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#87088 From: Susan Siegel <ssiegel5@...>
Date: Tue Nov 10, 2009 1:53 am
Subject: Re: no teasel theripist 		ssiegel921
Offline Offline
Send Email Send Email
 
FWIW- For what it;s worth
She is in my area (D.C.).  We have used her for in office and distance treatments.  We bought the kit and do our own treatments at home.  She was trained by Delta Gardens.

Susan 

On Nov 9, 2009, at 8:00 PM, Sandra Gikas wrote:



what does FWIW stand for?  BTW- where did you find your teasel therapist?  What area?  Was she referred to you by Delta?
 
Sandra
----- Original Message -----
Sent: Monday, November 09, 2009 7:32 PM
Subject: Re: [lymestrategies] no teasel theripist

I sought out this treatment specifically for babesia and it did work, FWIW.

Susan 

On Nov 9, 2009, at 3:34 PM, Tess Gomez wrote:



 
I'm about to start the teasel therapy, and the therapist I talked to told me that Babesia which is one of my co-infections, could interfere with the success of this therapy since Babesia is not caused by bacteria but by protozoan, so I'm wondering if I should wait until babesia is out of the picture.
Any comments about this would be appreciated. Thank you.
 
Tess


--- On Mon, 11/9/09, Susan Siegel <ssiegel5@verizon.net> wrote:

From: Susan Siegel <ssiegel5@verizon.net>
Subject: Re: [lymestrategies] no teasel theripist
To: lymestrategies@yahoogroups.com
Date: Monday, November 9, 2009, 8:05 PM

Call my practitioner.  She does distance sessions.  Me, my husband,  
and my daughter have all done this with success.

Trish Mooney
http://www.rockwaterhealing.com/
  (301) 996-5656

Susan

On Nov 9, 2009, at 2:55 PM, bacwannaski wrote:

> non s/c well delta gardens left me a message on my phone and said  
> there is no theripist in my area im waiting to here from sue massie  
> I missed her the first time she called.I am so depresed I feel my  
> lyme is gettinhg worse the  s/c had stoped makeing me improve but I  
> think it was stoping me from getting worse now I can,t take it cause  
> I can,t drink that much water now I hope there is other hope out  
> there for me just unlodeing .Becky
>
>
>
> ------------------------------------
>
> The information anywhere on Lyme Strategies should not be considered  
> complete, nor should it be relied on or interpreted to suggest a  
> course of treatment for any individual.  It is research information  
> only and it should not be used in place of a visit, call,  
> consultation or the advice of your physician or other qualified  
> health care provider.  Information obtained with regards to Lyme  
> Strategies is research only on an ongoing basis for review and  
> evaluation.  Any application or implementation of research  
> information is considered at the members own risk.  The providers of  
> the Lyme Strategies site are not medical physicians.  Should you  
> have any health care-related questions, please call or see your  
> physician or other qualified health care provider promptly. Yahoo!  
> Groups Links
>
>
>



------------------------------------

The information anywhere on Lyme Strategies should not be considered complete, nor should it be relied on or interpreted to suggest a course of treatment for any individual.  It is research information only and it should not be used in place of a visit, call, consultation or the advice of your physician or other qualified health care provider.  Information obtained with regards to Lyme Strategies is research only on an ongoing basis for review and evaluation.  Any application or implementation of research information is considered at the members own risk.  The providers of the Lyme Strategies site are not medical physicians.  Should you have any health care-related questions, please call or see your physician or other qualified health care provider promptly. Yahoo! Groups Links

<*> To visit your group on the web, go to:
    http://groups.yahoo.com/group/lymestrategies/

<*> Your email settings:
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<*> To change settings online go to:
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Reply | Forward | Messages in this Topic (38)
#87087 From: Suemassie45@...
Date: Mon Nov 9, 2009 8:47 pm
Subject: Re:no teasel theripist 		sueinnj44
Offline Offline
Send Email Send Email
 
non s/c well delta gardens left me a message on my phone and said there is no theripist in my area im waiting to here from sue massie I missed her the first time she called.I am so depresed I feel my lyme is gettinhg worse the s/c had stoped makeing me improve but I think it was stoping me from getting worse now I can,t take it cause I can,t drink that much water now I hope there is other hope out there for me just unlodeing .Becky
***************
Becky-
I will call you again tomorrow afternoon (Tues); I was in PA today at an appt. Just wanted to let you know.
 
