Re: CSBeck machines

2000-08-09 Thread Ritz3131
In a message dated 8/7/00 6:54:06 AM Pacific Daylight Time, tw...@yahoo.com 
writes:

 I am definitely feeling better, more energy, after
 just a week of following the directions. Also, I have
 twice (the last two days) experienced coming home from
 a long day, very tired, hooking up the Blood purifier,
 and feeling noticeably better ten minutes later.
 
 Terry Wayne 
Good news.  Hope you keep improving.  I forget...what are you using this for?

Thanks,

Christy


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CSdistilled water-cs-have to be made with?

2000-08-03 Thread Ritz3131
This may be a dumb question but does colloidal silver have to be made with 
distilled water or can you use spring water?

Thanks,

Christy


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Re: CSHYPERBARIC CHAMBER

2000-08-03 Thread Ritz3131
In a message dated 8/3/00 3:53:05 PM Pacific Daylight Time, jlay...@ainet.com 
writes:

 Subj: CSHYPERBARIC CHAMBER
 Date:  8/3/00 3:53:05 PM Pacific Daylight Time
 From:  jlay...@ainet.com (Jeff Laymon)
 Reply-to:  jlay...@ainet.com
 To:silver-list@eskimo.com
 
 
 
 
 Bob Squires wrote:
 
 
 colorparam7F00,,/param Dear friends;
 
 
 
  I am studying the creation of
 
  hyperbaric chambers that can be low cost for home use machines . These
 
  may produce great benefits . Does any one have any ideas about them .
 
 
 /color- - - - -  - Thursday afternoon, Modesto California  (real 
hot..power 
 companies sweating bullets)
  
Keep us (and me) informed.  Sounds like a great idea.

Christy


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CSLymesilverCheck out http://www.escape.ca/~revive/burgd.txt

2000-07-24 Thread Ritz3131
 A HREF=http://www.escape.ca/~revive/burgd.txt;Click here: 
http://www.escape.ca/~revive/burgd.txt/A 


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Re: CSLou Gehrig's disease?

2000-07-23 Thread Ritz3131
In a message dated 7/22/00 9:27:39 PM Pacific Daylight Time, 
spiro...@tampabay.rr.com writes:

 
 But a treatment protocol such as the 4-part plan proposed by Robert Beck PhD
 would be my personal choice for dealing with a complex of diseases like Lyme
 or Lou Gehrig's disease. That protocol includes CS, blood electrification,
 magnetic pulsing and drinking ozonized water.
 
 Spiroflex 
Hi.  Forgive my bad memory if you have already posted this but have you had 
personal experience using this protocol and success?

Thanks a lot.

Christy


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Re: CSLou Gehrig's disease?

2000-07-23 Thread Ritz3131
In a message dated 7/22/00 9:27:39 PM Pacific Daylight Time, 
spiro...@tampabay.rr.com writes:

 
 I found an abstract of Mattman's report on the Web at PubMed Web at:
 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9861561form=6db=m;
 Dopt=b
 
 If you cannot access this, let me know and I'll post it. 
Hi.  I can't access this site but would like to see it if you can post it.

Thanks,

christy


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CSNicole Buring in nose OT

2000-07-23 Thread Ritz3131
Hi Nicole,

Was going through some old emails.  I have heard the burning in the nose is a 
symptom of babesia.
  I hear artemesia (worm wood) helps.  At first may increse the burning but 
then decreases it.  I have been taking it in case I have babesia as 
peripheral blood smear said suggestive of babesia but I think It has been 
increasing my estrogen...am having premenstrual cramping again and toe pain 
as I did pre-antibiotics for Mycoplasma fermentans incognitus which we think 
estrogen makes worse.
Christy


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Re: CS for Fibromyalgia?

2000-07-21 Thread Ritz3131
In a message dated 7/20/00 4:48:39 PM Pacific Daylight Time, 
writety...@aol.com writes:

 Subj: Re: CS for Fibromyalgia?
 Date:  7/20/00 4:48:39 PM Pacific Daylight Time
 From:  writety...@aol.com
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 The battlefields in the Gulf War are now covered with literally
 TONS AND TONS of radioactive bullets that were used.  Any
 possible correlation to health problems vets have had?
 
 Frank 
Yes


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Re: CS for Fibromyalgia?

2000-07-20 Thread Ritz3131
HI There,

I was wondering what the dose is you are taking of MSM.

Thanks,

Christy

In a message dated 7/18/00 8:52:57 PM Pacific Daylight Time, 
quiksa...@home.com writes:

 Subj: Re: CS for Fibromyalgia?
 Date:  7/18/00 8:52:57 PM Pacific Daylight Time
 From:  quiksa...@home.com (Quiksassy)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 I have fibromylgia and the chronic fatigue with it.  I recently started 
taking MSM and I feel so much better.  I have alot more energy.  I am on a 
medication wellbutrin which helps with the pain and has let me get some 
rest.  I have read that it is the lack of being able to get deep sleep which 
causes alot of problems associated with fibromylgia.  I am a patient with one 
of the leading doctors in the country at Georgetown Hospital.  He is taking a 
leave for a year to research the gulf war illnesses.   One of the problems is 
that many people have developed fibromylgia.  Good luck 


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Re: CS for Fibromyalgia?

2000-07-20 Thread Ritz3131
In a message dated 7/19/00 9:17:16 AM Pacific Daylight Time, 
mdud...@execonn.com writes:

 Subj: Re: CS for Fibromyalgia?
 Date:  7/19/00 9:17:16 AM Pacific Daylight Time
 From:  mdud...@execonn.com (Marshall Dudley)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Check http://dorway.com/ for information on aspertame poisoning.
 
 I know that I saw a comparison of the known symptoms of aspertame
 poisoning and Gulf War syndrome, and the list was identical from end to
 end.  Fact is that Coke sent loads of diet drinks over there, and they
 sat in the sun for weeks making methyl alcohol, before being drunk by
 the thousands.  It was completely predictable, and since the symptoms
 completely match, almost for certain that is the cause.
 
 I will try to find that reference.
 
 Marshall
 
 Katie Jay wrote:
 
  Hi Marshall, I was told my mycoplasma infection was the cause of my
  Gulf War Syndrome. Do you have any further information about
  aspertame being the culprit? Thanks,Katie
  
I think the ONLY thing that the government is telling the truth about 
regarding GWS is that there is no single cause.  The aspartame I am sure can 
cause problems but it does not explain transmission to family members and 
pets.  See www.gulfwarvets.com.

Christy


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Re: CSViolet Ray

2000-07-14 Thread Ritz3131
In a message dated 7/11/00 12:22:36 PM Pacific Daylight Time, 
mdud...@execonn.com writes:

 Subj: Re: CSViolet Ray
 Date:  7/11/00 12:22:36 PM Pacific Daylight Time
 From:  mdud...@execonn.com (Marshall Dudley)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Actually what I have been hearing is that they are like a minature Rife 
machine.
 Cayce recommend their use in many of his readings.  I have a friend that 
said that
 he was able to kill toothache in a matter of seconds with one.  I am 
thinking they
 might induce a magnetic field and current in tissue, and thus act like a Rife
 machine, zapper, magnetic pulsar, or TENs unit, or a combination of these.
 
 If I get any more information I will let you know.
 
 Marshall 
Keep us posted.  Sounds interesting.

Christy


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Re: CSBob Beck machines

2000-07-14 Thread Ritz3131
In a message dated 7/13/00 8:40:28 PM Pacific Daylight Time, 
dotsie...@aol.com writes:

 Subj: Re: CSBob Beck machines
 Date:  7/13/00 8:40:28 PM Pacific Daylight Time
 From:  dotsie...@aol.com
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 In a message dated 7/13/00 2:43:47 PM Eastern Daylight Time, 
 bradki...@webcombo.net writes:
 
   You have to use
  bloodelectrification in one word for it to work. it seems like they are
  trying to hide it. 
 Hi Brad,
 
 When I started the bloodelectrification list last year, I was having a 
 difficult time finding information/testimonials from people who actually 
used 
 the Beck protocol and was hoping that someone else would start a list - no 
 such luck. At the time, I didn't know what to name it but I am always open 
to 
 suggestions.  I agree, it's a little confusing.
 
 Dotsie 
 List Moderator - bloodelectrificat...@egroups.com 
How do you join the list?

Thanks,

Christy


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Re: CS for Fibromyalgia?

2000-07-14 Thread Ritz3131
Fibromyalgia may be actually Mycoplasma fermentans incognitus 
(www.immed.org, www.gulfwarvets.com) or Lyme so I would give the cs a try.  
If she wants blood work done first to find out what is causing the 
fibromyalgia she should have her blood drawn prior to testing b/c for 
example with the M. fermentans incognitus being on antibiotics can cause a 
false negative.

