long.  First when
 that happens the CS will get a bitter taste which I associate
 with being
 alkaline.  With silver, hydrogen and oxygen as the only
 elements present,
 silver oxide and silver hydroxide are the only compounds I
 know of that can
 do this.  Theoretically silver hydroxide could be made at the
 cathode, and
 silver oxide at the anode, where there is lots of free
 monoatomic hydrogen
 or oxygen.  Silver hydroxide spontaneously degrades to silver
 oxide rather
 quickly, so I believe that there can be trace amounts of it
 present in CS
 that is overdone, and that is what contributes the bitter taste.

 Marshall


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RE: CScolloidal gold.

2002-01-23 Thread I Anderson
Russ,

In this case it is the ionic form that is toxic. The ionic gold needs
to be reduced to metallic gold before ingestion.

Has any one thought of LVDC or LVAC arcing under water ...why does it
need to be HV?

Ivan

 -Original Message-
 From: Russ Rosser [mailto:russros...@rovin.net]
 Sent: Wednesday, 23 January 2002 4:30 a.m.
 To: silver-list@eskimo.com
 Subject: Re: CScolloidal gold.


 Yes, salts can be toxic; however, a theory I've had about other
ionic
 compounds may apply here:  If gold chloride naturally
 dissolves into an
 ionic solution in water, then the chloride might be separated
 out by means
 of a water ionizer.

 In 2000, the CS list had a thread about dietary minerals
 wherein Duncan
 initiated a sereis of posts titled, It's the ionic form that
 really works.
 Simultaneously, a discussion was underway regarding a good calcium
 supplement.  While various (expensive) brands were mentioned,
 I got the idea
 of buying CHEAP (50 lb. bags of) calcium  magnesium
 chloride, dissolving
 them in water and running that through a polarizer to achieve
 an aqueous
 solution of pure Ca+ and Mg+ (and OH-).

 Now those machines can be outrageously expensive, so I began
 musing over how
 I might build one.  The platinum coated electrodes, which
 catalytically
 protect the (usually titanium) substrate against acidic
 corrosion, are the
 prime expense, so I was investigating alternatives (carbon
 rods, iridium
 compounds, conductive polymers) when more mundane concerns took
 precedence...but it still might be worth pursuing and pertinent to
CG.
 Thoughts?

 --Russ

 - Original Message -
 From: Marshall Dudley mdud...@execonn.com
 To: silver-list@eskimo.com
 Sent: Monday, January 21, 2002 9:21 AM
 Subject: Re: CScolloidal gold.


  I want to warn everyone that gold salts are reported to be
 quite toxic I
  believe.  So be careful that you have NO salts left.
 
  (I have not verified this information, it came from a
 doctor discussing
 gold
  shots for people who have arthritis)
 
  Marshall
 
  Kevin Nolan wrote:
 
   Thanks again Ivan. Any thoughts on the best reagents to
 precipitate gold
 as
   colloid, concentrations to use etc? Looks like we're homing in
on
 something
   here - possibly that thing at the end of the rainbow!
  
   regards, Kevin Nolan
  
   - Original Message -
   From: I Anderson i...@win.co.nz
   To: silver-list@eskimo.com
   Sent: Monday, January 21, 2002 8:06 PM
   Subject: RE: CScolloidal gold.
  
Kevin,
   
Yes quite cost effective. 1g of gold chloride will make
 49L of 10ppm
colloidal gold.
   
In Australia you can obtain supplies here:
   
http://www.proscitech.com.au/
   
ProSciTech
PO Box 111
Thuringowa Qld 4817
Australia
   
Street Address:
37 Framara Dr, Kelso, 4815
   
C106 Gold Chloride AU$58.00 1g 10% discount for 10 x 1g
   
GOLD CHLORIDE hydrate
H(AuCl4) :H2O. F.W. 229.79
Chloroauric acid; hydrogen tetrachloroaurate; gold
 trichloride, acid.
Assay 99.9985%. Gold content 49%+.
Used in histology for staining of nerves. This highly
 purified gold
compound may be used for the preparation of colloidal gold
sols.
Golden-yellow to reddish, highly hygroscopic, crystals.
 Deteriorates
readily in UV light, is caustic on skin, dissolves well
 in water and
alcohol. M.S.D.S
C106 Gold Chloride, 1g (ampoule) Price
   
 -Original Message-
 From: Kevin Nolan [mailto:ken...@optusnet.com.au]
 Sent: Monday, 21 January 2002 2:50 a.m.
 To: silver-list@eskimo.com
 Subject: Re: CScolloidal gold.


 Thanks, Ivan. So where does one purchase gold chloride, and
 is it economic
 compared with electrolytically making from gold wire
 or similar?

 regards, Kevin Nolan

 - Original Message -
 From: I Anderson i...@win.co.nz
 To: silver-list@eskimo.com
 Sent: Sunday, January 20, 2002 11:28 AM
 Subject: RE: CScolloidal gold.


  Yes Kevin,
 
  But then why go to the trouble of electrically
 generating ionic
gold
  when one can purchase soluble gold chloride.
 
  Chemical reduction of gold chloride by various compounds
 (tannic acid,
  sodium citrate, etc.) as you mention is the traditional
way
 of making
  commercial and batch quantities of CG, as used in large
 amounts by the
  bio-chemistry industry. With the ability to
 regulate a uniform
  particle size from about 6nm +, it would seem to be
 the way to go.
 
  Regards
  Ivan.
   
   
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colloidal
 silver.
   
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 http

RE: CScolloidal gold.

2002-01-23 Thread I Anderson


 -Original Message-
 From: Kevin Nolan [mailto:ken...@optusnet.com.au]
 Sent: Tuesday, 22 January 2002 5:03 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CScolloidal gold.


 A valid point. This article:
 http://www.belmarpharmacy.com/library/reference2a.html
 from a site suggested by Ivan contains references to some
 toxic effects of
 various gold salts. Pure CG is given a clean bill of health
 re toxicity.
 Might pay to steer clear of chemical methods unless accurate
 determination
 of residual salts can be made.

 Kevin Nolan

If one uses sodium citrate, then as long as more than enough is added
to reduce the gold, the only ions that could remain in solution are
citrate, sodium, or chloride, all of which are perfectly harmless.

Ivan.


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CSColloidal gold - chemical method

2002-01-22 Thread I Anderson

paper on best practice.
http://www.devicelink.com/ivdt/archive/01/03/001.html

Let alfalfa reduce gold(III) salts to colloid particles for you.
http://www.engg.ksu.edu/HSRC/98Proceed/11Gardea2/11gardea2.pdf


Ivan.


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RE: CScolloidal gold.

2002-01-21 Thread I Anderson
Kevin,

Yes quite cost effective. 1g of gold chloride will make 49L of 10ppm
colloidal gold.

In Australia you can obtain supplies here:

http://www.proscitech.com.au/

ProSciTech
PO Box 111
Thuringowa Qld 4817
Australia

Street Address:
37 Framara Dr, Kelso, 4815

C106 Gold Chloride AU$58.00 1g 10% discount for 10 x 1g

GOLD CHLORIDE hydrate
H(AuCl4) :H2O. F.W. 229.79
Chloroauric acid; hydrogen tetrachloroaurate; gold trichloride, acid.
Assay 99.9985%. Gold content 49%+.
Used in histology for staining of nerves. This highly purified gold
compound may be used for the preparation of colloidal gold sols.
Golden-yellow to reddish, highly hygroscopic, crystals. Deteriorates
readily in UV light, is caustic on skin, dissolves well in water and
alcohol. M.S.D.S
C106 Gold Chloride, 1g (ampoule) Price

 -Original Message-
 From: Kevin Nolan [mailto:ken...@optusnet.com.au]
 Sent: Monday, 21 January 2002 2:50 a.m.
 To: silver-list@eskimo.com
 Subject: Re: CScolloidal gold.


 Thanks, Ivan. So where does one purchase gold chloride, and
 is it economic
 compared with electrolytically making from gold wire or similar?

 regards, Kevin Nolan

 - Original Message -
 From: I Anderson i...@win.co.nz
 To: silver-list@eskimo.com
 Sent: Sunday, January 20, 2002 11:28 AM
 Subject: RE: CScolloidal gold.


  Yes Kevin,
 
  But then why go to the trouble of electrically generating ionic
gold
  when one can purchase soluble gold chloride.
 
  Chemical reduction of gold chloride by various compounds
 (tannic acid,
  sodium citrate, etc.) as you mention is the traditional way
 of making
  commercial and batch quantities of CG, as used in large
 amounts by the
  bio-chemistry industry. With the ability to regulate a uniform
  particle size from about 6nm +, it would seem to be the way to go.
 
  Regards
  Ivan.


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RE: CSPolarity Switch Experiment

2002-01-21 Thread I Anderson
Hi Kevin,

You may be right, most of the current sag may well be in the build up
of charge in the electrode/water double layer. And without in depth
study I am not in a position to argue the toss. But it undoubtedly
true that the current passes through zero at each polarity change
...how much this slows the reaction I cannot say.

Here is a nice site with some info ...also on various rotating
electrodes.

http://www.bath.ac.uk/~chsacf/java/electrochemistry/elec/l6html/cvac.h
tm


Regards
Ivan.