blessings-

Dr. Sue Massie
732 933 4011

Reply | Forward | Messages in this Topic (38)
#87086 From: "haecklers" <haecklers@...>
Date: Tue Nov 10, 2009 1:43 am
Subject: Re: Non S/C:Desperate Coconut oil for Inflammation?, Type of Iodine for Thyroid? 		haecklers
Offline Offline
Send Email Send Email
  
DMSO is wonderful for inflammation.  It scavenges hydroxyl free radicals. 
You'll want to read up on its use as it's a solvent and you have to be careful
when using it but it's no big deal really.  It's a different form of NSAID (like
ibuprophen only it doesn't harm the digestive system - rather it helps it) but
it still relieves inflammation and pain as well as promoting healing in some
amazing ways.

You may be suffering some food sensitivities as well - lyme and candida both
promote leaky gut which causes food sensitivities when the undigested protein
particles leak into the blood stream and cause an immune response.  This causes
a lot of inflammation.  DMSO again is good for this; also some people get a
2-day cure using melatonin, which may be useful to you anyways since it helps
you sleep (is that one of your problems?)  Other things you can try are
eliminating your favorite foods (unfortunately the ones you crave are often the
ones you shouldn't eat - due to tolerance).  Likely culprits are dairy, eggs,
wheat, and chocolate.  An alternative to an elimination diet is Peptizyde by
Houston Nutriceuticals (you can google it).

Dr. Wong has a theory that a lot of the pain and other problems with
fibromyalgia are from low tryptophan, and says people who take tryptophan get
some pretty good relief from the pain and fatigue.

Another treatment that some claim is very helpful is taking D-ribose, which is a
Krebs Cycle type fuel that goes directly to the cells for cellular energy - one
of the theories of fibro. is that the Krebs cycle is interrupted.

I hope some of this helps.

--- In lymestrategies@yahoogroups.com, "lymegal2008" <dwrocket-lyme@...> wrote:
>
> Hi.
>
> PLEASE HELP. I am really  needing help with pain and fatigue, and have read
that pain is caused by inflammation.
>
> I made this post a few days ago and have only received one response. I do
appreciate the response I have gotten.
>
> However, is there anyone out there that can provide more information on how to
get rid of inflammation (and hopefully severe pain).
>
> Is coconut good for this.  If so, how do you take, what brand is good, etc.
>
> Please note that I also suffer from Candida, Lyme, Fibro (which is part of
Lyme, although my rheumo thinks otherwise), Severe pain and fatigue, being
bedridden, depression, anxiety, etc etc etc.  I'm sure I'm not the only one
going thru this.
>
>
> I am so in desperate need of help.  My marriage is falling apart, my 5 year
old only knows a sick Mommy, I am basically homebound, my life feel worthless
and empty.
>
> So, if anyone can PLEASE help, I'd greatly appreciate it.
>
> Lyme Gal
>
>
>
>
>
>
> --- In lymestrategies@yahoogroups.com, "lymegal2008" <dwrocket-lyme@> wrote:
> >
> > Hi, it's Lymegal.
> >
> > I'm trying to remember sometime back about help for inflammation and iodine
> >
> > I have a couple of questions?
> > 1.  I've read that Coconut Oil is good for things like Candida and
inflammation?  Has anyone else heard of this? And if so, what do I need to look
for Brand/Type/How Much
> >
> > 2. I did an Iodine patch test at with my nutrionist, and it came back really
just where I may need a little iodine.  Can someone guide me or provide links as
to what type of Iodine might be helpful (such as the kind he did my patch test
with) instead of a pill, and maybe a link to Home Iodine Treatment?  I don't
want to take any more pills. He's focusing right now on my cortisol, iron,
adrenals, etc.  So, I'm on quite a few tablets from Standard Process.
> >
> > He's a good guy and knows what he's doing, so I am willing to give this a
shot for the next month or so.  Thing is, I'm looking for lower cost
alternatives when I run out.
> >
> > I need to order my magnesium as I am almost out, so I'd like to add the
coconut oil, once I've heard to see if it does help with the inflammation.  And
I also am looking to get rid of my fatigue.
> >
> > You may remember my post a couple of weeks ago about the horrible pain,
fatigue, etc from Lyme and Fibro.
> >
> > My Lyme brain made me forget that inflammation causes the pain.  DUH.
> > So that's why I'm looking at something for inflammation.
> >
> > So, any advice would be greatly appreciaed again!
> >
> > LymeGal
> >
>