Christy

In a message dated 7/13/00 9:01:00 PM Pacific Daylight Time, 
you...@konnections.com writes:

 Subj: CS for Fibromyalgia?
 Date:  7/13/00 9:01:00 PM Pacific Daylight Time
 From:  you...@konnections.com (Steve Young)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com (Silver List)
 
 Perhaps this is a bit off topic.  My wife suffers from fibromyalgia and has 
not found much to relieve the pain except deep muscle massage.  Since it is 
allegedly a connective tissue problem, I don't see how CS would have much 
positive effect. She takes CS when she has a cold or flu, etc., but not 
regularly to try to deal with the fibromyalgia.   Anyone have experience 
getting relief using CS?
 
 So, since many of you have wide ranging experience with other cures, any 
suggestions on methods to reduce or cure the effects of fibromyalgia would be 
greatly appreciated.
 
 Thanks,
 --Steve 


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CSOTaerobic/anaerobic bacteria etc. and oxygen therpaies etc.OT

2000-07-11 Thread Ritz3131
Hi there,

I am wondering about oxygen therapies for aerobic and anaerobic bacteria as 
well as those somewhere in between.  If what I have read is accurate (and it 
may or may not be) the lyme bacteria borrelia bugrdoferi is microaerophilic 
which I think means it likes small amounts of oxygen (but I think not large 
amounts).  When I called labs etc. what I was told is that they think the 
Babesia which is a parasite and lives in the Red Blood Cells is aerobic.  The 
red blood cells is also where the borrelia burgdoferi lives and the red blood 
cells is where the oxygen is.  Now, I think it is assumed that aerobic 
bacteria and also partial anaerobes should be killed or at least knocked down 
by oxygen therapies but I am wanting to know what about the bacteria like 
lyme that are supposedly microaerophilic and live in the red blood cells and 
also aerobic organisms.  I wonder can oxygen therapies actually make any 
aerobic organism worse in int he worst case scenario would they just not do 
anything either way?

Thanks a lot,

Christy


In a message dated 7/10/00 10:09:49 AM Pacific Daylight Time, 
rogalt...@aol.com writes:

 
  
  mama2b...@aol.com wrote:
  
   Seratia
   I understand CS destroys the protein sheath surrounding anaerobic
   (harmful) bacteria and kills them but does not harm aerobic (friendly)
   bacteria.
   Somebody correct me if I'm wrong.
  
  Our tests have shown that CS kills both anaerobic as well as aerobic
  bacteria.  Actually this is good.  Many bacteria can switch from anaerobic
  to aerobic and back again instantly.  Also many aerobic bacteria can become
  pathogenic when misplaced.  For instance the bacteria essential in the gut
  can cause lots of problems if they colonize the vagina.  Although anaerobic
  = bad and aerobic = good has some basis in fact, it is not hard and fast. 


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CSLymemycoplasmaOT

2000-07-11 Thread Ritz3131
Hi Katiie,

I missed your original post so I don't have your email address here but I was 
positive for lyme as well as Mycoplasma fermentans (incognitus strain).  Do 
you know what strain or species of mycoplasma you have?  Let's keep in touch.


Christy

tIn a message dated 7/10/00 10:21:01 AM Pacific Daylight Time, 
kj...@erols.com writes:

 Katie Jay wrote:
 
   Hi all,
  
   I am going to start CS in a few days. I have Lyme and mycoplasma. How
 much
   CS should I take for active infections such as these? What quantity of
 what
   ppm? Does a person's weight factor in? A few swallows a day, as some
   recommend, is not enough specificity for me :o)
  
   Thanks,
   Katie 


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Re: CS[Fwd: continued]

2000-07-11 Thread Ritz3131
In a message dated 7/10/00 10:30:32 AM Pacific Daylight Time, 
rj...@dialnet.net writes:

  so important to them . Do you realize
 that one million children a year die of Malaria alone in Africa. Malaria
 is a tiny parasite that goes into your blood stream when stung. Both the
 CS and zapper destroy this tiny mite 
Hi Bob,

I have seen articles about the South African president.  He is saying he is 
not sure HIV causes AIDS and also that all the illness he sees in his country 
cannot be due to just one virus.  Well, I guess one of the organisms causing 
so much illness is the malaria organism.  I wonder what else besides or in 
addition to HIV he thinks may be contributing to AIDS.  Good luck with your 
work.  What dose of CS does it take to kill the malaria and what PPM and how 
long doe sit take.

God Bless,

Christy


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Re: CS overdose?

2000-07-11 Thread Ritz3131
Where did you get these quotes from?

Thanks,

Christy

n a message dated 7/10/00 11:37:30 AM Pacific Daylight Time, tw...@yahoo.com 
writes:

 
 Thanks,
 Hope
 krh...@worldnet.att.net
 
 Reply:
 
 Dr. John Barltrop of the University of Toronto
 conducted toxicity tests on rats, giving them enormous
 amounts of EGCS. He found there were absolutely no
 toxic effects. The amount he gave the rats (1 cc of a
 solution of 300,000 ppm of EGCS) was equivalent to
 7,500 times the amount other scientists found was the
 proper dose (10-40 ppm). The World Health Organization
 has stated, It is unnecessary to recommend any
 health-based guidelines for silver as it is not
 hazardous to human health.
 
 According to the U. S. Environmental Protection Agency
 (EPA) Poison Control Center, EGCS is considered
 harmless. Dr. Samuel Etris, a senior consultant at the
 Silver Institute, says there has never been any
 reports of allergenic, toxic or cancerous reactions to
 pure Colloidal Silver. The U.S. Government's Center
 for Diseases Control confirmed that fact in 1995. 


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Re: CSOT: Allergies

2000-07-09 Thread Ritz3131
Do you know how many grams of MSM you are taking a day?

Thanks,

Christy

In a message dated 7/7/00 9:43:40 AM Pacific Daylight Time, 
epmoon5...@aol.com writes:

 Subj: Re: CSOT: Allergies
 Date:  7/7/00 9:43:40 AM Pacific Daylight Time
 From:  epmoon5...@aol.com
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 HI. I have been able to stop taking Claritin prescription drug for about 3 
 months now. I have had severe allergy to sunshine, makes a itchie rash. Bug 
 bites that last and itch for a week. Have not been brave enough to try 
citrus 
 fruit, it puts me to bed with sneezing and a water spout for a nose. I have 
 been on MSM for 3 months. Am now taking about 3heaping teaspoons a day 
hoping 
 it will stop herniated disk pain in upper back. Its certinaly worth a try. 
 Very inexpenseive, though has a bitter taste. Betty Ft. Lauderdale   


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Re: CSThanks for the Lyme info

2000-07-09 Thread Ritz3131
In a message dated 7/7/00 1:57:39 PM Pacific Daylight Time, 
mayj...@javanet.com writes:

 I have been reading the government and health sites on the net.   
don't trust the government info.  Focus on other non-governement info.


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Re: CSLyme Disease

2000-07-09 Thread Ritz3131
In a message dated 7/7/00 5:53:38 PM Pacific Daylight Time, 
liah...@pacbell.net writes:

Hi Marsha,

Did you have TMJ?

Thanks,

Christy

 
 
 Dear Rob, Three days. I first noticed I could shut my jaw for the first time
 in months. The joints also eased up, and by a week, my mind was clearing and
 I could speak coherently!
 What a blessing CS has been!
 Marsha
 PS, Is it hot and muggy in Memphis? 


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Re: CS Effective Systematically

2000-07-07 Thread Ritz3131
In a message dated 7/5/00 2:03:51 PM Pacific Daylight Time, 
krh...@worldnet.att.net writes:

 Subj: CS Effective Systematically
 Date:  7/5/00 2:03:51 PM Pacific Daylight Time
 From:  krh...@worldnet.att.net
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Thanks to Roger for clarifying his statement about internal
 effectiveness. Thanks also to Marsha and James for posting their
 opinions that cs is effective when taken in this manner. I guess only
 time will tell as to how well it will work with my severe, long-term
 Lyme. I am taking about a quart to a quart and a half of homemade silver
 made with one of the CSPro Phasic systems.Hope
  
Hi Hope,

Are you still herxing or has that started to stabilize?

Good luck,

Christy


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Re: CSPoor Results when taken Systemically?

2000-07-04 Thread Ritz3131


Hi Hope and all,

Who is Dr. Altman?


Christy


krh...@worldnet.att.net writes:

 Subj: CSPoor Results when taken Systemically?
 Date:  7/4/00 4:35:49 PM Pacific Daylight Time
 From:  krh...@worldnet.att.net
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 On the other hand, I have noticed rather poor results with colloidal
 silver when it is used systemically. As a matter of fact, personal
 experience
 and that of others as well, has shown that CS does NOT compare well to
 antibiotics when used in this manner.
 