 -Original Message-
 From: Kevin Nolan [mailto:ken...@optusnet.com.au]
 Sent: Monday, 21 January 2002 2:42 a.m.
 To: silver-list@eskimo.com
 Subject: Re: CSPolarity Switch Experiment


 Ivan - inertial effects are completely negligible in any
 electrolysis setup.
 The relaxation time (roughly a dividing line between
 resistive and inertial
 response) for ions in water is I think of the order of 10^-13
 seconds or so.
 Even taking the electrolysis setup - container plus DW plus
 electrodes, as a
 capacitor, the electrical system relaxation time would be
 much less than a
 microsecond. The rise and fall in current is undoubtedly a
 consequence of
 the electrodeposition and subsequent dispersal of a
 semi-insulating deposit
 on the electrodes - the 'plate-out' of silver. Current fluctuation
is
 mirroring electrode surface resistance fluctuation.

 regards, Kevin Nolan


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RE: CSPolarity Switch Experiment

2002-01-21 Thread I Anderson
Sound like a nice unit.
Thanks Trem.

Ivan.

 -Original Message-
 From: Trem [mailto:t...@silvergen.com]
 Sent: Monday, 21 January 2002 7:27 a.m.
 To: *Silver-List* (E-mail)
 Subject: RE: CSPolarity Switch Experiment


 Hi Ivan,

 I don't have any reference point because we never did run the units
 un-switched.  The electrodes are only 3/8 or so apart and
 are corrugated
 for rigidity. I needed a way to either clean them manually or
 have them be
 self cleaning.  I didn't think users would be very handy at
 cleaning them
 without damaging them, so, reversing current was my only
 option.   I used
 close spacing to have a high gradient in the water which
 would force the
 process to start quickly using startup voltages around 70
 volts.  Everything was a tradeoff.

 We are running about twice the current density on the
 switching unit as
 compared to the un-switched one but they both seem to make
 the same ratio
 of ionic to particulate silver.  Am using about 15 times the
 surface area
 of silver on the switched unit compared to the un-switched
 one.  Beats me
 why they have the same ratio..maybe when one is using
 very low current
 density it just works out that way.  With 4 electrodes 1.5 X
 5 wetted
 depth connected in parallel sets so that cathodes and anodes
 are always
 sandwiched between 2 electrodes (except for 1 end electrode)
 we run 30
 ma.  I'm having a tough time explaining electrode
 configuration here...hope
 you understand my meaning.

 Your explanation of the sag we experience after each reversal
 sounds good
 to me.  With good water flow between electrodes it is minimized
 however.  We use a submergible pump to keep it all in motion
 so there isn't
 an area of stagnant ions between electrodes that has to be turned
 around.  They are all in continuous motion.

 Trem


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RE: CSdog bites

2002-01-21 Thread I Anderson
Sounds like you've got it covered Jim.
Perhaps infra-red heat lamp or LED's or laser pointer will help to
heal faster.

Best wishes
Ivan.
  -Original Message-
  From: Acmeair [mailto:res00...@gte.net]
  Sent: Monday, 21 January 2002 10:45 a.m.
  To: silver-list@eskimo.com
  Subject: CSdog bites


  my ex- is a volunteer at the local animal shelter, in a group that
tries to adopt out the inmates. she was working with a mal-treated 12
year old, that was scared to death. it spooked on her, and bit her
real bad in the face. stitches in the lip, and a lot of teeth marks
just under the eye.

  the doc sewed her up and prescribed the standard anti-biotics. by
the time i heard about it, fever had set in , along with all the
swelling. she insisted on taking the anti-biotics, but did agree to
drink  CS, and keep a CS dampened cloth with the ice pack she is to
use. i've got her to keep cleansing the wounds with a cotton ball
soaked with CS, and to dring a cup of  CS 4 times a day.. i think i'll
tell her to cleanse the wounds with h2O2, also.

  any other things i could prompt her on???TIA jim, O+, S


RE: CScolloidal gold.

2002-01-21 Thread I Anderson
Well Satchid,

If you look at this study, you will find that it used at much higher
doses that can be supplied by HVAC method (for serious cases).

http://www.belmarpharmacy.com/library/reference2a.html

Regards
Ivan.

 -Original Message-
 From: Satchid [mailto:satc...@sevaproductions.com]
 Sent: Monday, 21 January 2002 10:38 p.m.
 To: *Silver-List* (E-mail)
 Subject: RE: CScolloidal gold.


 Ivan,
 Is this CG the usable in the same way as the CG made with the
 HVAC device?

 Satchid



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RE: CSquestions: stir vs. bubble

2002-01-19 Thread I Anderson
Gaston,

I tried bubbling with first with air and then argon. I found in using
air that I was seeing a definite Tyndall Beam (TE for Alison) with
many sparkles, which is not acceptable in my product. Argon was
better, but too expensive, so I only use that as a pressure source for
my filter (0.2um so that I can claim filter sterilisation). I find a
slow mechanical or thermal stirring to result in a perfectly clear
product with no TE. The selection of a very small current density is
the secret of fine CS, and my small commercial generators use this to
good effect, generating 15ppm in 500mls in about 2.5 hrs with no
stirring required (however I do recommend stirring by hand two or
three times during the run).

But to be honest, I have not compared the actual silver concentration
vs. conductivity of bubbled and stirred CS, which is why I only
suggested an increase in conductivity due to CO2 inclusion, which
never the less I believe to highly likely.

Regards
Ivan.

 -Original Message-
 From: Gaston [mailto:obouc...@colba.net]
 Sent: Saturday, 19 January 2002 2:33 a.m.
 To: *Silver-List* (E-mail)
 Subject: Re: CSquestions: stir vs. bubble


 Hi Ole Bob

 I see the reply from Ivan about CS that will probably read
 higher when using a bubbler instead a stirrer.

 Have you had a chance of comparing the two to prove that pls ?

 I presume that Ivan has done so.

 Gaston

 =
 - Original Message -
 From: I Anderson i...@win.co.nz
 To: silver-list@eskimo.com
 Sent: Friday, January 18, 2002 3:46 AM
 Subject: RE: CSquestions: stir vs. bubble


  Connie,
 
  A couple of thoughts come to mind:
 
  The stirrer does not mix too well.
  You are trying for too high a concentration.
  The bubbler introduces CO2 gas to the water, which will ionise and
  give a false (high) reading.
 
  If you are finding a change in the CS when exposed to light
 then it is
  possibly due to the quality of your water.
 
  Regards
  Ivan.


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RE: CScolloidal gold.

2002-01-19 Thread I Anderson
Satchid,

The standard reduction potential of gold is
1.52V Au --- Au+++ or 1.83V --- Au+.
The only thing that stops this reaction occurring at near this voltage
is electrode polarisation, which may be overcome in an acidic
solution.
Note that this method results in ionic gold and perhaps should not be
taken.

Regards
Ivan

 -Original Message-
 From: Satchid [mailto:satc...@sevaproductions.com]
 Sent: Saturday, 19 January 2002 7:26 a.m.
 To: silver-list@eskimo.com
 Subject: CScolloidal gold.



 I tried today (probably still with the right transformers to
 make colloidal
 gold. I could not get good result. the one transformer is to
 low voltage
 (4500 V 100 ma) the other is 8000V 50 Ma.
 I decided to try the low voltage way again but not that low.
 So, I took a
 Diode bridge and connected the AC side directly to the main
 240v then I
 connected the positive to the gold electrode the negative to a
silver
 electrode. At first I had current but it stayed almost stable. Then
It
 started slowly to go up from 1.35 ma and it is now already at
 9 ma and this
 after about 45 minutes. For this I used no current limiting.
 Do you think that I have colloidal Gold?

 Thank You

 Satchid


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RE: CSQuestion about saline other stuff

2002-01-19 Thread I Anderson
Hi Laura,

 -Original Message-
 From: gotoh...@aol.com [mailto:gotoh...@aol.com]
 Sent: Saturday, 19 January 2002 3:54 p.m.
 To: silver-list@eskimo.com
 Subject: CSQuestion about saline  other stuff


 Sorry to be so ignorant, I am definitely not good at
 chemistry, but my
 question re: saline and the concern about sodium chloride, it
 is only if used
 when making the cs, or does it also apply when mixing
 together such as in a
 nasal spray?

Some people put saline in their nasal spray, I don't myself.

Also, my first quart batch of cs I stored in
 amber bottles, the
 color was almost clear. The second batch I put in one of the
 distilled water
 bottles which was opaque, and the color was clearish until
 the next day when
 I had it in my truck for a couple of hours and it got kind of
 warm, but not
 hot. It changed to a grey color. Was that because of the
 container being too
 light, or the warmer temp. or a combination of both, and
 would it still be
 okay to use or should it be discarded?

Could be out gassing from the container affecting the stability of the
CS. There is no reason to expect clear CS with light TE to be affected
by light or heat. I would not use it myself.

Third batch, I put
 some in a clear
 glass, and added a little bit of salt for the chloride test,
 and the cs
 stayed almost the same, just a tiny bit cloudy. What does
 that indicate?

That you have a percentage of silver ions in your CS, it is behaving
as expected.

Next
 question, I am planning to purchase a ppm tester, do the less
 expensive ones
 work okay? (the 25.00 price range). Please forgive my
 ignorance, I want to
 use cs for life, and want to do it right!

You need a conductivity meter which measures in the 00.0 - 99.9 uS
(microseimen) range. A Hanna PWT (pure water tester) or equivalent.


 Laura H.
Regards
Ivan


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RE: CSPolarity Switch Experiment

2002-01-19 Thread I Anderson
Nice test Steve, thanks.