Reply | Forward | Messages in this Topic (14)
#87085 From: Sharon Tierney <stierney_23@...>
Date: Tue Nov 10, 2009 1:10 am
Subject: Re: Re: Non S/C:Desperate Coconut oil for Inflammation?, Type of Iodine for Thyroid? 		stierney_23
Offline Offline
Send Email Send Email
 
Cumanda from Nutramedix is really helping my friend with inflammation.  If you call Nutramedix they also have an entire protocol that has helped many.  My LLMD recommends this line of products and I am considering this as well.   Oil of Oregano from North American Herb and Spice helps some with inflammation.
Sharon T.
 
--- On Mon, 11/9/09, Meredith W. <meredithbw@...> wrote:

From: Meredith W. <meredithbw@...>
Subject: Re: [lymestrategies] Re: Non S/C:Desperate Coconut oil for Inflammation?, Type of Iodine for Thyroid?
To: lymestrategies@yahoogroups.com
Date: Monday, November 9, 2009, 7:59 PM

 

maybe look into curcumin.... .and dissolve in warn fat - like cream as its fat soluble ....hope you feel better

On Mon, Nov 9, 2009 at 10:53 PM, lymegal2008 <dwrocket-lyme@ yahoo.com> wrote:
 

Hi.

PLEASE HELP. I am really needing help with pain and fatigue, and have read that pain is caused by inflammation.

I made this post a few days ago and have only received one response. I do appreciate the response I have gotten.

However, is there anyone out there that can provide more information on how to get rid of inflammation (and hopefully severe pain).

Is coconut good for this. If so, how do you take, what brand is good, etc.

Please note that I also suffer from Candida, Lyme, Fibro (which is part of Lyme, although my rheumo thinks otherwise), Severe pain and fatigue, being bedridden, depression, anxiety, etc etc etc. I'm sure I'm not the only one going thru this.

I am so in desperate need of help. My marriage is falling apart, my 5 year old only knows a sick Mommy, I am basically homebound, my life feel worthless and empty.

So, if anyone can PLEASE help, I'd greatly appreciate it.

Lyme Gal

--- In lymestrategies@ yahoogroups. com, "lymegal2008" <dwrocket-lyme@ ...> wrote:
>
> Hi, it's Lymegal.
>
> I'm trying to remember sometime back about help for inflammation and iodine
>
> I have a couple of questions?
> 1. I've read that Coconut Oil is good for things like Candida and inflammation? Has anyone else heard of this? And if so, what do I need to look for Brand/Type/How Much
>
> 2. I did an Iodine patch test at with my nutrionist, and it came back really just where I may need a little iodine. Can someone guide me or provide links as to what type of Iodine might be helpful (such as the kind he did my patch test with) instead of a pill, and maybe a link to Home Iodine Treatment? I don't want to take any more pills. He's focusing right now on my cortisol, iron, adrenals, etc. So, I'm on quite a few tablets from Standard Process.
>
> He's a good guy and knows what he's doing, so I am willing to give this a shot for the next month or so. Thing is, I'm looking for lower cost alternatives when I run out.
>
> I need to order my magnesium as I am almost out, so I'd like to add the coconut oil, once I've heard to see if it does help with the inflammation. And I also am looking to get rid of my fatigue.
>
> You may remember my post a couple of weeks ago about the horrible pain, fatigue, etc from Lyme and Fibro.
>
> My Lyme brain made me forget that inflammation causes the pain. DUH.
> So that's why I'm looking at something for inflammation.
>
> So, any advice would be greatly appreciaed again!
>
> LymeGal
>




Reply | Forward | Messages in this Topic (14)
#87084 From: "Meredith W." <meredithbw@...>
Date: Tue Nov 10, 2009 12:59 am
Subject: Re: Re: Non S/C:Desperate Coconut oil for Inflammation?, Type of Iodine for Thyroid? 		mbshortsqueeze
Offline Offline
Send Email Send Email
 
maybe look into curcumin.....and dissolve in warn fat - like cream as its fat soluble ....hope you feel better

On Mon, Nov 9, 2009 at 10:53 PM, lymegal2008 <dwrocket-lyme@...> wrote:
 

Hi.