 As a relatively new member to this group, I was quite distressed by the
 above post by Dr. Altman. If the above is true, then why is it being
 touted by this list and cs manufacturers as being equivalent to
 antibiotics? I have long-term Lyme and in perusing the archives of this
 list and in speaking with several members here, I was fairly confident
 that I could use cs with good results.
 
 If that is not the case, then I obviously seriously need to rethink what
 I am currently doing.
 
 All feedback is appreciated. Since I get this list in digest form, posts
 cc'd to me as well as posted to the list, would be helpful. Thank you.
 
 Hope
 krh...@worldnet.att.net
  


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Re: CSlyme disease

2000-07-02 Thread Ritz3131
Hi Marsha, 

Curious where you read this.  I had a number of tick bites but I try to stay 
away from bugs in general now b/c you just never know.

Christy
a message dated 7/1/00 7:18:32 AM Pacific Daylight Time, liah...@pacbell.net 
writes:

 
 Dear Christy, and all,
 (Your spelling is right, but the species name has a small b!)
  I read recently that anything blood-sucking can now carry Bb. This includes
 mosquitoes and biting flies.
 Mine was definitely a deer tick, as I pulled the damn thing off my leg! Got
 the bullseye rash and the whole bit...sigh...
 Marsha
  


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Re: CSlyme disease

2000-06-30 Thread Ritz3131
In a message dated 6/29/00 3:37:28 PM Pacific Daylight Time, mo...@inow.com 
writes:

 Subj: CSlyme disease
 Date:  6/29/00 3:37:28 PM Pacific Daylight Time
 From:  mo...@inow.com (Mary)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 What causes lyme disease? Is it caused by a vax? I know the story about the
 ticks but I'm just wondering if there is another story we don't hear about. 

I think with many things we only hear part of the story.  It certainly would 
not suprise me to find out that there may be additional modes of transmission 
besides tick.  Lyme is caused by a bacteria called Borrelia 
Burgdorferi...spelling may be off.

Christy


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CSOT oxygen therpaies

2000-06-27 Thread Ritz3131
 
---BeginMessage---
Hi all,

I am wondering if anyone can tell me if oxygen therapies should help knock 
down or eradicate the lyme bacteria borrelia burgdorferi, and/or Babesia, 
and/or ehrlichia?

Thanks a lot,

Christy
---End Message---


Re: CSOT whoa - got to jump in here - Christy

2000-06-23 Thread Ritz3131
IThanks.  Will avoid all the time.  Only have a diet coke about once a month 
like if at the movies but won't anymore.

Christy

n a message dated 6/22/00 4:37:12 AM Pacific Daylight Time, li...@flash.net 
writes:

  Christy, List, et al:
  
  YOUR shakiness is being caused by the aspartame in diet coke AND it also
  actually makes you hungrier and makes your hypoglycemia worse and of course
  eventually brain tumors . .  yep (that is the end result of formalydehyde).
  
  Jeannine 


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Re: CSCMO-bloodsugar-lowOT

2000-06-21 Thread Ritz3131
In a message dated 6/21/00 5:39:44 AM Pacific Daylight Time, 
galing...@chariot.net.au writes:

 Subj: Re: CSCMO-bloodsugar-lowOT
 Date:  6/21/00 5:39:44 AM Pacific Daylight Time
 From:  galing...@chariot.net.au (Judith Thamm)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 As you are a diabetic are you using an artificial sweetener in
 anything?  One of the side effects of some artificial sweeteners is
 that they send blood sugar out of kilter and cause the weak/shaky 
 feelings you have described.  [Aspartame, NutraSweet, Equal and all
 the other names it goes under.]
 Judith. 
Hi.  I am not diabetic.  I have low blood sugar.  I avoid that stuff about 
95% of the time.  Have noticed getting shaky after diet coke which I very 
rarely have but I thought it was the caffeine...maybe not...or both.  What 
about saccharin...worse or better than nutrasweet and/or sugar?

Christy


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Re: CSCMODosageOT

2000-06-21 Thread Ritz3131
In a message dated 6/21/00 1:58:27 PM Pacific Daylight Time, 
pjgr...@northnet.org writes:

 Subj: Re: CSCMODosageOT
 Date:  6/21/00 1:58:27 PM Pacific Daylight Time
 From:  pjgr...@northnet.org (Pamela Grant)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 The below is interesting as I too had the mycoplasma type of
 pneumoniaApril'99) and have recently been quite shaky also. Is shakiness
 and that particular illness have a correlation---anyone know?
 
 Pam 
Hi Pam,

Check out www.immed.org.  I had a severe case of Mycoplasma pneumonia 
diagnosed through chest x-rays, fact that I was coughing up blood, etc. and 
blood work was done but I am sure they did not do a PCR to determine what 
strain of mycoplasma.  Most labs do not.  I later was positive on PCR and 
Gene Tracking when tested for M. fermentnas incognitus which can cuse many 
chronic and serious symptoms.  When monkeys were injected with it they died 
in 7 to 9 months according to Dr. Lo who has the patent on it.

Christy


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Re: CSOTMarsha-lymelists,cyst form of lyme

2000-06-21 Thread Ritz3131
In a message dated 6/21/00 3:31:45 PM Pacific Daylight Time, 
pjgr...@northnet.org writes:

 Subj: Re: CSOTMarsha-lymelists,cyst form of lyme
 Date:  6/21/00 3:31:45 PM Pacific Daylight Time
 From:  pjgr...@northnet.org (Pamela Grant)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 What is the magnetic pulser?
 
 PG 
see www.sota-inc.com


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CSCMO-bloodsugar-lowOT

2000-06-20 Thread Ritz3131
Hi all,

I am wondering if CMO can cause problems for people with low blood sugar if 
anyone knows.  I have been taking it (of course I am doing a lot of other 
things including cs etc. but I would not think cs could cause problems with 
that) and I am noticing that my symptoms of low blood sugar (shakiness) are 
worse even though I am making special efforts to eat well and not wait too 
long in between eating but it seems I am having to eat more and more often 
than normal lately to avoid becoming shaky.  I do have low blood sugar but 
normally am ok if I make sure I eat often enough and make sure I get enough 
protein as well.

I really don't know what to think b/c this weak/shaky feeling can also go 
along with herxing or die off from various things and that could be part of 
it but it does seem my blood sugar problems are worse than normal.  For 
example, yesterday I ate good meals but was still weak/shaky all day until I 
finally ate a who;e bunch of different stuff..one after the other late in the 
evening/night...then felt not shaky finally.  I took my CMO before bed and 
woke up shaky a few hours later when i I got up to go to the bathroom and 
when I woke up a number of hours after that I was quite shaky and still am.

I do know in my Prescription For Nutritional Healing Book that it says people 
with diabetes shouldn't take fish oil b/c of the high fat content but I have 
never had a problem with taking fish oil which I am still taking as well as 
flax oil.  Plus, I do not have diabetes...just low blood sugar and a 
chiropractor thought hyperinsulinemia or something like that what ever that 
means.  He just said make sure to get lots of protein.

I have been having night sweats which does seem to be for me a die off/herx 
symptom with various things including for example, when starting each new 
antibiotic for Mycoplasma fermentans incognitus.  When I started Biaxin in 
addition to the night sweats I felt shaky weak for a number of weeks and then 
it died off and I also was eating more and the first couple nights woke up so 
shaky I had to scarf down a bunch of food.  But, still this doesn't seem good 
to me.  I also recently have been making sure to take digestive enzymes with 
the CMO (as I have heard recommended) to make sure it is absorbed and have 
been noticing more night sweats.  Supposedly studies have shown the CMO has 
prevented arthritis in rats injected with Mycobacterium butyricum (also known 
as Freund's adjuvant) while the other rats injected with the organism but 
that did not get any CMO experienced major symtpoms of arthritic 
disease.(Journal Of Pharmaceutical Sciences, Vol. 83 (3) March 1994 
296-299)...this came from a booklet I got a the health food store..have not 
seen actual study from journal.

I am wondering if maybe I should decrease my dose of CMO.

Christy


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CSCMODosageOT

2000-06-20 Thread Ritz3131
Hi all,

Wondering if anyone can help me with CMO dosage.  A booklet I have from the 
health food store says typical amounts range from 0.05 to 0.75 grams of CMO 
per 140 to 200 grams of body weight.  Well, I weigh about 105 now if my scale 
is accurate just checked.   (I'm a shrimpy...smile...about 5 feet 
1/2inches.)  I tried figuring out the math but my numbers don't seem to be 
making any sense at all.  Someone told me there are 453.6 grams in a pound.  
Anyone know if that is correct?

I have been taking 2 500mg capsules (1000mg) 3 times a day.  It says on the 
label a 1000mg dose provides 200mg Cetyl Myristoleate and other mixed fatty 
esters.)  Anyone have any input on what the right dose for me is?