 What is interesting is that at polarity
 reversal time, the
 voltage rises up and settles back to the pre-switch voltage
 in just a few
 seconds.  Thus one would think the production strength would
 not be affected
 more than 10% or so instead of over 50%.

Well it is not the voltage that indicates the rate of silver
dissolution. The current dip and restoration will be more indicative,
and as Kevin mentioned, some of the energy will used in undoing what
was done in the last cycle, and as he mentioned later, it is likely
that a higher proportion of metallic colloid particles are produced. A
test of total silver content for both runs would be very interesting.

Ivan

 -Original Message-
 From: S  J Young [mailto:you...@konnections.net]
 Sent: Saturday, 19 January 2002 4:38 p.m.
 To: Silver List
 Subject: CSPolarity Switch Experiment


 List,

 I performed the following experiment:

 Case 1 was to make one quart of CS using a constant 1 ma DC
 current for 4
 hours with electrodes spaced about 2 inches and with constant
 stirring.
 Starting V= 173.7 volts, I=0.86 ma, so R = 202K.  Ending V =
 13.8, I=1.18
 ma, so R= 11.7K.  Using Ivan's formala, the PPM was
 1.3*(202/11.7) = 22.4
 PPM.   uS measured 14.5 with Hanna PWT.  At the end there was
 some gunk
 which sluffed off the wires and sunk to the bottom.

 Case 2 is exactly the same as Case 1, except the polarity was
 reversed about
 every 45 seconds.  Start V=168, I=0.96 so R=175K.  End V=30, I=1.16
so
 R=25.9K.  PPM calculates to 8.8 and measured 6.7 uS.  Both
 wires were black,
 but no gunk was produced.

 Both batches have very faint Tyndall effect, visiable only in
 a dark room.
 Case 1 was slightly more visible.  Both were made with
 Wallmart DW which
 measures around 1 uS with the PWT.

 So it is obvious to me that polarity reversing definitely
 produces a weaker
 batch.  Case 1 is (14.5-1)/(6.7-1) = about 2.4 times
 stronger, comparing uS
 measurements.  Or, case 1 is 22.4/8.8= about 2.5 times higher
 PPM using
 Ivan's formula.

 Granted this was not a highly controlled experiment.  One
 quart jar may have
 had a bit more residual silver which had plated out on the
 glass than
 another.  I may not have filled the jars to exactly the same
 level, the 120
 volt line voltage may have been a bit different, etc.  But
 the difference
 (more than a factor of 2) between polarity reversal and not
 is much too
 large to be explained away be sloppy experiment procedures.

 So it appears that one must run their constant current
 generator a bit more
 than twice as long if polarity reversal is used to end up
 with the same PPM
 for no reversal.  What is interesting is that at polarity
 reversal time, the
 voltage rises up and settles back to the pre-switch voltage
 in just a few
 seconds.  Thus one would think the production strength would
 not be affected
 more than 10% or so instead of over 50%.

 So, fellow scientists, why the big drop in uS or PPM when
 polarity switching
 is used?  How about if some of you repeat the experiment to ensure
my
 findings are valid?  I suspect similar results will occur even if
your
 generator is not constant current (e.g. 3 9 volt batteries).

 --Steve


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RE: CSfirst batch

2002-01-19 Thread I Anderson
Hi Alison, congratulations on your first batch!

It is not always possible to see any reaction at all from the
electrodes, depending upon the generator set-up. But the taste test
should prove whether you have succeeded or not (most unlikely not to
succeed). Also you should notice that one electrode darkens and the
other goes grey, and may have a film build up.

A laser pointer shone through the solution will show a light beam (TE
or Tyndall effect), which is another good indicator, although in some
cases this will be very faint, even in a dark room.

CS will be stable indefinitely or for only a couple of weeks,
depending upon how it was made. When you find black fall-out on the
bottom of your storage container it is probably on the way out.

Regards
Ivan.

 -Original Message-
 From: aliso...@ihug.co.nz [mailto:aliso...@ihug.co.nz]
 Sent: Saturday, 19 January 2002 7:17 p.m.
 To: silver-list@eskimo.com
 Subject: CSfirst batch


 My mother and I made our first batches of CS today. ( I had made
 a trial batch using boiled water last week but only got my distilled
 water yesterday - and Mum had to wait till yesterday for me to get
 the generator that I made for her to her)

 I was very happy with mine - after about 15 mins one rod had
 bubbles rising from it and the other had the finest wisps coming off
 it so I timed it 5 mins from then.  I plan on drinking 40mls a day,
 more if I feel myself coming down with something.

 My mothers batch, even after an hour she could not see wisps
 tho she had the rising bubbles and the tarnished rods.  Can we
 assume that she has made CS?  Yes, she did use distilled water
 at room temperature.  She is 65 and her eyes are not as good as
 they once were.  Maybe there is a possibility that she just didnt
 see the wisps as they were so fine.  I would be grateful for any
 opinion here.  What indication does one get when the batteries are
 going flat?

 Also, what is the shelf life of CS?  I was wondering about putting
 some in a small bottle and keeping it in my handbag for any
 eventuality.  Does anyone else do this?  Is it adviseable?

 Alison
 in New Zealand


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RE: CScolloidal gold.

2002-01-19 Thread I Anderson
Yes Kevin,

But then why go to the trouble of electrically generating ionic gold
when one can purchase soluble gold chloride.

Chemical reduction of gold chloride by various compounds (tannic acid,
sodium citrate, etc.) as you mention is the traditional way of making
commercial and batch quantities of CG, as used in large amounts by the
bio-chemistry industry. With the ability to regulate a uniform
particle size from about 6nm +, it would seem to be the way to go.

Regards
Ivan.

-Original Message-
From: Kevin Nolan [mailto:ken...@optusnet.com.au]
Sent: Sunday, 20 January 2002 3:19 a.m.
To: silver-list@eskimo.com
Subject: Re: CScolloidal gold.


Ivan - suppose one used LVDC and an acid solution to produce ionic
gold
solution. Are there not chemical reduction methods that might not
produce an
acceptably fine gold colloid? I imagine rapid stirring may be needed
when
adding, eg, sodium carbonate (just guessing here). Traditional CG has
been
made that way I think. It would certainly avoid some of the
Frankenstein
HVAC requirements, including it seems boiling the water at times
before
completing a run.

regards, Kevin Nolan



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RE: CSPolarity Switch Experiment

2002-01-19 Thread I Anderson
Sorry Kevin,

You did indeed say:
...a much higher ratio of true CS to ionic silver for the polarity
switched case. Given your faint tyndal effect observations in both
cases, that possibility seems to be ruled out.
which is the opposite to what I said you said.

Ivan.

 -Original Message-
 From: Kevin Nolan [mailto:ken...@optusnet.com.au]
 Sent: Sunday, 20 January 2002 2:45 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CSPolarity Switch Experiment


 With all respect, Ivan, I think you should read again what I
 actually said.

 regards, Kevin Nolan

 Ivan wrote:
 Well it is not the voltage that indicates the rate of silver
 dissolution. The current dip and restoration will be more
indicative,
 and as Kevin mentioned, some of the energy will used in undoing what
 was done in the last cycle, and as he mentioned later, it is likely
 that a higher proportion of metallic colloid particles are produced.
A
 test of total silver content for both runs would be very
interesting.



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RE: CSPolarity Switch Experiment

2002-01-19 Thread I Anderson
Steve,

As I understand the passage of current in aqueous systems.

The passage of current is wholly dependent upon the movement of ions.
As ions have size and weight, they also have inertia and drag and
therefore will lag the application of potential and change in
polarity. Indeed, with the change in polarity the ions must slow down
and reverse their direction, therefore there will be a moment when no
current flows at all, then a build up in current as the ions reach
their terminal velocity. As this occurs for each change in polarity,
the amount of current that flows per unit time is necessarily less for
switching circuits than for non-switching circuits.

I dare say it is not the resistance that changes in your solution
(after all, the number of ions is the same) but rather the current,
and this is the reason you notice a changing voltage.

Regards
Ivan.

 -Original Message-
 From: S  J Young [mailto:you...@konnections.net]
 Sent: Sunday, 20 January 2002 2:16 p.m.
 To: *Silver-List* (E-mail)
 Subject: Re: CSPolarity Switch Experiment


 Ivan,

 Remember my generator produces a constant current, so the
 current can't dip
 at reversal.  Instead, the voltage goes up to maintain the
 constant current.
 In other words, the solution's apparent conductivity goes
 down (resistance
 goes up) for a few seconds at reversal.  Or, the coatings on
 the electrodes
 behave like semiconductors (partial diodes) for a while until they
are
 restructured.  I don't have a clue what is happening at the
 atomic level.
 Perhaps the ions just get confused at reversal, wander around
 haplessly for
 a while wondering why they are suddenly going the wrong way
 on a one-way
 street , they get reoriented again??

 --Steve


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RE: CSPolarity Switch Experiment

2002-01-19 Thread I Anderson


 -Original Message-
 From: Trem [mailto:t...@silvergen.com]
 Hi Ivan,

 We had AA testing done on samples from our SG6 which does not
 have polarity
 reversal and also on our SG7 which does reverse polarity and
 found both
 units produce about 85% ionic.  Apparently it makes no
 difference...at
 least in our units.

 What now?

 Trem

Well, that sort of destroys that theory, Trem.
What now?
Beats me...