PLEASE HELP. I am really needing help with pain and fatigue, and have read that pain is caused by inflammation.

I made this post a few days ago and have only received one response. I do appreciate the response I have gotten.

However, is there anyone out there that can provide more information on how to get rid of inflammation (and hopefully severe pain).

Is coconut good for this. If so, how do you take, what brand is good, etc.

Please note that I also suffer from Candida, Lyme, Fibro (which is part of Lyme, although my rheumo thinks otherwise), Severe pain and fatigue, being bedridden, depression, anxiety, etc etc etc. I'm sure I'm not the only one going thru this.

I am so in desperate need of help. My marriage is falling apart, my 5 year old only knows a sick Mommy, I am basically homebound, my life feel worthless and empty.

So, if anyone can PLEASE help, I'd greatly appreciate it.

Lyme Gal

--- In lymestrategies@yahoogroups.com, "lymegal2008" <dwrocket-lyme@...> wrote:
>
> Hi, it's Lymegal.
>
> I'm trying to remember sometime back about help for inflammation and iodine
>
> I have a couple of questions?
> 1. I've read that Coconut Oil is good for things like Candida and inflammation? Has anyone else heard of this? And if so, what do I need to look for Brand/Type/How Much
>
> 2. I did an Iodine patch test at with my nutrionist, and it came back really just where I may need a little iodine. Can someone guide me or provide links as to what type of Iodine might be helpful (such as the kind he did my patch test with) instead of a pill, and maybe a link to Home Iodine Treatment? I don't want to take any more pills. He's focusing right now on my cortisol, iron, adrenals, etc. So, I'm on quite a few tablets from Standard Process.
>
> He's a good guy and knows what he's doing, so I am willing to give this a shot for the next month or so. Thing is, I'm looking for lower cost alternatives when I run out.
>
> I need to order my magnesium as I am almost out, so I'd like to add the coconut oil, once I've heard to see if it does help with the inflammation. And I also am looking to get rid of my fatigue.
>
> You may remember my post a couple of weeks ago about the horrible pain, fatigue, etc from Lyme and Fibro.
>
> My Lyme brain made me forget that inflammation causes the pain. DUH.
> So that's why I'm looking at something for inflammation.
>
> So, any advice would be greatly appreciaed again!
>
> LymeGal
>



Reply | Forward | Messages in this Topic (14)
#87083 From: "Sandra Gikas" <skg59@...>
Date: Tue Nov 10, 2009 1:00 am
Subject: Re: no teasel theripist 		gikassandra
Offline Offline
Send Email Send Email
 
what does FWIW stand for?  BTW- where did you find your teasel therapist?  What area?  Was she referred to you by Delta?
 
Sandra
----- Original Message -----
Sent: Monday, November 09, 2009 7:32 PM
Subject: Re: [lymestrategies] no teasel theripist

 

I sought out this treatment specifically for babesia and it did work, FWIW.

Susan 

On Nov 9, 2009, at 3:34 PM, Tess Gomez wrote:



 
I'm about to start the teasel therapy, and the therapist I talked to told me that Babesia which is one of my co-infections, could interfere with the success of this therapy since Babesia is not caused by bacteria but by protozoan, so I'm wondering if I should wait until babesia is out of the picture.
Any comments about this would be appreciated. Thank you.
 
Tess


--- On Mon, 11/9/09, Susan Siegel <ssiegel5@verizon.net> wrote:

From: Susan Siegel <ssiegel5@verizon.net>
Subject: Re: [lymestrategies] no teasel theripist
To: lymestrategies@yahoogroups.com
Date: Monday, November 9, 2009, 8:05 PM

Call my practitioner.  She does distance sessions.  Me, my husband,  
and my daughter have all done this with success.