Thanks,

Christy


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CSFwd: CMO-bloodsugar-lowOT

2000-06-20 Thread Ritz3131
CMO is a fatty acid ester.  It isa lipid-based compound composed of Omega-3 
fatty acids.  (Omega 3 fatty acids are found is some cold water fish.  The 
booklet I got from the health food store says, the fact that it is found in 
sperm whale oil suggests that it may have significant therapeutic effects for 
joint inflammations.  The booklet also says Swiss albino mice naturally have 
CMO and do not get arthritis when injected with Freund's adjuvant which is 
Mycobacterium butyricum.  This booklet is by Woodland Health Series and is 
called CMO Cetyl Myristoleate A Natural Treatment For Arthritis and Other 
Joint-Related Diseases by Rita Elkins, M.H.

Christy
---BeginMessage---
Hi all,

I am wondering if CMO can cause problems for people with low blood sugar if 
anyone knows.  I have been taking it (of course I am doing a lot of other 
things including cs etc. but I would not think cs could cause problems with 
that) and I am noticing that my symptoms of low blood sugar (shakiness) are 
worse even though I am making special efforts to eat well and not wait too 
long in between eating but it seems I am having to eat more and more often 
than normal lately to avoid becoming shaky.  I do have low blood sugar but 
normally am ok if I make sure I eat often enough and make sure I get enough 
protein as well.

I really don't know what to think b/c this weak/shaky feeling can also go 
along with herxing or die off from various things and that could be part of 
it but it does seem my blood sugar problems are worse than normal.  For 
example, yesterday I ate good meals but was still weak/shaky all day until I 
finally ate a who;e bunch of different stuff..one after the other late in the 
evening/night...then felt not shaky finally.  I took my CMO before bed and 
woke up shaky a few hours later when i I got up to go to the bathroom and 
when I woke up a number of hours after that I was quite shaky and still am.

I do know in my Prescription For Nutritional Healing Book that it says people 
with diabetes shouldn't take fish oil b/c of the high fat content but I have 
never had a problem with taking fish oil which I am still taking as well as 
flax oil.  Plus, I do not have diabetes...just low blood sugar and a 
chiropractor thought hyperinsulinemia or something like that what ever that 
means.  He just said make sure to get lots of protein.

I have been having night sweats which does seem to be for me a die off/herx 
symptom with various things including for example, when starting each new 
antibiotic for Mycoplasma fermentans incognitus.  When I started Biaxin in 
addition to the night sweats I felt shaky weak for a number of weeks and then 
it died off and I also was eating more and the first couple nights woke up so 
shaky I had to scarf down a bunch of food.  But, still this doesn't seem good 
to me.  I also recently have been making sure to take digestive enzymes with 
the CMO (as I have heard recommended) to make sure it is absorbed and have 
been noticing more night sweats.  Supposedly studies have shown the CMO has 
prevented arthritis in rats injected with Mycobacterium butyricum (also known 
as Freund's adjuvant) while the other rats injected with the organism but 
that did not get any CMO experienced major symtpoms of arthritic 
disease.(Journal Of Pharmaceutical Sciences, Vol. 83 (3) March 1994 
296-299)...this came from a booklet I got a the health food store..have not 
seen actual study from journal.

I am wondering if maybe I should decrease my dose of CMO.

Christy

---End Message---


cselectroporation/lyme,M.incognitus

2000-06-20 Thread Ritz3131
Now, would the electroporation be good when using CS for lyme and/or for 
Mycoplasma fermentans inocgnitus which the M. incognitus burrows deep into 
the cells and I beleive the lyme does also to help the CS get into the cells 
better???

Christy


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CScyst lyme/babesia,erlichiosis

2000-06-20 Thread Ritz3131
So, have you tried those drugs again or just sticking with CS?  Also, know 
much about babsesia and erlichiosis?  Do you know if Cs should work for those 
also?

Thanks,

Christy

 a message dated 6/20/00 2:51:19 PM Pacific Daylight Time, myf...@mwt.net 
writes:

 Subj: Re: CSOTMarsha-lymelists,cyst form of lyme
 Date:  6/20/00 2:51:19 PM Pacific Daylight Time
 From:  myf...@mwt.net (Scharbach)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 There has been some study done on using Flagyl for this reason.
 
 It kills the cyst form, but has no effect on the spirochetal stage.
 It (Flagyl) must be used in combo with Zithromax or tetracyclin,or
 doxycyclin.
 
 Supposedly three months of this combo will take care of the LYme.
 I tried it.   I was well into my 6th week when my heart went nuts.
 Ended me in ICU.
 
 Found out later, this is an extreme herx reaction and will eventually
 pass, as the Lyme dies off.   Yipes!!
 
 Sparrow
  


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Re: CSCMODosageOT

2000-06-20 Thread Ritz3131
I've been taking CMO about 3 weeks.  I have been doing lots of things but 
adding the CMO is the most recent.  Ever since I got a bad case of mycoplasma 
pneumonia over 9 years ago I get shaky if I have not eaten for a while but it 
has been worse lately...for about 2 weeks I'd say.

Christy

In a message dated 6/20/00 3:29:00 PM Pacific Daylight Time, li...@flash.net 
writes:

   Re: CSCMODosageOT
 Date:  6/20/00 3:29:00 PM Pacific Daylight Time
 From:  li...@flash.net (d.linen)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Christy,
 
 How long have you been taking the CMO? Were you shaky before you ever
 took any CMO? It sounds like you are taking a variety of different
 things. So you only got shake when you introduced the CMO into your
 regimin? 
 
 Diane 


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Re: CSCS and Lyme

2000-06-19 Thread Ritz3131
Hi Marshall,

I was wondering if your sister stopped all herbs, vitamins and other 
supplements while using the Sota units due to electroporation issues or if 
she kept taking supplements?  Some say it is OK to take supplements after 
using the units I think but not to take them before.

Have you heard of the units by Michael Forrester?  A woman on another list 
says his units have the option of using 100hz which does not cause 
electroporation.  Do you know anything about that?

Thanks,

Christy


Thanks,

Christyn a message dated 6/19/00 8:10:48 AM Pacific Daylight Time, 
mdud...@execonn.com writes:

 Subj: Re: CSCS and Lyme
 Date:  6/19/00 8:10:48 AM Pacific Daylight Time
 From:  mdud...@execonn.com (Marshall Dudley)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 I belive that you will find that CS alone will not be able to get to all the
 Lyme bacteria, they are really good at hiding in the brain, lymph system and
 cartlidge after you have had it long term.
 
 I would suggest using the full 4 step protocol of Bob Beck's for a rapid and
 complete recovery.
 
 His protocol uses CS, ozonated water, blood electrification (I use Clark's
 zapper though), and magnetic zapping. CS alone helped my sister get to about 
80%
 from her Lyme, but it took all four for a complete cure.
 
 See http://rarebooks.net/beck.html and http://www.sota-inc.com
 
 Marshall 


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CSCMO OT

2000-06-19 Thread Ritz3131
Hi.  I was wondering if CMO is ever taken long term or if it is only taken 
for about 30 days to 6 weeks?  Also, does anyone know if it is dangerous to 
take long term?  I am wondering what the mechanism of action is.  I have 
heard and read different theories/possiblilities.  These induce that the CMO 
took away arthritis that had been induced in rats in an experiment by 
injecting them with a mycobacterium?  Are others aware of this?  Could the 
CMO have antibiotic properties?

Thanks,

Christy


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CSMarsha ppm lyme,mycoplasma fermentnas incognitus

2000-06-19 Thread Ritz3131
Hi Marsha (and all),

I have been meaning to email you...don't have your address handy though.  
But, I think you said you use 18ppm for the lyme?  Do you have an instrument 
that measures the ppm?  Where does one find those?  Does you cs look kind of 
gold?  If you want an 18 ppm as opposed to say 5 ppm do you need to have the 
cs cooking for a few more minutes?  I think I have been making about 5ppm 
and it looks clear but when I let it cook about an extra 5 minutes (in 
addition to the normal 15 I do which I think makes about 5ppm) it then has a 
definite goldish cast to it...at that point do you think it is closer to 18 
ppm?  I have been thinking maybe I should do 5ppm once a day and then take 18 
ppm another time during the day to get both in case one is better etc.   I 
heard 5ppm is good for the Mycoplasma fermentans incognitus which I was 
positive for.  But, I am also positive for lyme.

Well, I feel like I am forgetting something but obviously can't remember 
what.  Oh...I know...is it OK to make and store or best to make and use right 
away?  Do you make just enough to use or do you end up having to throw some 
away?

Thanks,

Christy


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Re: CSCS and Lyme

2000-06-19 Thread Ritz3131
Hi again,

Thanks for your reply.  Can you or anyone else tell me what is supposed to be 
so bad about garlic?  Everything I have read about it is very good.