BTW, do you need a longer brewing time switched vs. steady, per unit
concentration?

Ivan.


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RE: CSquestions: stir vs. bubble

2002-01-19 Thread I Anderson

Connie and Gaston,

Thanks for taking the time to do those tests and post the results.

It is obvious that at least some increase in conductivity is found as
a result of bubbling.
 It could be, as you add silver ions then further CO2 may be
dissolved, but whether it is worth finding out, I don't know.
In any event, we now know a little more than we did before!

Regards
Ivan.


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RE: CSquestions: stir vs. bubble

2002-01-18 Thread I Anderson
Connie,

A couple of thoughts come to mind:

The stirrer does not mix too well.
You are trying for too high a concentration.
The bubbler introduces CO2 gas to the water, which will ionise and
give a false (high) reading.

If you are finding a change in the CS when exposed to light then it is
possibly due to the quality of your water.

Regards
Ivan.


 -Original Message-
 From: Connie [mailto:wufn...@stargate.net]
 Sent: Friday, 18 January 2002 11:48 a.m.
 To: silver- list
 Subject: CSquestions: stir vs. bubble



 I have the SG6-very happy with my generator.
 I have done some experiementing with the way I make my CS.

 I would like to compare my brew with stirring vs. bubbling and
please
 comments as too the differences.

 I use a 64 fl. oz. coffee creamer container to make my CS.

 Some days...using the stirit seems to take longer. Not
 observant enough
 to say why one day is different vs. another.

 Here are the comparisons of the last two batches made:

 --First brew:
 Stirred batch.
 Seeded, ppm per Hanna PWT 4ppm.
 I cleaned electrodes (with heavy build up) 3 x's during the brew.

 After 36 hours of generation...the ppm per Hanna was about
 18ppm. Indicator
 light, indicating that the brew had not reached 20pppm (as
 dialed) was still
 on.
 My stirred CS ALWAYS reads a lower number the next day, when
 retested. Often
 I will turn the generator back on, let it run again until the
 indicator
 light goes off.

 Allowed the brew to sit overnight. A lot of precipitate in
 the container.
 Did not bother to retest the ppm. ( I expected it to be lower
 than what
 measured the night before)
 I gave up on that brew...used it in the bathwater

 --Second brew:
 Bubbled batch-stirrer removed.

 Seeded DW ppm at start 4ppm.
 10 hrs. later: indicator light off.
 I did not clean the electrodes at all.
 I shut down the generator.
 Did not test the ppm.
 left til this AM, testing ppm with Hanna, the ppm is 26ppm.
 (set at 20ppm)

 Some, but little precipitateelectrodes with little build up.


 My observed main points

 -bubbled CS consistently more stable after brew sits (ppm's
 do not fall from
 one day to the next)
 -bubbled CS consistently has less build up on the electrodes, less
 precipitate in the container.
 -bubbled CS consistently able to achieve higher ppm (per Hanna)
 -occassionally will get pale yellow CS with stir, never with bubbled
 -consistently stirred CS will turn ashen with even minimal exposure
to
 light, bubbled does not seem to (I have not specifically
 ''tested'' this.)
 -brew time for higher ppm's consistenly quicker with bubbler.
 (this case 36
 hours for less than 20ppm stirred vs. 10 hrs. for 26ppm bubbled)

 I have no clue why such a difference. I know Ole Bob you do
 not like the
 bubbler, I believe also Trem that you prefer stir

 Could someone explain some of these differences for me...in
 terms I could
 understand
 and if bubbling is not good, whywhen it appears to make a better
 product?

 TIA
 Connie


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CSSatchid's current schematic

2002-01-16 Thread I Anderson

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  attachment: SatchidGen03.gif

CSRE: cs generator as it is now.

2002-01-16 Thread I Anderson
Yes Satchid, that came through... very nice, thank you.

Couple of questions.

Can you name a substitute for the 4N45 opto-isolators, can't get them
here in NZ.
What type of OPAmp.
Does R3 = 18ohm.
What power supply do you use.
What does R9 control? R11 and R23?
Can you name the TP's for me?

Thanks
Ivan.

 -Original Message-
 From: Satchid [mailto:satc...@sevaproductions.com]
 Sent: Wednesday, 16 January 2002 8:02 a.m.
 To: i...@win.co.nz
 Subject: cs generator as it is now.



 I give you what I have. if you know electronics then it will
 be easy for you
 to understand the setup.


 the first step controls the current,
 the second step the voltage.

 I hope that you can get it in the list.

 The schematic is here

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CSHow to use Beta Glucan

2002-01-16 Thread I Anderson


http://www.alphazee.com/beta-glucan/beta.html
http://www.alphazee.com/beta-glucan/bg.html

Beta 1, 3 D-Glucan Complex

--
--
Biologically active Beta 1, 3 Glucan is actually a complex of beta 1,
3 glucan (about 70%) and other glucan linkages which allows for
polybranching. Yeast derived Beta Glucan with 90% or more carbohydrate
will be good product. Don't get thrown by beta 1, 3 glucan vs beta 1,
3 D-glucan they refer to the same molecule in this regard, one is a
little more discriptive. 99.9% beta 1, 3 glucan is available, it is
produced by bacteria, has no polybranching and is biologically inert,
it is used as a food additive. The controversy surrounding test claims
is discussed below. Lower purity beta glucan(70-75%) can actually be
more bioavailable(more potent) and less expensive but might not be
indicated for those with yeast sensitivity.
--
--

Extensive notes and references on Beta Glucan Complex

How to use Beta Glucan, How much Should I take?
--
--

To: BetaMax Consumers
From: Chip Dopson, ImmunDynamics/Chisolm Biolabs
Enclosed in this packet are the results of our efforts to evaluate and
document BetaMax (beta 1,3 glucan). This was done to further our
knowledge and provide you, the consumer. with the confidence that you
are indeed receiving the most purified and efficacious beta 1,3 glucan
currently available. It is most unfortunate but true, however, that
all current domestic producers of beta glucan with the exception of
us, Chisolm Biological Laboratory, engage in negative discussion
regarding purity and quality of one another's beta glucan instead of
concentrating on improving their beta glucan. We maintain, as has been
our commitment from the inception of our company twenty-two years ago,
to consistently improve our products.

Initially, we inquired from numerous testing laboratories their
capability to test beta glucan. We found they did not have any
knowledge of beta glucan but were quite willing to make an attempt at
testing (this most likely is some of the same labs presently providing
inaccurate or erroneous results). We eventually chose UGA Carbohydrate
Research Center since I was familiar with their capabilities having
graduated from their Organic Chemistry program some years back. This
department ranks in the top ten in the nation and presently the golden
standard worldwide for carbohydrate testing.

I understand our competitors stated the purity of beta glucan
presently available is between 30% and 50% and theirs is 95% to 100%
pure. As you note on UGA's study (February 1997), our beta glucan is
documented to show a total of 94.3%. UGA, however. has created much
confusion recently since they changed the methodology of testing. This
in effect has decreased tile percent results of 1,3 glucan. You will
note that the results from 1997 to 1993 show an increase in
terminal-link glucose and a corresponding decrease in 1,3-link glucan.
Could this increase in terminal glucose be from the direct degradation
of beta 1,3-link glucose? Could higher terminal link glucose mean
higher branching which is indicative of higher immunological activity?

These questions are presently difficult to answer, and only time and
research will provide the answers. UGA stated to us that with the
employment of the new methodology, the results of the 1,3-linkage of
the beta glucan samples was 80% or below. In light of these results, I
can only assume although all current beta glucan producers have had
UGA evaluate their material that they are quite embarrassed to provide
consumers with their lower-than-hyped results. We lay the results out
on the table, and they are what they are. It is unfortunate that the
competition seemingly cannot deal with honesty- UGA also states the
linkage study can vary 5% in either direction on repetitive testing of
the same sample or in essence a 10% error.

I think the important issue for you, as a consumer, is to look at the
composition studies, which relate to the percent carbohydrate and
percent protein of the total sample- You will note that sample #1 (a
production sample from a 250-kg lot) shows 99.9% carbohydrate
(glucose) and a trace protein (0.1%) This denotes that in essence
there is practically 100% link-glucose and only a trace of protein
(yeast extracts and/or contaminants). Yon can also see on the gas
chromatograph only very specific peaks, which represent the various
glucose (1,3 linkage; 1,6 linkage; 2,3 linkage; 3,6 linkage, and
terminal glucose), with very little extraneous material between the
peaks. This data clearly and undeniably proves the purity and
excellent quality of our product.

Thank you.

Summarized Test Results:2/19/97  2/18/98  2/18/98
   #1   #2
Composition analysis:
Glucose 

CSVaginal Yeast Infections.

2002-01-15 Thread I Anderson
My ex was a nurse consultant in the sexual health field. She would
tell her clients (off the record) to use colloidal silver for vaginal
yeast infections, as it worked so well. A spray bottle seemed to be
the preferred method of administration.

Ivan.

 -Original Message-
 From: Craig Chamberlin [mailto:c...@itsmyplace.com]
 Sent: Tuesday, 15 January 2002 5:43 p.m.
 To: silver-list@eskimo.com; Terry Chamberlin
 Subject: Re: CStainted well


 Terry,

 Have you used cs to treat vaginal yeast infections?

 Regards,

 Craig Chamberlin


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RE: CSBill Briggs letter

2002-01-15 Thread I Anderson
I think Kevin read this book, and was somewhat disappointed.