Trish Mooney
http://www.rockwaterhealing.com/
  (301) 996-5656

Susan

On Nov 9, 2009, at 2:55 PM, bacwannaski wrote:

> non s/c well delta gardens left me a message on my phone and said  
> there is no theripist in my area im waiting to here from sue massie  
> I missed her the first time she called.I am so depresed I feel my  
> lyme is gettinhg worse the  s/c had stoped makeing me improve but I  
> think it was stoping me from getting worse now I can,t take it cause  
> I can,t drink that much water now I hope there is other hope out  
> there for me just unlodeing .Becky
>
>
>
> ------------------------------------
>
> The information anywhere on Lyme Strategies should not be considered  
> complete, nor should it be relied on or interpreted to suggest a  
> course of treatment for any individual.  It is research information  
> only and it should not be used in place of a visit, call,  
> consultation or the advice of your physician or other qualified  
> health care provider.  Information obtained with regards to Lyme  
> Strategies is research only on an ongoing basis for review and  
> evaluation.  Any application or implementation of research  
> information is considered at the members own risk.  The providers of  
> the Lyme Strategies site are not medical physicians.  Should you  
> have any health care-related questions, please call or see your  
> physician or other qualified health care provider promptly. Yahoo!  
> Groups Links
>
>
>



------------------------------------

The information anywhere on Lyme Strategies should not be considered complete, nor should it be relied on or interpreted to suggest a course of treatment for any individual.  It is research information only and it should not be used in place of a visit, call, consultation or the advice of your physician or other qualified health care provider.  Information obtained with regards to Lyme Strategies is research only on an ongoing basis for review and evaluation.  Any application or implementation of research information is considered at the members own risk.  The providers of the Lyme Strategies site are not medical physicians.  Should you have any health care-related questions, please call or see your physician or other qualified health care provider promptly. Yahoo! Groups Links

<*> To visit your group on the web, go to:
    http://groups.yahoo.com/group/lymestrategies/

<*> Your email settings:
    Individual Email | Traditional

<*> To change settings online go to:
    http://groups.yahoo.com/group/lymestrategies/join
    (Yahoo! ID required)

<*> To change settings via email:
    lymestrategies-digest@yahoogroups.com 
    lymestrategies-fullfeatured@yahoogroups.com

<*> To unsubscribe from this group, send an email to:
    lymestrategies-unsubscribe@yahoogroups.com

<*> Your use of Yahoo! Groups is subject to:
    http://docs.yahoo.com/info/terms/






Reply | Forward | Messages in this Topic (38)
#87082 From: "lymegal2008" <dwrocket-lyme@...>
Date: Tue Nov 10, 2009 12:53 am
Subject: Re: Non S/C:Desperate Coconut oil for Inflammation?, Type of Iodine for Thyroid? 		lymegal2008
Offline Offline
Send Email Send Email
  
Hi.

PLEASE HELP. I am really  needing help with pain and fatigue, and have read that
pain is caused by inflammation.

I made this post a few days ago and have only received one response. I do
appreciate the response I have gotten.

However, is there anyone out there that can provide more information on how to
get rid of inflammation (and hopefully severe pain).

Is coconut good for this.  If so, how do you take, what brand is good, etc.

Please note that I also suffer from Candida, Lyme, Fibro (which is part of Lyme,
although my rheumo thinks otherwise), Severe pain and fatigue, being bedridden,
depression, anxiety, etc etc etc.  I'm sure I'm not the only one going thru
this.


I am so in desperate need of help.  My marriage is falling apart, my 5 year old
only knows a sick Mommy, I am basically homebound, my life feel worthless and
empty.

So, if anyone can PLEASE help, I'd greatly appreciate it.