Thanks,

Christy

In a message dated 6/19/00 5:14:48 PM Pacific Daylight Time, 
mdud...@execonn.com writes:

 She used the Sota ozonator and pulsar, but used my CS and Hulda Clark's 
zapper.
 She only avoided garlic as far as I know.
 
  


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CSOTMarsha-lymelists,cyst form of lyme

2000-06-19 Thread Ritz3131
Hi Marsha and all,

A couple more questions...smile.  I think you said in the past you are on 
both Lyme-aid and also sci.med (or something like that...another lyme list).  
I have noticed that on the Lyme-aid list their is a lyme doctor named Lynn 
who posts a lot.  Is she also on the sci.med list?  Also, can you tell me if 
you get as many posts on the sci.med list and also if they discuss many 
alternative treamtnets for lyme on that list or not and if the list is pretty 
treatment focused?  Also, wondering if you can tell me what the cyst form of 
lyme means?


Thanks a lot.  I appreciate all your help and input as well as everyone's on 
this list.

Christy


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Re: CSNew to List

2000-06-07 Thread Ritz3131
Hi Jeannie,

Keep in touch with me.  Did you know evening primrose can increase estrogen?  
Some women may not want to do that.I  Also, did you say you were on Lyme-AID? 
An MD seems to think some MS cases may be Lyme.  Also, I am also rifing.  I 
can tell you more later if you want.  I have had MS symptoms and their is 
even a family history of it but they seem to be getting better.  I a recently 
started doing freqs on the rife machine for lyme in addition to the other 
ones i was doing.

Christy

 a message dated 6/5/00 9:37:55 PM Pacific Daylight Time, 
jean...@karlster.com writes:

 Subj: RE: CSNew to List
 Date:  6/5/00 9:37:55 PM Pacific Daylight Time
 From:  jean...@karlster.com (Jeannie)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Hi Christy...
 I was using only 10ppm two times per day.  It took about 2 months for me to
 start really feeling its affects.  Although I was also taking a number of
 other supplements, some of which I have returned to, such as pantothenic
 acid (up to 1500 mg/day), CoQ10, primrose oil, calcium/magnesium supplement,
 garlic tablets, B-complex, flax seed, and fish oils.
 
 A nurse practitioner who knows about these problems also believes that it's
 probably CNS Lyme.  The only thing is that when this 'episode' started
 similar symptoms began, but showed themselves in slightly different ways.
 Because of my long term experience with this, it completely threw me.  I
 will have to wait and see.  But I certainly won't sit back and wait.
 
 Thanks for the message.
 
 Jeannie
  


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Re: CSNew to List

2000-06-05 Thread Ritz3131
Hi Jeannie,

I would assume its probably CNS Lyme.  That's great the success you had with 
CS in the past.  I would go back to that and stay on it.

Can I ask what ppm you used and what dose?

Thanks,

Christy

In a message dated 6/5/00 4:30:47 AM Pacific Daylight Time, 
ar...@nf.sympatico.ca writes:

 
  Hi to all... I just subscribed to this list because I found
  colloidal silver (again).  A few years ago I was diagnosed with
  Lyme Disease, after spending 3 years being misdiagnosed and
  almost crippled.  After finally receiving antibiotic therapy
  and my body not tolerating such after a couple of years, I
  turned to alternative medicine.  Several homeopaths and
  nutritionists had told me about colloidal silver, so I began to
  do my own investigation on the limited literature available at
  the time.
 
  I found that it really helped me alot and after about a year, I
  fell off the wagon (so to speak) because I was feeling pretty
  good.  About 8 months ago, I started slipping again into a
  stupor, double vision, trouble with speech and gait and once
  again started on the travails to find out what was wrong.
 
  It again is a question mark between MS and CNS Lyme Disease.. I
  guess my question right now is, if it is MS, will taking the
  Colloidal Silver hurt me in any way.  Does anyone know anything
  about this?
 
  Thank you and good health to all of you,
 
  Jeannie 


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Re: CSlyme-aid list

2000-06-04 Thread Ritz3131
Hi Mary,

Please let us know which list you think is better in terms of 
infotreatment info

 I also just signed up on Lyme-Aid.  I would sign up on both but I can barley 
handle all the lists I am on now.  If you have a chance and its not too much 
trouble could you ask on the sci.med one if they know of any lyme literate 
docs in St. Louis, MO or nearby?  Recently, I got postiive lyme tests.

thanks,

Christy

n a message dated 6/4/00 2:26:55 PM Pacific Daylight Time, helenw8...@aol.com 
writes:

 Subj: CSlyme-aid list
 Date:  6/4/00 2:26:55 PM Pacific Daylight Time
 From:  helenw8...@aol.com
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Marsha, I belong to the lyme-aid list that has over 200 members and about 20 
 messages a day   lyme-...@egroups  they post about CS also. Just signed up 
 for sci.med.diseases.lyme. 
 
 Thanks,   Mary 


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CSOT lymeliteratedocSt.Louis?Disabilityetc.

2000-06-04 Thread Ritz3131
Hi to the lyme people.  I am forwarding this email to fill you in on my 
situation.Some forms of mycoplamsa do not cause serious problems but 
Mycoplasma fermentans (incognitus strain) is the strain that Dr. Lo of the 
Armed Forces has the United States patent on which states when it was 
injected into monkeys they died in 7 to 9 months.  It is being found in 1/2 
of the sick Gulf War vets and a smaller percentage I believe of CFS and Fibro 
people.  It can cause many of the same symptoms as lyme.  That's why I 
thought the odds were against me having both.  It is air borne according to 
Dr. Garth Nicolson (www.immed.org) and also spread through saliva, sex, and I 
believe sweat.  Is the lyme contagious also and if so how is it transmitted?

Also, is headaches on the top of the head espeically in warm environments 
known to be a symptom of lyme?

Also, I am doing my own alternative therapy but I guess it may be good for me 
to have a doc who is lyme literate if there are any in my area.  Do you know 
of any in St. Louis, MO or nearby?

Also, is it hard for lyme people to get disability?

Thanks,

Christy
---BeginMessage---
 
---BeginMessage---
Hi guys!  Yes, I do think the dna helper is on to something and   I do 
appreciate all the work the DNA helper is doing.  I was going over an email 
post to the list from the helper from about March with some numbers for 
Borrelia Burgdorfi (it's down stairs) the other day and noticed that a bunch 
of the numbers (or very close numbers) are also listed on the Dan Tracy/Jim 
Bare list I printed off of Turf's site and/or on a list that Don Tunney's 
assistant sent me of freqs used for Lyme that they found some of their CFS 
volunteers where having hits with.  Anyway, I found that quite 
interesting...smile!!!  Also, I have been having hits with those numbers from 
the email that I have done...mostly strong tostrong underlined.

A couple weeks ago I took a week (or 6 days) off of all supplements and 
rifing (I felt worse during that time...starting a few days after stopping 
the stuff).  Anyway, I then had my blood shipped to Dr. Lidda Mattmann 
(spelling??) in  Michigan and a lab in Floridia...Bowen Research and Training 
Institute and I got all my results in now.  They both tested for Borrelia 
Borgdorfi and said I was positive.  Mattman does a blood culture from your 
blood and sends pictures of the spirochetes.  The other lab did rapid 
fluorescent antibody technique for Borrelia.  Bowen also said peripheral 
blood smear suggests:
Human Granulocytic Erhlichia (HGE) and Babesia...confirmation of indicated.  
Well, I am sick of paying for and getting blood drawn and sent to labs etc. 
so i will just assume I may have those so if you have any freqs for those let 
me know.  I really don't know a whole lot about these labs or tests but a few 
weeks  or so ago I started wondering if I could have lyme in addition to the 
Mycoplasma fermentans incognitus.  In the past I have talked to like Dan 
tracy for instance and he went through like a list of 30 symptoms with me 
asking me if I had them and I kept saying yes, yes, yes, etc. and he kept 
saying you have Lyme and I kept saying but you don't understand I have 
Mycoplasma fermentans incognitus and it can cause about all the same symtpoms 
and the whole illness started with a bad case of mycoplasma pneumonia so it 
makes sense that since I developed chronic symptoms the whole thing was 
caused by the Mycoplasma fermentans incognitus which can cause systemic and 
chronic illness.  He just kept saying I had Lyme but it never occured to me I 
could be unlucky enough to have both.  But, one thing I do remember is ever 
since like around maybe 5th or 6th grade or so I would get real bad headaches 
if out in the sun and heat for hours.  And, this lady said she thought that 
could be from the lyme.  Anyway I prayed to God to send me a sign or help me 
know if I had lyme.  Well, the next day or so I had a dream in which I was at 
like a dance and I was wearing a bright lyme green real fancy dress and so 
was another lady in the dream.  Then when I woke up I thought boy was that 
weird nobody wears that color...that lyme green, anymore...how weird...nobody 
has worn anything like that for years since like the 80's.  But, at the time 
that's all I thought about it...didn't get the lyme as in borrelia yet at 
that point.  Then that night my dad was watching Lawrence Welk and I was 
watching it...ugghh!!...LOL!!! while eating dinner and out comes this woman 
in a real fancy dress that was bright lyme green.  Then comes out another 
woman in a another fancy lyme green dresssame color but different style 
(as in my dream) and then I think the  third lady came out like that also but 
again different style...same color.  And, I thought boy that's weird and 
mentioned my dream to my dad.  And, ht Lawrence Welk show looked like it was 
made in like the 80's (early I guess) by the hair styles/feathered hair, etc. 
and of course the 

CSPPM, Lyme

2000-06-04 Thread Ritz3131
Hi all.  2 questions.  One very basic...what does parts per million actually 
mean?  And, for example, is 18 ppm smaller or larger particles of silver than 
5 for example?  Also, what do you think of 5 ppm for lyme?