Seems to be an awful lot of mumbo jumbo in this message.
Not quite sure why one would align the water magnetically when one
passes a relatively huge current through it later, or maybe that is
what he means.

Specific ion measurement = conductivity or TDS
Hydrogen potential = pH
Atomic absorption analysis = Atomic Absorption Spectroscopy
Particle charge intensity + or - = ions or sludge?

I didn't realise silver was a co-enzyme, ground breaking research? I
think I remember Kevin mentioning a lack of references in this book.

When prepared in the proper
 manner, silver colloids are capable of achieving these
 reactive tasks in a safe natural manner without side
 effects.

Yes that is true. And fortunately applies to a very wide range of
generating parameters, from the simple battery model to the HVAC
machine.

It tend to agree with your comments Terry.
Is there a reason for making it appear to be really difficult...

Ivan.



 -Original Message-
 From: Terry Chamberlin [mailto:tcj...@yahoo.ca]
 Sent: Tuesday, 15 January 2002 2:45 p.m.
 To: silver-list@eskimo.com
 Subject: CSBill Briggs letter


 Listers,
 I ran across this email in my files from a Mr. Bill
 Briggs to a friend of mine. It seems to me that there
 was some discussion on the list about Mr. Briggs'
 ideas.

 From: Magic Chef Pty Ltd magicc...@bigpond.com
 Subject: SILVER COLLOID AUSTRALIA

 Dear ,

 In response to your email of 8th November I confirm
 that I have written a book titled Silver Colloid The
 True Picture  In this book I give a more informative
 view of silver colloid including x-rays and
 photographs of silver colloid produced in the market
 place today.  The book also confirms the long term
 effects of using an improperly prepared colloidal
 silver.

 I am aware that many manufacturers when they test for
 purity only test for the purity of the silver - e.g.
 particle size, concentration and other metals.  This
 only touches the surface of the purity aspect.
 Testing for purity should also include many other
 tests such as specific ion testing [anyone know what
 he is referring to?] and then compared to atomic
 absorption analysis, hydrogen potential monitoring
 [what? pH?], particle charge intensity [are these real
 scientific terms? Ivan?] and whether it is positive
 (loss of electrons) or negative (gaining of electrons)
 through the electrolysis process. [So far, it sounds
 to me like scientific-sounding gobble-de-gook]

 It is always essential to remember that the greatest
 potential of silver resides in its ability to act as a
 co-enzyme as well as a catalyst. [I'd love to see the
 research data on this]  When prepared in the proper
 manner, silver colloids are capable of achieving these
 reactive tasks in a safe natural manner without side
 effects. [Argyria?]

 For your information production time from preparing
 the water [heating it up?] and aligning the water
 molecular matrix [setting it on a magnet for awhile?]
 to a completed batch of 5 litres takes approximately
 90 minutes and a further 10 minutes for product
 analysis and Q.C. testing.  Then and only then can the
 batch be dispensed.

 Regards,

 BILL BRIGGS

 Terry comments:
 I'll have to admit, when someone describes a process
 that I consider myself familiar with in terms
 completely out of my frame of reference, I conclude
 that he is either conning me, or is a genius I can't
 keep up with. When he implies that CS must be made
 just right (the way he is making it) or suffer side
 effects, my conclusion isn't in the genius category.

 Terry Chamberlin

 __
 
 Web-hosting solutions for home and business! http://website.yahoo.ca


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RE: CSpolluted water

2002-01-15 Thread I Anderson
Satchid,

Do you have a holding tank for your water? This would be the ideal
place to either generate CS in situ, or to add premade CS. Your
generator design (still awaiting schematic ;-) ) would be perfect for
generating in situ, assuming it resets itself when the concentration
drops as fresh water is added. It is lucky that the ionic content of
the water is so low to allow this, (although such a low dissolved
mineral content is unusual). You could then do a series of challenge
tests to determine the lowest concentration required to make the water
sterile.

Having said that, it may be just as easy to pump the well water
through a 0.2um (micrometre) filter, which will remove bacteria, or
use a reverse osmosis filter (but this is wasteful of water). UV
sterilisation or ozone sterilisation might be other options worth
considering.

Regards
Ivan.

 -Original Message-
 From: Satchid [mailto:satc...@sevaproductions.com]
 Sent: Tuesday, 15 January 2002 1:14 p.m.
 To: silver-list@eskimo.com
 Subject: RE: CSpolluted water


 sorry for the mistakes in the spelling, I repeat:



 Dear researchers,

 2 months ago we had a well drilled 40 m deep. The geological
 institute in
 Brussels told us that there would be good drinkable water
 without treatment
 (Before starting to drill). Now the tests from the laboratory
 revealed that
 there is very bad bacteria (even bacteria that could kill
 someone) in the
 water. This is because the well is about 50 m away from a
 canal built for
 boat traffic about 100 years ago.

 There are very little or no salts in the water, the ion
 contend is 1.5 ppt.
 This well was very expensive to drill. Therefore we want to use it.

 Would an injection of ionic silver be able to make the water
 drinkable?

 If so, How would I proceed to do this? Would it be better to
 make the cs in
 the water stream in real time or inject premade cs in the water?

 I will appreciate every suggestion.


 Willy.



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RE: CSpolluted water

2002-01-15 Thread I Anderson
Oh, low iron content ;-)
That makes more sense...and means you would need a timed switch for
the generator, or a reed switch to sense water flow.

Looking forward to seeing the schematic... it is getting more
sophisticated by the minute.

I believe the gold electrodes should be held by a floating assembly,
old Bob' may be able to help you here.

Regards
Ivan.

 -Original Message-
 From: Satchid [mailto:satc...@sevaproductions.com]
 Sent: Wednesday, 16 January 2002 1:45 a.m.
 To: *Silver-List* (E-mail)
 Subject: RE: CSpolluted water


 I am sorry for mi miss spelling of iron. It is an Iron
 content not an Ion
 content.
 Will send you the schematic soon. I am still purifying it.

 I am now working to ad the electronic polarity reversal
 system on it. I made
 a pint of sc with polarity reversing  (by means of a time relay that
 switches over every 40 seconds). The quality is good clear as
 normal water.
 No need for cleaning the electrodes hens no extra dirt from
 the cleaning
 material that could stick to the electrodes. An other point
 that I have
 noticed is that the taste is better, Les bitter after taste.

 I am still locking for a way to make a HVAC unit. I know
 already that I have
 to use a neon High voltage transformer, but I know noting
 about the setup.
 Is it just to put 2 Gold electrodes in the water and apply
 the high voltage
 to it?

 Thank You all.

 Willy



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CSSilver concentration estimate

2002-01-12 Thread I Anderson
I thought message I sent elsewhere would be useful here!

Joe, if you calculate the resistance of the water at the start
(Voltage in volts divided by current in Amps -for those that don't
know), and divide this by the resistance of the water at the end...
then multiply the result by 1.3, you will have a fairly good estimate
of the concentration of silver ions.

In the run below:
start = 75V/0.00377A = 19.9KOhms
end   = 19V/0.00599A =  3.2KOhms

19.9/3.2 = 6.22

6.22 x 1.3 = 8.1ppm as silver ions
Maybe another 1 or 2ppm as metallic silver.

This formula might be of use to quite a few people... don't know why
it didn't occur to me before! Ole Bob might like to refine the
constant further, as he has documented more silver runs than anybody
in the modern world.

Regards
Ivan.


 Hi from Joe:

 Did the following:

 1/9/02  distilled H2O @ 74 F,  short ckt current = 6.38 mA,  supply
 source = 172 + or - 2 Vdc,   R = 26 K ohms   [limiter]  T = elapsed
 time, min.Ve = electrode voltage Ie = electrode current
 electrodes - 5 sq inches submerged on +, 6 sq  on -;  spacing =
2.25
 continuous mechanical stirring


 T Ve Ie
 - 1730
 0  753.77 [calculated - analog meter stuck]
 .5 733.85 
 1  733.85 
 2  71.9  3.88 
 4  703.96 
 6  693.99  [measured -  all following]
 8  674.03
 12 654.13
 15 644.24
 20 604.40
 25 584.47
 30 554.56
 35 524.67
 40 504.74
 45 484.81
 50 464.95
 55 445.03
 60 425.10
 75 365.33
 90 315.51
 105275.57
 120255.71
 135235.72
 150225.73
 165215.77
 180205.95[3 hrs]
 195206.02
 210195.98
 240195.98  [4 hrs - variation due to 120 Vac changes]
 270196.00
 30018.7  6.05   [5 hrs]
 360196.02
 420195.96
 48019.7  6.02
 54019.7  5.97
 600195.99   [10 hrs - end]


 What is your best guess at ppm concentration?

 Thanks.

 ---~-


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RE: CShelp in getting 20mA when converting 220 AC to 110 DC

2001-12-24 Thread I Anderson
Hi Reid,

I think that you are correct, that the resistance of the water and
distance between electrodes will limit the current, at least at the
beginning of the run. If your colleagues are saying that this will
cause your unit to shut down, then you may need a shunt resistor
across your electrodes or a resistor in series with one electrode.
Remember that current = voltage divided by resistance. As your supply
will be constant voltage (correct me if I am wrong, somebody), then
the only way to limit the current is to vary the resistance.