Lyme Gal






--- In lymestrategies@yahoogroups.com, "lymegal2008" <dwrocket-lyme@...> wrote:
>
> Hi, it's Lymegal.
>
> I'm trying to remember sometime back about help for inflammation and iodine
>
> I have a couple of questions?
> 1.  I've read that Coconut Oil is good for things like Candida and
inflammation?  Has anyone else heard of this? And if so, what do I need to look
for Brand/Type/How Much
>
> 2. I did an Iodine patch test at with my nutrionist, and it came back really
just where I may need a little iodine.  Can someone guide me or provide links as
to what type of Iodine might be helpful (such as the kind he did my patch test
with) instead of a pill, and maybe a link to Home Iodine Treatment?  I don't
want to take any more pills. He's focusing right now on my cortisol, iron,
adrenals, etc.  So, I'm on quite a few tablets from Standard Process.
>
> He's a good guy and knows what he's doing, so I am willing to give this a shot
for the next month or so.  Thing is, I'm looking for lower cost alternatives
when I run out.
>
> I need to order my magnesium as I am almost out, so I'd like to add the
coconut oil, once I've heard to see if it does help with the inflammation.  And
I also am looking to get rid of my fatigue.
>
> You may remember my post a couple of weeks ago about the horrible pain,
fatigue, etc from Lyme and Fibro.
>
> My Lyme brain made me forget that inflammation causes the pain.  DUH.
> So that's why I'm looking at something for inflammation.
>
> So, any advice would be greatly appreciaed again!
>
> LymeGal
>

Reply | Forward | Messages in this Topic (14)
#87081 From: Susan Siegel <ssiegel5@...>
Date: Tue Nov 10, 2009 12:32 am
Subject: Re: no teasel theripist 		ssiegel921
Offline Offline
Send Email Send Email
 
I sought out this treatment specifically for babesia and it did work, FWIW.
Susan 

On Nov 9, 2009, at 3:34 PM, Tess Gomez wrote:



 
I'm about to start the teasel therapy, and the therapist I talked to told me that Babesia which is one of my co-infections, could interfere with the success of this therapy since Babesia is not caused by bacteria but by protozoan, so I'm wondering if I should wait until babesia is out of the picture.
Any comments about this would be appreciated. Thank you.
 
Tess


--- On Mon, 11/9/09, Susan Siegel <ssiegel5@...> wrote:

From: Susan Siegel <ssiegel5@...>
Subject: Re: [lymestrategies] no teasel theripist
To: lymestrategies@yahoogroups.com
Date: Monday, November 9, 2009, 8:05 PM

Call my practitioner.  She does distance sessions.  Me, my husband,  
and my daughter have all done this with success.

Trish Mooney
http://www.rockwaterhealing.com/
  (301) 996-5656

Susan

On Nov 9, 2009, at 2:55 PM, bacwannaski wrote:

> non s/c well delta gardens left me a message on my phone and said  
> there is no theripist in my area im waiting to here from sue massie  
> I missed her the first time she called.I am so depresed I feel my  
> lyme is gettinhg worse the  s/c had stoped makeing me improve but I  
> think it was stoping me from getting worse now I can,t take it cause  
> I can,t drink that much water now I hope there is other hope out  
> there for me just unlodeing .Becky
>
>
>
> ------------------------------------
>
> The information anywhere on Lyme Strategies should not be considered  
> complete, nor should it be relied on or interpreted to suggest a  
> course of treatment for any individual.  It is research information  
> only and it should not be used in place of a visit, call,  
> consultation or the advice of your physician or other qualified  
> health care provider.  Information obtained with regards to Lyme  
> Strategies is research only on an ongoing basis for review and  
> evaluation.  Any application or implementation of research  
> information is considered at the members own risk.  The providers of  
> the Lyme Strategies site are not medical physicians.  Should you  
> have any health care-related questions, please call or see your  
> physician or other qualified health care provider promptly. Yahoo!  
> Groups Links
>
>
>



------------------------------------

The information anywhere on Lyme Strategies should not be considered complete, nor should it be relied on or interpreted to suggest a course of treatment for any individual.  It is research information only and it should not be used in place of a visit, call, consultation or the advice of your physician or other qualified health care provider.  Information obtained with regards to Lyme Strategies is research only on an ongoing basis for review and evaluation.  Any application or implementation of research information is considered at the members own risk.  The providers of the Lyme Strategies site are not medical physicians.  Should you have any health care-related questions, please call or see your physician or other qualified health care provider promptly. Yahoo! Groups Links

<*> To visit your group on the web, go to:
    http://groups.yahoo.com/group/lymestrategies/

<*> Your email settings:
    Individual Email | Traditional

<*> To change settings online go to:
    http://groups.yahoo.com/group/lymestrategies/join
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Reply | Forward | Messages in this Topic (38)
#87080 From: "Sandra Gikas" <skg59@...>
Date: Mon Nov 9, 2009 10:35 pm
Subject: Re: Re: non S/C: Colloidal Silver ? 		gikassandra
Offline Offline
Send Email Send Email
 
Do you know if she had any co-infections?
 