Thanks,

Christy


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Re: CS, Lyme List versus Marsha

2000-06-03 Thread Ritz3131


Hi Marsha,
What lyme list(s) are you on?  which do you find to be the most helpful in 
terms of info. and treatment info.?  I forget, what ppm did you use...was it 
10ppm?  Do you still use it?

Also, you or anyone know any lyme literate docs in the St. Louis, MO area?

Thanks,

Christy

In a message dated 6/3/00 9:12:58 PM Pacific Daylight Time, 
liah...@pacbell.net writes:

 I really think CS can do the trick if done properly.
 Marsha
 (by the way, there`s no need to shout...)
 
  


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Re: CSBursitisCMO

2000-05-31 Thread Ritz3131
In a message dated 5/30/00 8:25:52 AM Pacific Daylight Time, Hi Marshall,

Thanks for the info. on the previous posting about your sister, etc.  Just 
wondering do you know anyone who has used CMO for Lyme or other bacterial 
things or rheumatoid arthritis and what results they had?  Is it true you 
only need to take it for 30 days?

Thanks,

Christy

mdud...@execonn.com writes:

 Subj: Re: CSBursitis
 Date:  5/30/00 8:25:52 AM Pacific Daylight Time
 From:  mdud...@execonn.com (Marshall Dudley)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Try CMO.
 
 Marshall
 
 frineha...@aol.com wrote:
 
  Beginning about 3 weeks ago I experience soreness and at times excruciating
  pain,
  depending on extent of arm movement, in my left shoulder.  Initially I
  thought I was having a bout with arthritis (I'm 62), but after doing some
  research I have concluded that I have bursitis.   I take 4-6oz. CS each 
day.
   Anyone have suggestions for treatment?
 
  Thanks,
 
  Frank in South Texas 


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Re: CSDr Clark on CS

2000-05-31 Thread Ritz3131
Is this Dr. Hulda Clark?  I can't get the web site.

thanks,

Christy

n a message dated 5/31/00 2:33:26 PM Pacific Daylight Time, 
apothec...@home.com writes:

 Subj: Re: CSDr Clark on CS
 Date:  5/31/00 2:33:26 PM Pacific Daylight Time
 From:  apothec...@home.com (James Allison)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
  http://www.drclark.ch/bulletin/cs.htm
 
 The following are a couple of quotes from the above site, and then a
 question:
 
 What exactly is Colloidal Silver (CS)? Simply put, colloids are extremely
 minute-sized silver particles suspended in water, with a positive electrical
 charge. The smaller the silver particles, the more effective it has proven
 to be. The best Colloidal Silver is produced at the molecular level. A small
 DC current is passed through an electrolyte with silver electrodes. Minute,
 molecular sized particles are drawn off the positive electrode, having a
 positive electrical charge. This electrical charge is of primary importance
 to healing and antibacterial qualities. The charge slowly dissipates, and
 therefore the freshness of the colloid is important.
 
 When current is applied to silver in solution the particles that break off
 will always be the same size: 1.26 angstroms (.000126 microns).
 
 Now, once again, can somebody please tell me how AC units make a better
 solution than LVDC units?
 
 Yours in health,
 James Allison
  


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CSBeck's tools/cs dosing times per day.away from food??etc.

2000-05-26 Thread Ritz3131
Hi Marshal,

How long was your sister sick before she started the cs and then the 4 part 
protocol?  Was she using the Sota device to make the CS.  Do you know what 
ppm she was using and waht dose of CS?  Also, is it best to take CS twice a 
dfay or once or even 3 times?  Should it be taken on an empty stomach or a 
full one or does it matter?  Also, will supplements or herbs interfer with 
it..should thety be spaced apart?

Thanks,

Christy

n a message dated 5/26/00 8:09:33 AM Pacific Daylight Time, 
mdud...@execonn.com writes:

 Subj: Re: CSBob Beck's super tools
 Date:  5/26/00 8:09:33 AM Pacific Daylight Time
 From:  mdud...@execonn.com (Marshall Dudley)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Alvin Rose wrote:
 
  I notice a number of people on the Silver List have contacted
  lyme disease..I am curious as to if anyone has tried the Beck
  devices
  to cure this Problem..I use them often and have had great success
  with them
  Both the blood electrifier and magnetic pulser combined with
  Colloidal Silver
  should cure most problems..I don't have lyme disease but I feel
  that these
  devices should do the job if the 4 step protocol is used as
  required.
  A.Rose
 
 Yes.  As I have reported to this list several times, my sister was able to
 improve tremendously on CS, but could not complete get rid of it. She was
 unable to get it out of her joints and lymph system. The use of all 4 of the
 Beck protocols and she was free of all symptoms in a month and her lymph
 nodes went down for the first time in years.
  


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Re: CSMSM herx/detox

2000-05-25 Thread Ritz3131
MSM can cause those symptoms when you start taking it.  It detoxes you...gets 
toxins out and you feel those symptoms as it does that.  Also, it is sulfu 
and when I looke dthat up in my Perscription for Nutritional Healing it says 
sulfur is antibacterial and antiviral so you also may be experiencing 
herxing/die off of viruses and/or bacteria.

You can reduce the dose for a while and this should decrease.  Keep drinking 
lots of water.  I would take this as a good sign that its working.

Christy

n a message dated 5/25/00 5:07:29 AM Pacific Daylight Time, mzo...@aol.com 
writes:

 Subj: CSMSM
 Date:  5/25/00 5:07:29 AM Pacific Daylight Time
 From:  mzo...@aol.com
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Hello everyone,
 I just looked in the archives trying to locate something about the 
 possible detrimental effects of MSM. I found a few tidbits there, but not 
 what I was looking for, so I'll pose some questions here.
 Does anyone have an idea as why when upon taking MSM for the first time 
 last night, it made me sick. I think I am allergic to it. 
 Why would one be allergic to a natural substance from the earth? 
 I know it was the MSM that made me sick, for within an hour or so of 
 taking it, I began getting a feverish achy feeling all over. I went to bed 
 early, tossed and turned all night (my husband said I was even moaning when 
I 
 was asleep). I felt as if I had the flu. This morning I am feeling better 
 after LOTS of water to flush it out of my system.
 Many years ago, enough so that I had totally forgotten (until last 
night) 
 I had some sulfur prescribed for something or other. I had a reaction to it 
 then too...feverish flu like symtoms.
 Any thoughts? Thanks.
 Love, Kathy 


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Re: CSMSM

2000-05-25 Thread Ritz3131
What brand is the brand that makes your wife sick?

Thanks,

Christy

In a message dated 5/25/00 7:12:51 AM Pacific Daylight Time, 
mdud...@execonn.com writes:

 Subj: Re: CSMSM
 Date:  5/25/00 7:12:51 AM Pacific Daylight Time
 From:  mdud...@execonn.com (Marshall Dudley)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 mzo...@aol.com wrote:
 
  Hello everyone,
  I just looked in the archives trying to locate something about the
  possible detrimental effects of MSM. I found a few tidbits there, but not
  what I was looking for, so I'll pose some questions here.
  Does anyone have an idea as why when upon taking MSM for the first time
  last night, it made me sick. I think I am allergic to it.
 
 You may have some with some impurities in it.  We have bought 4 different 
brands
 of MSM and one of them makes my wife sick.  They are all suppose to be pure, 
but
 I suspect that one has some leftover solvents in it or something.
 
 
  Why would one be allergic to a natural substance from the earth?
  I know it was the MSM that made me sick, for within an hour or so of
  taking it, I began getting a feverish achy feeling all over. I went to bed
  early, tossed and turned all night (my husband said I was even moaning 
when I
  was asleep). I felt as if I had the flu. This morning I am feeling better
  after LOTS of water to flush it out of my system.
 