Ivan

 -Original Message-
 From: Reid Harvey [mailto:ceram...@bol-online.com]
 Sent: Tuesday, 25 December 2001 7:50 p.m.
 To: silver list
 Subject: CShelp in getting 20mA when converting 220 AC to 110 DC


 CS Friends,
 In the process of fabricating the electrical component for a new CS
 generator we are running into problems, and seek the help of
 those here
 who are knowledgeable.  The generator design is after what Terry
 Chamberlain has so graciously supplied the list, bearing in mind
we're
 working to stay down to 20 miliamps, as specified by Ole Bob.

 We are having no problem converting 220 volts AC (the standard here
in
 Bangladesh) down to 110 DC, but cannot figure out how to support the
 20mA, without converting by means of a lot of additional apparatus.
I
 had thought that the amount of water, about a gallon, and the five
 inches between the electrodes would bring the amperage down to what
we
 want, but my Bangladeshi friends are telling me this cannot happen
 without the system shutting down.  Can someone help us to understand
 what to do.  I feel sure we are simply missing some small piece of
the
 puzzle.
 Thanks.
 Reid



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RE: CShelp!

2001-12-20 Thread I Anderson
Hi Jim,

I saw your original post, and made a note to have a look at it later
and filed it in the too hard basket.

The trouble is with 36 volts and no current limit probably 15ppm will
be the limit before things start getting murky and grey.

What I suggest is that you run with 36V until you hit 3mA. That will
probably take about 2 or 3 hours and give about 10ppm. Drop your
voltage if you can to 18V for another hour which should be around
15ppm. Drop the  voltage again to 9V for another hour for 20ppm.

Another way to look at this is by resistance.
Your starting resistance is E/I = 36/.00022 = 164,000 Ohms
You want a twenty-fold increase in conductivity (or there a bouts) so
you need a twentieth of the resistance...which equals about 8200 Ohms.
This may be a little on the low side but equates to a current of about
4.5mA.
If you can get to this without large amounts of sludge (may well be
possible) then do so. If, on the other hand you do start getting
constant fluffy coating of the anode, then wipe it off and drop the
voltage.

Good luck to you,
Ivan



-Original Message-
From: Acmeair [mailto:res00...@gte.net]
Sent: Thursday, 20 December 2001 8:23 p.m.
To: silver-list@eskimo.com
Subject: CShelp!


i've just made a 3 unit adapter, 28vdc unit, using 2 silver rounds, on
12 ga .999 wire for a friend.  we just tried his unit out on monday.
it worked as advertized.

this morning, he called, and was asking wether or not CS worked on
Ebola. wow!  i told him that according to beck's writings, and stuff
on this site and others, i was of the impression that it did work on
ebola. why are you asking, i said.??  this guy has been heppin out an
older guy, and his wife. she was having trouble with her feet, and had
gone to the hospital with what looked like gang green. the AMA doc's
couldn't figure out what was going down. they finally informed the
family that the lady had something that was similar to ebola, but was
not in fact ebola. woweee!!

i have asked for some help on this site,  regarding how much current ,
and time, etc. it takes to make 15-20 ppm cs with my unit. i'll cut
and paste my first request.  i'd sure like to know if i'm making cs at
a proper strength to hep.



just finished bumping my cs unit to 3 6 vdc adapters in series, giving
me 29.5 vdc. with 31 oz of DW  @ 62 degrees F, the initial flow is .22
ma. with the elements 1 7/8  apart. the wetted area is about 2.85
square inches.  (using one 14 ga wire, and one silver round hung on 14
ga wire.  at what milliamps would i be gettin 15-20 ppm?   thanks
a lot.  jim O+, S 

would deeply appreciate any hep, or data.   thanks,jim O+,
S


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RE: CSWater Distiller

2001-12-20 Thread I Anderson
Hi there Ted,

Trouble is, there is quite a difference between tap water which
carries high concentrations of dissolved solids already, and steam,
which is pure water looking for solids to dissolve. Steam is quite
reactive and corrosive, and will eat away at the copper tubing.
Perhaps some plastics might be alright especially those that can
withstand autoclaving.

Ivan

 -Original Message-
 From: Theodore Corbett [mailto:miesenbac...@yahoo.com]
 Sent: Thursday, 20 December 2001 10:17 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CSWater Distiller


   I don't see a reason why you couldn't use copper
 tubing as long as your distilling drinking water. In
 my house the plumbing for the hot and cold water is
 copper pipe. I just recently tested my water and one
 of the tests was for copper and the test came out
 negative and the copper pipe is at least 15 years old!
 If you go to one of the home brewing supply houses on
 the web they sell 3/8 and 1/2 coiled copper tubing
 that would be perfect for a distiller. They use them
 to cool the wurt when brewing beer. They run between
 $20.00 to $50.00. They also have high temp plastic
 tubing. If you need a couple URL's for the home brew
 sites let me know. Ted Corbett


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RE: CSRequest

2001-12-20 Thread I Anderson
Time for another 'Chateaux Pomeroy's' Brooks.

I think you might be meaning Alvin Rose you should be able to reach
him at:
 i...@rtvc-2000.com

Merry Christmas to you also, and many more!

Ivan.


 -Original Message-
 From: Brooks Bradley [mailto:liat...@flash.net]
 Sent: Friday, 21 December 2001 4:26 p.m.
 To: silver-list@eskimo.com
 Subject: CSRequest


 I have just...todaygotten my PC system
 cleaned and back
 up.  It was necessary to purge everything in my mail systems
 and during
 the process I lost all of my mail archives---for both
 mailers.  The net
 result was I have lost all of my mail records for the past six
 months..both inand out.
 Recently, I mailed some benign...but
importantchemical
 to Alan Rose in Canada.  If anyone on the list happens to
 have his email
 address I would be more than appreciative for same.
 Alan, if you are listening...please send it
 to me.  I am
 most anxious to see if you have received my promised mailing.
  Since my ISP mail back-up contained over 1500 messages,
I
 have been rather busy editing this evening.
 She-Who-Must-Be-Obeyed (wife), daily
 reminds me I need
 a 24 hour keeper and should not be allowed to mix with the more
 Web-Literate young folk...such as frequent this list.
 Obstinance
 being my principal claim to intellectual substance..I refuse to
 surrender this last vestige of personality announcing my worth to
the
 planet.
 Additionally, since destiny may not grant
 me another
 Christmaspast this oneI hope list protocol will indulge my
 wishing each of you only the most joyous experiences during
 this holiday
 season.
 Sincerely,  Brooks Bradley.


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RE: CSRe: concentrated CS and 'aglomeration'

2001-12-19 Thread I Anderson
Kevin,

I was trying to show that it is not the salt but the silver load that
may cause argyria or other problems. Most salts are absorbed as
dissolved ions, the cations taking different pathways to the anions.

If a salt was to be absorbed as a compound, then the fact that this is
so would suggest that the salt does not disassociate readily, and
therefore would be less reactive than the component ions. The
difference between compounds and CS is the concentration at with they
are supplied. It matters only that free silver ions are available to
react with body tissue, and the number of ions that do so.

If several different salt solutions, containing the same
concentrations of free silver ions are tested against microbes, I
would expect the results to be similar, disregarding the effect the
anion may have.

In aquatic environments, waters which have high sulphide or chloride
conditions, high silver concentrations have little effect on
susceptible marine creatures as there is little in the way of free
silver ions, however in places that have a high concentration of
dissolved silver pollution, aquatic creatures can be severely
effected.

I am always wary when someone says that this physical event cannot
occur ;-)
Surely the electrostatic effect of ions in solution is rendered
neutral by the solvation by the polar water molecules, creating large
crystal like structures which are essentially neutral at their
boundary with the bulk solution. I do not think this has been well
investigated, mainly due to the difficultly of forming and capturing
ions of a single species.

Your thoughts good sir?

Ivan.

-Original Message-
From: Kevin Nolan [mailto:ken...@optusnet.com.au]
Sent: Tuesday, 18 December 2001 2:15 p.m.
To: silver-list@eskimo.com
Subject: CSRe: concentrated CS and 'aglomeration'


In digest #1195, Ivan anderson wrote, in two separate postings:

If a silver salt or protein were to enter the body as a compound,
then it is much less likely that it will be deposited in the tissue,
simply because the compound must have a high affinity for the silver
and would be far less reactive. This is why silver salts and proteins
have less germicidal effect in the test tube than silver ions.
However, because these compounds are often supplied at very high
concentrations, the available silver ions (while small as a percentage
of total dose) may in fact be large enough to cause some deposition in
tissue.

The term 'salt' should really only be applied to the solid
compound. When a salt is dissolved it ceases to be a compound and is
then a aqueous mixture of the two separate and distinct ions from
which it was formed. Silver hydroxide, when dissolved, is simply
silver ions in slightly more alkaline water. The same applies to
silver nitrate, which completely dissolves at very high
concentrations. The silver is available as silver ions, as is the
nitrate. Unfortunately, the nitrate is corrosive to tissue It is
most likely not the species that the silver ions are derived from that
can cause problems, but rather the concentration in which they are
present.

Leaving aside organic silver compounds and mild silver proteins, there
seems to be a contradiction between the first and second quotes above,
in relation to salts vs ions. We agree that whether as a silver salt
such as silver nitrate, or (as Marshall Dudley would point out) a base
such as silver hydroxide, when dissolved in water such ionic compounds
dissociate fairly well completely to give just a mixture of ions. How
then can it be said that dissolved silver salts are much less
effective than silver ions? Are they not in effect one and the same? A
while back I pointed out it is impossible to have just one ionic
species in solution - charge neutrality requires that ionic silver (or
any other cation) must always be accompanied by anions of some kind,
whether hydroxyl, nitrate, acetate or whatever.