Sandra
----- Original Message -----
Sent: Monday, November 09, 2009 4:50 PM
Subject: RE: [lymestrategies] Re: non S/C: Colloidal Silver ?

 

Hi!

I had not seen your posts before sorry or I would have responded.

My wife has successfully used CS/C to help her healing from Chronic Lyme. In
general it seems to put the lyme into remission and after awhile there is
limited Herxing. It wasn't until she started adding Rifing to the mix last
month that Herxes started up again. She felt she was already back at 90%
health using just the CS/C at that point.

Lots of information about CS, Salt/C and other treatments on my free Lyme
resource CD.

Scott Adams
www.lyme-resource.com
You can lead a person to a fact, but you can't make them think! - Scott
Adams


> -----Original Message-----
> From: lymestrategies@yahoogroups.com
> [mailto:lymestrategies@yahoogroups.com] On Behalf Of harmonyetc
> Sent: Monday, November 09, 2009 2:45 PM
> To: lymestrategies@yahoogroups.com
> Subject: [lymestrategies] Re: non S/C: Colloidal Silver ?
>
> Evidently it is very difficult to get in on this tight knit
> group as I've tried more than once with little or no response
> to my questions.
>
> I must not be asking right or something so I'm back to
> lurking here and continuing to search for answers elsewhere.
> Blessings and healing to everyone here. K
>
> --- In lymestrategies@yahoogroups.com, "harmonyetc"
> <ekolsen5@...> wrote:
> >
> > I just took my first 2oz of colloidal silver this morning
> and will take 4 more oz spread throughout the day. Aside
> from having a headache and some dizziness I have not noticed
> anything else (thank goodness).
> >
> > Is this similar to what I can expect from this amount? I
> know everyone is different, but what I'm asking is more...
> Reaction that is OK ( I can tolerate) vs. bedridden herxing.
> >
> > I have an idea of how to support my detox pathways, but
> does anyone here have any added suggestions? I would greatly
> appreciate the help.
> >
>
>
>
>
> ------------------------------------
>
> The information anywhere on Lyme Strategies should not be
> considered complete, nor should it be relied on or
> interpreted to suggest a course of treatment for any
> individual. It is research information only and it should
> not be used in place of a visit, call, consultation or the
> advice of your physician or other qualified health care
> provider. Information obtained with regards to Lyme
> Strategies is research only on an ongoing basis for review
> and evaluation. Any application or implementation of
> research information is considered at the members own risk.
> The providers of the Lyme Strategies site are not medical
> physicians. Should you have any health care-related
> questions, please call or see your physician or other
> qualified health care provider promptly. Yahoo! Groups Links
>
>
>
>


Reply | Forward | Messages in this Topic (7)
#87079 From: "Nancy Wilson" <wilson33@...>
Date: Mon Nov 9, 2009 10:27 pm
Subject: RE: Re: non S/C: Colloidal Silver ? 		zoie19582002
Offline Offline
Send Email Send Email
 
Well said!

From: lymestrategies@yahoogroups.com [mailto:lymestrategies@yahoogroups.com] On Behalf Of mercurybeater
Sent: Monday, November 09, 2009 1:51 PM
To: lymestrategies@yahoogroups.com
Subject: [lymestrategies] Re: non S/C: Colloidal Silver ?