 Those are exactly the same symptoms my wife gets on that particular brand.
 
 
  Many years ago, enough so that I had totally forgotten (until last 
night)
  I had some sulfur prescribed for something or other. I had a reaction to it
  then too...feverish flu like symtoms.
 
 
 You are likely referring to a sulfa drug.  Entirely different animal.
 
 Marshall 


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Re: CSPotato extract: A new direction for antibiotics

2000-05-25 Thread Ritz3131
I would like to know this also.

Thanks,

Christy

In a message dated 5/25/00 2:59:53 PM Pacific Daylight Time, 
brownin...@hotmail.com writes:

 Subj: RE: CSPotato extract: A new direction for antibiotics
 Date:  5/25/00 2:59:53 PM Pacific Daylight Time
 From:  brownin...@hotmail.com (rob gr)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Hey James, i would really like to know the answer to that one too.
 
 If I am going to use Silver properly to treat my Lyme- the right dosage 
 concentration seems to have some correlation.
 
 Just curious - have there been research on what concentration of CS is 
 required to inhibit/kill Lyme? Also how does that translate into the ppm and 
 dosage that should be taken?
 
 rob
 in memphis 


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Re: CSInfantile asthma -- Will CS help?

2000-05-19 Thread Ritz3131
In a message dated 5/19/00 12:15:31 PM Pacific Daylight Time, 
liah...@pacbell.net writes:

 Subj: Re: CSInfantile asthma -- Will CS help?
 Date:  5/19/00 12:15:31 PM Pacific Daylight Time
 From:  liah...@pacbell.net (Marsha Hallett)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Dear Christy, All I can say is since I began taking CS 4 years ago, I have
 had no more asthma, and only tiny effects of hay fever, a few sneezes and
 itchy eyes, which a fresh dose of CS stops.
 In my opinion, CS will help her!!
 Marsha 
Hi Marsha

Just wondering are you still on cs daily and have you taken it for 4 years 
straight every day?

Thanks,

Christy...a different Christy


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Re: CSSilver - an article

2000-05-12 Thread Ritz3131
I was not able to access that article.  I someone could post it that would be 
appreciated.

Thanks,
Christy

In a message dated 5/12/00 2:47:38 AM Pacific Daylight Time, i...@win.co.nz 
writes:

 Subj: Re: CSSilver - an article
 Date:  5/12/00 2:47:38 AM Pacific Daylight Time
 From:  i...@win.co.nz (Ivan Anderson)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Dear Jeanne,
 
 That is good news!
 UTI, arthritic inflammation, dry eyes, cold infection, and morning
 breath, banished over night... wow! No wonder you're chuffed.
 
 (My Uncle swears he can bowl all day long now that he takes CS, whereas
 his legs couldn't go past a couple of hours beforehand.)
 
 No Herxheimer reaction or die-off either.
 
 BTW did you happen to read the article ;-)
 
 Regards
 Ivan. 


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Re: CSSilver - an article

2000-05-12 Thread Ritz3131
Hi Marsha and all,

I have wondered weather silver is considered a heavy metal or not.  Like for 
instance, I believe aluminum and mercury are considered heavy metals which 
are thought to be able to cause health problems when they build up in the 
body.  What is different about silver?  Excuse my ignorance but I just don't 
know the intricacies of these things.

Christy

In a message dated 5/12/00 8:34:05 AM Pacific Daylight Time, 
liah...@pacbell.net writes:

 Subj: Re: CSSilver - an article
 Date:  5/12/00 8:34:05 AM Pacific Daylight Time
 From:  liah...@pacbell.net (Marsha Hallett)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 
 
  This is a very interesting read.
 
  http://www.silverinstitute.org/news/bkhealthmet.html
 
  Ivan.
 
 Dear Ivan, Yeah, but this part bugs me:
 The removal of silver and other heavy metals is the function of the
 metallothioneins. These ubiquitous proteins are found in all vertebrates and
 invertebrates and act to transport, store, and detoxify essential and
 nonessential trace metals. The metallothioneins chelate or agglomerate heavy
 metals and convey them from the body. Their action can be overwhelmed by
 ingestion of excessive amounts of heavy metals. In the case of silver,
 excessive amounts may eventually deposit in the skin, giving it a gray
 color. This deposit is called argyria and cannot be removed.
 
 Silver, being a highly conductive metal, has been shown to have a
 deleterious effect in the presence of nerve cells. While heavy metals are
 blocked from the nervous system and the brain by the blood-brain barrier by
 a membrane whose purpose is to filter out heavy metals, certain stresses,
 such as hypoxemia (the dangerously low level of oxygen in the blood that
 occurs to some climbers at very high altitudes), may weaken this barrier.
 
 Silver is NOT a heavy metal, and CS has never been shown to cause argyria.
 Sigh...
 Marsha 


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CSOT hair color 4 gray hair OffTopic

2000-05-11 Thread Ritz3131
In a message dated 5/11/00 7:52:52 PM Pacific Daylight Time, 
mailer-dae...@aol.com writes:

 
 Hi.  I am wondering if people can tell me about safe forms of hair coloring. 
 
 I'm  only 30 but have some gray hair...actually they are white hairs...have 
 never seen a gray one. My dad got gray hair early and I think his mom did 
 so that is probably at least part of the cause. I am rifing and doing 
 supplements etc. but still have gray hairs.  I have tried lots of shades of 
 pure henna from the health food store and they do not bother me.  It is just 
 a powdered form of an herb and you ad water.  I have multiple chemical 
 sensitivities and I got another type of hair color from the health food 
store 
 that said natural on it and made from plants.  I bought this a long time ago 
 and never used it because I was trying various shades of henna.  Anyway, I 
 recently got it out to look at it and it does have lots of plant products in 
 it but some of the ingredients do not sound natural to me and I opened 2 
 bottles up and they smelled bad and made me nauseous.  The one bottle 
smelled 
 like finger nail polish or wine.  Anyway, the only problem with the henna is 
 that al the shades make my hair darker.  They cover up my natural highlights 
 and i think I look better with the blondish highlights which help bring out 
 my green eyes.  With the henna...even light brown...by light brown hair with 
 blondish highlights becomes what I call dark brown.  But, the company says 
 they cannot make blond henna b/c its not possible and they have tried.  With 
 henna it never lightens your hair.  It just coats it and helps cover the 
 gray.  Some products at walgreens you can get which won't lighten your hair 
 but will just cover it..so like you can get blond and the gray will become 
 blond...like Castings for example which you use like once a month.  But, I 
 opened that stuff up and smelled it and it stunk and made me nauseous.  So, 
I 
 just thought I would through this out their in case someone may know of 
 something I don't know about.  One company at a second health food store 
with 
 a different brand of henna has a blond henna but the ingredients actually 
 say neutral henna with chamomile and marigold herbs in the mix.  I did try 
it 
 just to see what would happen but it did not cover the gray at all.
 
 Thanks,
 
 Christy 

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From: ritz3...@aol.com
Message-ID: 92.4bb5087.264cc...@aol.com
Date: Thu, 11 May 2000 22:51:20 EDT
Subject: hair coloring to cover gray hair
To: rife-alt-hea...@topica.com
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MIME-Version: 1.0
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Content-Transfer-Encoding: 7bit
X-Mailer: AOL 4.0 for Windows 95 sub 100

Hi.  I am wondering if people can tell me about safe forms of hair coloring.  
I'm  only 30 but have some gray hair...actually they are white hairs...have 
never seen a gray one. My dad got gray hair early and I think his mom did 
so that is probably at least part of the cause. I am rifing and doing 
supplements etc. but still have gray hairs.  I have tried lots of shades of 
pure henna from the health food store and they do not bother me.  It is just 
a powdered form of an herb and you ad water.  I have multiple chemical 
sensitivities and I got another type of hair color from the health food store 
that said natural on it and made from plants.  I bought this a long time ago 
and never used it because I was trying various shades of henna.  Anyway, I 
recently got it out to look at it and 

Re: CSExcessweatinginfectionsLyme?

2000-05-07 Thread Ritz3131
Mycoplasma fermentans incognitus and also HIV I believe as well as TB can 
cause night sweats.  Maybe other infections do also.Anyone know if Lyme does?

Christy

n a message dated 5/7/00 10:14:21 AM Pacific Daylight Time, l...@fbtc.net 
writes:

 Subj: Re: CSExcessive sweating
 Date:  5/7/00 10:14:21 AM Pacific Daylight Time
 From:  l...@fbtc.net (Tai-Pan)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Kathy,
 
  Here is more info relevant to sweating.
 
  Sometimes a deficiency in vitamin B12 and zinc can contribute to excess 
sweating.
 
  Another possibility is low nicotinic acid (Niacin). The body makes its own 
niacin
 from the amino acid tryptophan. Your body can not do it if you are deficient 
in B1,
 B2, and B6.
 