This brings the matter back full circle. Despite all the words so far,
the following basic issue has not been answered:
Suppose we have different ionic silver compounds each made up to the
same PPM dissolved silver ion in solution. Examples might be 10PPM
silver each as silver hydroxide, silver acetate, silver citrate,
silver bicarbonate. For none of these is the anion either poisonous or
germicidal. Should we expect the germicidal power to be essentially
equivalent, whether in the test tube, or in the body? If not, on what
basis?

regards, Kevin Nolan ken...@optusnet.com.au


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RE: CSRe: concentrated CS and 'agglomeration'

2001-12-19 Thread I Anderson
That is correct.
Indeed, CS of high ionic content (85%) and small size particle
remainder is colourless and has very little TE. One may even have to
go into a dark room to see it.

Ivan

 -Original Message-
 From: Jonathan B. Britten [mailto:jbrit...@cc.nakamura-u.ac.jp]
 Sent: Thursday, 20 December 2001 8:09 p.m.
 To: *Silver-List* (E-mail)
 Subject: Re: CSRe: concentrated CS and 'agglomeration'


 I take this response to mean, then,  that all of the Tyndale effect
I
 observe using a ruby laser pointer is based on actual particles of
 silver, and not of silver ions. I would assume then that
 any product
 consisting of 100% siler ions -- if such is possible to make --
would
 have no Tyndale effect, even with a laser beam.   Is that correct?

 Thanks in advance.

 JBB



 I Anderson wrote:
 
  You are correct JBB, in a manner of speaking, but the wavelengths
of
  'light' that are small enough to be reflected are not visible.
They
  are in the ultraviolet and the x-ray range.
 
  Regards
  Ivan.
 
   -Original Message-
   From: Jonathan B. Britten [mailto:jbrit...@cc.nakamura-u.ac.jp]
   Sent: Tuesday, 18 December 2001 1:21 p.m.
   To: *Silver-List* (E-mail)
   Subject: Re: CSRe: concentrated CS and 'agglomeration'
  
  
   Well, what if you get lots of ions all together in one jar?
   Would not
   certain wavelengths of light bump into some of them?
   Honestly I do not
   know,  but it seems possible.
  
   JBB


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RE: CSRe: concentrated CS and 'aglomeration'

2001-12-15 Thread I Anderson
Reid,

The term 'salt' should really only be applied to the solid compound.
When a salt is dissolved it ceases to be a compound and is then a
aqueous mixture of the two separate and distinct ions from which it
was formed. Silver hydroxide, when dissolved, is simply silver ions in
slightly more alkaline water.

The same applies to silver nitrate, which completely dissolves at very
high concentrations. The silver is available as silver ions, as is the
nitrate. Unfortunately, the nitrate is corrosive to tissue.

Gold chloride dissolves as gold 3+ ions and chloride ions. The
chloride is non toxic but the gold ions will oxidise body tissue and
enzymes and can cause problems. Metallic gold on the other hand, has
all its electrons and is quite non-reactive.

It is most likely not the species that the silver ions are derived
from that can cause problems, but rather the concentration in which
they are present.

Ivan.

 -Original Message-
 From: Reid Harvey [mailto:ceram...@bol-online.com]
 Sent: Thursday, 13 December 2001 3:00 p.m.
 To: silver list
 Subject: CSRe: concentrated CS and 'aglomeration'


 Ken,
 I never stopped to think that the silver may be the
 hydroxide, evedince
 that my understanding of chemistry is limited. (Sometimes I stop and
 think and sometimes I just stop.)  Can you fill me in on how
 it is that
 the hydroxide is a salt? Does anybody else have an answer? I feel
sure
 that you're correct that the reason this is not harmful to us
 CS lovers
 in the long run is that 10ppm is extremely dilute.  Of course
 this begs
 a question about assertions here that it's not a problem to
 ingest ionic
 silver at the really high concentrations.  If this sort of CS is
 practically unattainable without the salts then responsible people
 should talk about some kind of an upper ppm limit for
 ingesting.  On the
 other hand finding that number may be difficult.

 Also, back to my limited chemistry, I would like to know why
 it is that
 one would have to isolate one element in a simple compound as the
 culprit in a health problem.  For example with silver nitrate why
does
 the problem have to be either the silver or the nitrate.  I think
the
 problem is probably the compound.  Another example:  it's been
stated
 here that gold chloride is highly toxic, yet gold metal is
beneficial
 and chlorine is a lot less toxic.
 Salaam,
 Reid


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RE: CSRe: concentrated CS and 'aglomeration'

2001-12-15 Thread I Anderson
Jason,

The body reacts to metals electro-chemically. The fate of these metals
depends upon the physical properties they exhibit. Silver will bind to
albumin in the blood plasma, selenides, sulphides, ascorbates,
metaloproteins and so on. Some will inevitably bind to these groups
which may be found in tissue and organs. If the concentration of
silver is high, and the concentration of selenium (for example) is
low, then more silver is likely to bind with tissue. When the bodies
supply of metaloproteins become low, because of their use in binding
with silver (or some other metal) then more are manufactured, if large
amounts are required this may trigger an immune response, a rise in
the white blood cell count, and an increase in body temp.

If a silver salt or protein were to enter the body as a compound, then
it is much less likely that it will be deposited in the tissue, simply
because the compound must have a high affinity for the silver and
would be far less reactive. This is why silver salts and proteins have
less germicidal effect in the test tube than silver ions. However,
because these compounds are often supplied at very high
concentrations, the available silver ions (while small as a percentage
of total dose) may in fact be large enough to cause some deposition in
tissue.

Don't be fooled into thinking that solid food is treated any
differently to liquid food. Food enters the body as ions and
molecules, and water enters as water.

Even when silver was normally supplied as highly concentrated salts or
proteins, only a very small percentage of its users developed argyria.

Ivan.

 -Original Message-
 From: Jason / AVRA [mailto:silverd...@hotmail.com]
 Sent: Thursday, 13 December 2001 3:44 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CSRe: concentrated CS and 'aglomeration'




 From: Kevin Nolan ken...@optusnet.com.au
 But is argyria solely due to the high silver dosage possible
 with silver
 nitrate (very high solubility), or is there some kind of
 synergy effect as
 well?
 regards, Kevin Nolan

 Kevin:

 The slate blue colour of argyria is not entirely due as one
 might suspect,
 to the deposition of metallic silver (Petering, 1976), but
 largely to an
 increased deposition of melanin.

 Apparently, the issue of Argyria ( the two types ), is not as
 simple as it
 may first appear.

 Silver, in any form, when it reaches a certain theoretical
 concentration
 in the body is a toxic substance.  Like most toxic
 substances, the effects
 will only last while the substance is active in the body.
 The question is:
 When and why does silver accumulate in the body, and when and
 why does it
 not?

 The body knows, and responds, to a toxic substance when
 detected in the
 body.  This is a toxic response...  It happens every time one
 eats garlic,
 for instance.  The body moves to remove the substance as quickly as
 possible.  This is a system-wide, metabolic response of the
 body.  This
 response is markedly different than the normal elimination
 responses in the
 body.

 First, I believe that with the colloidal silver that most
 use, the body does
 NOT detect the silver as toxic.  I don't believe the
 concentration is great
 enough, even at say a liter per day.  I believe that isolated
silver,
 whether in ion form or in colloidal particle form, is not
 deposited nor
 accumulated in organs or skin tissue, whether a toxic response is
 experienced or not.

 I believe that some, if not many, silver salts and proteins
 DO deposit
 silver in the tissue, because the body does not handle these
 substances in
 the same manner as it does water.  This is the key concept.
  What is the
 body trying to do with these salts and proteins?

 I can induce a toxic reaction to isolated silver through
 heavy lung use.  If
 the silver accumulated in the organs, then the symptoms would
 continue as
 documented in many materia medicas.  However, the symptoms
 are temporary,
 corresponding very closely with the conclusions drawn in
 Roger Altman's
 informal study on silver elimination.

 However, I believe that even a teaspoon of silver
 protein/salts can easily
 cause a toxic reaction in the body.  I believe this based upon the
 documented cases of Argyria from the old school medical
 documents and the
 EPA listed studies.  When a toxic reaction occurs to these
 substances,
 silver begins to accumulate in tissues.  Obviously, this
 doesn't ( or should
 say 'didn't ) occur in every case, or there would be
 thousands of more
 documented cases of Argyria back then.  Evidently, Argyria (
 to the point
 where it was noticed and recorded ) only occured in a small
 percentage of
 the people using silver-based products.  These people may
 have accumulated
 silver more quickly through vitamin E and Selenium
 deficiencies.  There may
 be other factors involved as well.

 The whole idea here:  One wants the silver product to be
 treated exactly
 like water, not like a food substance or a solid.  That is
 exactly what you
 get with 

RE: CSdr. jon - an update

2001-12-10 Thread I Anderson
Well,
I don't know...

 1.  Dr. Jon Brooks appears to be the pen name of Fred
 Fason, M.D., who graduated from Baylor Medical School
 in 1960.  Dr. Fason did his residency at U.C.L.A.

Is it or not? If it is why does the rest of the letter talk about
Stewart Fason or John Fason? One is a lawyer and one is a doctor, one
gives money away... are they all Dr Jon?