 Profuse sweating can be a sign of infection, heart disease, an over active 
thyroid
 or the onset of tuberculosis.
 
  Possible Homeopathy remedies are acidum hydrofluoricum, silicea, calcarea, 
these
 are available at health food stores.
 
  Another possibility is enzyme deficiency, consult a good book on enzyme 
therapy or
 see a practitioner. Enzyme problems are usually connected with thyroid 
disorders,
 which in turn affect the skin and sweat glands.
 
 A useful herbal powder can be prepared using tree tea oil and ginger powder.
 Inclusion of lavender essential oil will give it a nice fragrance.
  Here is how to do it. In a large jar combine 1/2 cup powdered arrowroot, 
1/2 cup
 of cosmetic clay, 2 tablespoons of powdered ginger. Shake to mix, add 20 
drops of
 tree tea oil or /and lavender essential oil and shake again. You may want to 
put it
 through a fine mesh strainer to eliminate any clumps. Store in a dark 
covered jar.
 
   Bless youBob Lee 


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CSMSM-age spots?

2000-05-04 Thread Ritz3131
I wonder if that would work for age spots also?

Christy

In a message dated 5/2/00 9:49:42 PM Pacific Daylight Time, a...@trail.com 
writes:

 I have however
 sprayed a mixture of MSM on a pre-cancerous neoplasm near my eye , and
 gotten it in the eye without discomfort.  I have been doing this for about 3
 months.  The weird spot, diagnosed by both a GP and a Dermatolgist, is
 fading away.  I suspect if I used a small adhesive bandage and kept it
 moist, that the result would happen much faster, but I don't like the effect
 of the adhesive on my skin, which I think is a toxic reaction both to being
 sealed from the air, and the glue itself.
 
 The original most common route of administration of CS when used in the '20s
 and 30's was intravenous.
 
 James Osbourne Holmes
 
 FTNWO
  


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Re: CS and HIV

2000-05-04 Thread Ritz3131
HI.  I was wondering how much you are taking of the CS and how many times a 
day.  Also, when in January did you start it and when was your blood drawn 
for the tests?  Do you know what parts per million you are taking.

It sounds like there has been improvement so that is good!!  I would NOT 
assume you have reached a plateau b/c people with other chronic infections 
like Lyme from what I understand I believe slowly improve over many months 
for example.

I would not be too excited about prescription drugs for AIDS.

Keep with the CS and possibly increase?

Also, you may want to check out www.sota-inc.com and also look into rifing 
just in case you may be interested.  To start looking into that go to 
www.rt66.com/~rifetech/ and follow the links.

Best wishes.  Hang in there and don't give up.  It sounds like you are making 
progress.

Christy

n a message dated 5/3/00 7:55:59 AM Pacific Daylight Time, 
corni...@hotmail.com writes:

 Subj: CS and HIV
 Date:  5/3/00 7:55:59 AM Pacific Daylight Time
 From:  corni...@hotmail.com (Chad Powell)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Hey, Listers...
 
 I have been part of this list for a few months now.  I have HIV, and I 
 turned to CS to see what the effects would be for me.  I went to get my 
 results yesterday from my lab tests after using the CS since January.  I 
 talked to my doctor very briefly about CS.  He's trying to warn me about the 
 long term side effects.  Then again, no one knows the long term effects of 
 the HIV drugs, either.
 
 Anyway.  My viral load the last time I was tested was at 22,000 copies per 
 CC of blood, and my T-Cell count was at 598.  This time my T-cell count was 
 594 and my viral load was at 16,000 copies per CC of blood.  Not the changes 
 I was expecting, by any means.  It was a good sign that the viral load went 
 down, but it was not as low as I was thinking the CS would get it to.  The 
 questions I am thinking of now...was the CS effective in slowly bringing my 
 load down, or has my body hit a plateau for the time being, and is it 
 successfully holding off the virus right now?  I am not sure what to think 
 or believe.  I am not too concerned about the viral load right now, unless 
 it gets up over 20,000 again.  I should be fine until then because my T-Cell 
 count is high.  The next question isdo I just continue taking the CS, or 
 do I begin taking the medications that will get my viral load down to 
 undetectable?
 
 Kinda crazy.  I am at a loss what to think or do right now.  I am 
 disapointed, but I have to continue the fight.  Let me know what you think. 



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CSTests 4 Lyme OT

2000-04-27 Thread Ritz3131
Hi.  I am just curious what tests the lyme patients have had for Lyme and 
which are reliable.

Thanks,

Christy


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Re: CSHow shoud Cs be used for asthma?

2000-04-20 Thread Ritz3131
Hi Marsha,

I didn't know you had Lyme.  Did antibiotics get you over that?  Do you think 
the asthma in part was a result of the lyme?

Take care,

Christy
In a message dated 4/19/00 3:51:20 PM Pacific Daylight Time, 
liah...@pacbell.net writes:

 
 Dear Christy, I have only been living here for 17 months. She was sick long
 before that, first becoming ill at 21 or so.  I have wondered if she didn`t
 have Lyme Disease originally, from ticks in Idaho where we grew up. She was
 outdoorsy, I`m not. More a book person...
 I got my Lyme in Arkansas, from deer ticks in the backyard.
 I have no idea about the bugs you mention.
 Marsha 


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Re: CSHow shoud Cs be used for asthma?

2000-04-19 Thread Ritz3131
Hi Marsha,

That is great to hear.  What Parts Per Million do you use?  Do you make your 
own?  Suggest any machines one can buy?  Do you take it daily?  How much do 
you take? Do you not normally take it orally...do you take it with a 
neublizer sometimes?  How long have you been taking it?

also, with the asthma did you notice you where more short of breath in a warm 
environment and could breath easier in a fairly cool environment?  Did you 
also notice that drinking lots of water...especially cool water helped you to 
be able to breath easier?  Did you also notice that if it was kind of warm in 
your house etc. and you were talking for a while you would get quite out of 
breath?

thanks so much,

Christy



In a message dated 4/18/00 4:01:16 PM Pacific Daylight Time, 
liah...@pacbell.net writes:

 Subj: Re: CSHow shoud Cs be used for asthma?
 Date:  4/18/00 4:01:16 PM Pacific Daylight Time
 From:  liah...@pacbell.net (Marsha Hallett)
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 
 
  I would also like to know about this.
 
  Thanks,
 
  Christy
   Recently someone mentioned how Cs needs to be used in the best way for
 the
   best results.  How should it be used for asthma?
   Karen 
 
 Dear Christy and Karen, I used to be asthmatic, mainly it was allergic
 reactions. Since good old CS came into my life, I no longer get attacks,
 just a few wheezes occasionally. When that happens, I take more CS by mouth,
 and it goes away. One can also put it up the nose using an empty saline
 spritzer.
 I love this stuff!
 My current eye infection is nearly gone, after two doses of CS in the eye.
 Marsha 


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Re: CSHow shoud Cs be used for asthma?

2000-04-19 Thread Ritz3131
Marsha,

I was just curious when you got the asthma and when your sister got sick and 
if you had much contact.  I was thinking maybe you both could have been 
infected with a pathogenic strain of mycoplasma or Chlamydia pneumonia or 
something since these hare being associated with these types of illness by 
some researchers.


Take care,

Christy
  n a message dated 4/18/00 9:48:17 PM Pacific Daylight Time, 
liah...@pacbell.net writes:

 I`ve been taking CS off and on for 4 years come
 May.  I haven`t used a nebulizer, don`t have one. My sister, who has MS,
 insulin-dependant diabetes, and lung disease from second-hand smoke and
 chemicals at work, and is now totally disabled at age 58, won`t even try CS 



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Re: CSallergic reactions

2000-04-19 Thread Ritz3131
Rapid heart beat or palpitations is a herx/die off symptoms for me with 
antibiotics as well as rifing and I know others who report the same thing.  
it decreases and then goes away with time.

Christy

In a message dated 4/19/00 8:39:43 AM Pacific Daylight Time, 
mdev...@mail.id.net writes:

 She had all the classic symptoms of allergic reaction -- rapid 
 heartbeat, shortness of breath, low blood pressure (dizziness and 
 tunnel vision), etc... 


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Re: CSHow shoud Cs be used for asthma?

2000-04-18 Thread Ritz3131
I would also like to know about this.

Thanks,

Christy

n a message dated 4/18/00 5:13:43 AM Pacific Daylight Time, fernwo...@aol.com 
writes:

 Subj: CSHow shoud Cs be used for asthma?
 Date:  4/18/00 5:13:43 AM Pacific Daylight Time
 From:  fernwo...@aol.com
 Reply-to:  silver-list@eskimo.com
 To:silver-list@eskimo.com
 
 Recently someone mentioned how Cs needs to be used in the best way for the 
 best results.  How should it be used for asthma?  
 Karen 


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