Is there such a person as Dr Jon Brooks retired oncologist, dispenser
of medical advice and vitamins? If Dr Jon is a Fason, is that not
deception.

Wouldn't describing an alias as a pen name require a spin doctor?

This letter does not answer any of the points raised by Hanson and
Miller, and reads more like a PR brochure than an incisive piece of
detective work.

And note the twisted logic, that if Hanson and Miller cannot prove
harm then they are guilty of viscous character assassination (after
all there is a whisper that they are involved in MLM practices and
therefore have no honour or virtue), even while conceding in the same
sentence, that at least some of their claims are true.

When someone builds an empire (be it for profit or not) on the back of
respect gained, as an oncologist who has turned his back on his peers
and embraced alternative treatment. Someone who uses the powerful
legitimacy that this lends to his recommendations, but who is in
truth, someone that is not only not a doctor but is a man who uses
alias to suit his aims, and may in fact know absolutely nothing about
health at all. I'm sorry, but I view this as a pretty serious travesty
of right and wrong. Certainly, people should be given the evidence, so
they might make an informed judgement as to the weight they assign to
the legitimacy of his past and future claims.

Ivan.

 -Original Message-
 From: cking...@nycap.rr.com [mailto:cking...@nycap.rr.com]
 Sent: Monday, 10 December 2001 10:16 a.m.
 To: silver-list@eskimo.com
 Subject: CSdr. jon - an update


 Another look from another list, about the co-op's good doctor.
 I'm glad I didn't jump in and join the slanderfest...

   Chuck
 Transvestite: A guy who likes to eat, drink and be Mary!

 This is a post from another list by Darrell Sandlien,
 concerning the Dr.
 Jon scandal.

 I have followed the well documented allegations made
 by Mr. Hanson and Ms. Miller with great interest.  The
 evidence is compelling that deceptive practices are
 involved.

 I am a retired P.I. and am fascinated by puzzles.

 The facts I have learned, from public records mostly,
 are:

 1.  Dr. Jon Brooks appears to be the pen name of Fred
 Fason, M.D., who graduated from Baylor Medical School
 in 1960.  Dr. Fason did his residency at U.C.L.A.

 2.  Stewart Fason is a well known philanthropist in
 the Palm Beach, FL area.  He donated his home, at 115
 Via la Selva, Palm Beach to The Jewish Community Day
 school.  It had a mortgage of over 300k so the school
 only netted about 650k when sold for $1,000,000.00 to
 a bank president.

 He gave away almost $200,000.00 in computer equipment
 to various schools and universities.

 I spoke with Carol Roberts, a former Mayor of W. Palm
 Beach.  She confirmed that the Fasons presented many
 concerts in So. Florida, showcasing young artists.
 They would invite the entire audience to their home
 for a post concert reception.  They were the first to
 open their mansion to ordinary people.  There was
 never any charge.  They refused to accept any
 donations.

 If one could not afford the modest cost of the
 concerts, they became guests of The Chopin Society, a
 charitable trust founded by the Fasons.

 In the 70's Fason got in a jam with the C.F.T.C.
 After years of litigation he settled for a $75,000.00
 fine, which was peanuts to him.

 3.  There is little data on John Fason.  All I could
 find was he graduated from Rice University Law School.

 My friend was overcharged by $22.00 by the Generic
 Co-op.  Within a week he received a refund check,
 which it appeared Fason signed.  The check was drawn
 on The First National bank of Sharp County, Ash Flat
 AR.

 I called the bank and was referred to Morris Street,
 an officer.  Mr. Street knew John well and had only
 glowing comments.  They handle all the VISA/MC
 business for the Co-op.  I asked if they had many
 complaints about The Generic Co-op.  He replied, Not
 one from thousands of transactions.

 MAKING SENSE OF ALL THIS

 There is no doubt that the Fasons walk to a beat of a
 different drummer.

 In reviewing the past newsletters on Yahoo I came
 across this, allegedly written by his cat ON
 8-26-01???:
 *
 IF YOU BOUGHT BETA SITOSTEROL RECENTLY, YOU GOT
 E-SCREWED!

 The lab report came in today.  It revealed that the
 current production of Beta Sitosterol contains only
 90% of what is claimed.

 To meet the CO-op's specifications it must have a
 minimum of 97%.

 I advised him to just clam up, as you would never know
 the difference for it is still almost twice 

RE: CSRe: Eniva's angstrom sized ionic minerals

2001-12-06 Thread I Anderson
Hi Again Kevin,

You wrote:

Judging from your remark they do not use salt., perhaps you didn't
understand what I was saying by seems to me a simpler definition
would suffice:
Angstrom size ionic mineral = salt (general term, not just NaCl).
Example: silver hydroxide - which is about 80-90 % of the output of a
typical home-made low tech CS generator!

I am not quite sure where the silver hydroxide remark comes form, but
very little in the way of silver hydroxide is formed at pH less than
9. If you are referring to precipitation, AgOH solid is brown.

I was trying to make it clear that it was the general term salt,
meaning any combination of (generally) metallic cation, such as Ag+,
Ca++, etc, and any anion, such as OH-, Cl-, SO4--. When dissolved in
water, such salts dissociate, either completely or partially, to
produce angstrom-sized ions! Eniva are at pains to distinguish their
product as being definitely NOT a colloid, but is both angstrom sized
and ionic. Well if that's not a good definition of a dissolved salt,
what is it? Are they claiming a new state of matter? I requested more
info as per their web site offer, only to receive a strong come-on to
join as a MLM affiliate.

The definition of a dissolved salt requires both cations and anions.
If Eniva can introduce Ag+ cations into the water, without adding
anions, then this is not a dissolved salt. Eniva claim to do this by a
vacuum plasma process.

DG, if you are convinced their product is truly superior, I'd love
to here more from you as to your experience using it. At the moment,
things are not quite adding up.

That would be interesting.

Ivan.


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RE: CSCancer Cure

2001-12-05 Thread I Anderson
Thank you Robb,

Very interesting.

For those that might wish to learn more, the patent no. for this
procedure is US 5,578,637.

Ivan.

 -Original Message-
 From: Robb Allen [mailto:rube2...@hotmail.com]
 Sent: Thursday, 6 December 2001 1:46 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CSCancer Cure


 Here it is

 http://www.msnbc.com/news/667259.asp

 From: Tel Tofflemire telt...@home.com
 Reply-To: silver-list@eskimo.com
 To: silver-list@eskimo.com
 Subject: Re: CSCancer Cure
 Date: Wed, 05 Dec 2001 17:28:21 -0700
 



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RE: CSOzonated water, FIR fibre

2001-12-05 Thread I Anderson

Kevin Nolan wrote:

From what I have read, as soon as ozone hits water it converts to
H2O2 - which I can purchase as 50% technical grade for $1 AU per
litre. How many litres does that work out to as the equivalent cost of
an ozone generator (which needs bottled oxygen, I understand)?

Not so Kevin. O3 will dissolve in water to eventually degrade to H2O2.
O3 will remain dissolved in room temp water for a few minutes and in
ice cold water for  about 20 minutes.
Ozone can be generated using dry air quite acceptably, without the
generation of the nitric acid contaminant that would accompany 'wet'
air.

As for so-called Far infrared fibres - the concept defies basic
thermodynamics. All materials emit and absorb precisely the same
spectrum of heat radiation when at the same temperature. If your FIR
underclothing seems better, either it is simply better at insulating,
or you are experiencing the power of suggestion. Ditto for the FIR
bags - it will be the ozonated CS doing all the work.

Again this is not so, as far as I know. Some elements or compounds
(silicon dioxide, aluminium oxide) will accept energy of some
wavelength and then radiate it at another, in the far infrared in this
case. All that is required is the conservation of energy.
While the same energy is output (more or less) FIR radiation is much
more efficient at heating our bodies as it is able to penetrate deeply
(unlike radiation of shorter wavelength) and is similar to the
resonant frequency of water and tissue and thus the energy is absorbed
more efficiently.

Regards
Ivan.




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RE: CSburning

2001-12-05 Thread I Anderson
I'm over here, Tracy. LOL.

I re-sent the message that I sent you a week ago, which you must have
missed. It has all the info you requested.

Burning...
Why is the baby being given CS. Is there some health problem?
It could be that the entire family is suffering from some sort of
gastro infection or other malady which the CS reacts with.

I suggest you retrieve the CS from these people and try it
yourself...replace it with some that you know is ok, ie you have drunk
a sample yourself. If you do not have a burning reaction then perhaps
the family should have some tests run.

Regards
Ivan

 -Original Message-
 From: Nick Grant [mailto:nwgr...@inet.net.nz]
 Sent: Thursday, 6 December 2001 2:19 p.m.
 To: silver-list@eskimo.com
 Subject: Re: CSburning


 Hi Dean

 Ivan has tested my CS in the past and it has been fine.  I
 used cheap water
 for awhile till I found out that it was a problem, then went
 back to the
 original DW that was a lot more expensive, and  that Ivan had
 tested.  I
 don't put the leads in the water and the wires are fine.  I
 am in the middle
 of getting some more from Ivan as they are pretty worn (thin).

 It doesn't have this affect on anyone else that I give it to.
  My whole
 family drink it and we have never noticed any burning.

 It is a mystery to me.

 I will send some up to Ivan for testing as soon as I hear from him.

 IVAN are you thereYoohooo


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