 

harmony etc
all i can say is that the herxing is very individual;

i know from rifing that the cumulative effect of rifing did not hit me for a week-10 days after i had dug myself a deep hole

I know having chelated for mercury using ALA that a similair thing happened..ie i was overdoing it and it took a week + for me to crash
severely

all i can say, is going slowly and taking a break from whatever kill mechanism you are using Ie rifing, CS, salt-C; would seem to the most appropriate

The time it will take for your body time to clear this die off and how severe the herx's will be, is dependent on how toxic you are
and how much you have killed..both of which is very indvidual

-,michael

--- In lymestrategies@yahoogroups.com, "harmonyetc" <ekolsen5@...> wrote:
>
> Evidently it is very difficult to get in on this tight knit group as I've tried more than once with little or no response to my questions.
>
> I must not be asking right or something so I'm back to lurking here and continuing to search for answers elsewhere. Blessings and healing to everyone here. K
>
> --- In lymestrategies@yahoogroups.com, "harmonyetc" <ekolsen5@> wrote:
> >
> > I just took my first 2oz of colloidal silver this morning and will take 4 more oz spread throughout the day. Aside from having a headache and some dizziness I have not noticed anything else (thank goodness).
> >
> > Is this similar to what I can expect from this amount? I know everyone is different, but what I'm asking is more... Reaction that is OK ( I can tolerate) vs. bedridden herxing.
> >
> > I have an idea of how to support my detox pathways, but does anyone here have any added suggestions? I would greatly appreciate the help.
> >
>


Reply | Forward | Messages in this Topic (7)
#87078 From: "mercurybeater" <mercurybeater@...>
Date: Mon Nov 9, 2009 9:50 pm
Subject: Re: non S/C: Colloidal Silver ? 		mercurybeater
Offline Offline
Send Email Send Email
  
harmony etc
all i can say is that the herxing is very individual;

i know from rifing that the cumulative effect of rifing did not hit me for a
week-10 days after i had dug myself a deep hole

I know having chelated for mercury using ALA that a similair thing happened..ie
i was overdoing it and it took a week + for me to crash
severely

all i can say, is going slowly and taking a break from whatever kill mechanism
you are using Ie rifing, CS, salt-C; would seem to the most appropriate

The time it will take for your body time to clear this die off and how severe
the herx's will be, is dependent on how toxic you are
and how much you have killed..both of which is very indvidual

-,michael


--- In lymestrategies@yahoogroups.com, "harmonyetc" <ekolsen5@...> wrote:
>
> Evidently it is very difficult to get in on this tight knit group as I've
tried more than once with little or no response to my questions.
>
> I must not be asking right or something so I'm back to lurking here and
continuing to search for answers elsewhere.  Blessings and healing to everyone
here.  K
>
> --- In lymestrategies@yahoogroups.com, "harmonyetc" <ekolsen5@> wrote:
> >
> > I just took my first 2oz of colloidal silver this morning and will take 4
more oz spread throughout the day.  Aside from having a headache and some
dizziness I have not noticed anything else (thank goodness).
> >
> > Is this similar to what I can expect from this amount?  I know everyone is
different, but what I'm asking is more... Reaction that is OK ( I can tolerate)
vs. bedridden herxing.
> >
> > I have an idea of how to support my detox pathways, but does anyone here
have any added suggestions?  I would greatly appreciate the help.
> >
>

Reply | Forward | Messages in this Topic (7)
#87077 From: "Scott Adams" <msadams@...>
Date: Mon Nov 9, 2009 9:50 pm
Subject: RE: Re: non S/C: Colloidal Silver ? 		msadams
Offline Offline
Send Email Send Email
  
Hi!

I had not seen your posts before sorry or I would have responded.

My wife has successfully used CS/C to help her healing from Chronic Lyme. In
general it seems to put the lyme into remission and after awhile there is
limited Herxing. It wasn't until she started adding Rifing to the mix last
month that Herxes started up again. She felt she was already back at 90%
health using just the CS/C at that point.

Lots of information about CS, Salt/C and other treatments on my free Lyme
resource CD.

Scott Adams
www.lyme-resource.com
You can lead a person to a fact, but you can't make them think! - Scott
Adams


> -----Original Message-----
> From: lymestrategies@yahoogroups.com
> [mailto:lymestrategies@yahoogroups.com] On Behalf Of harmonyetc
> Sent: Monday, November 09, 2009 2:45 PM
> To: lymestrategies@yahoogroups.com
> Subject: [lymestrategies] Re: non S/C: Colloidal Silver ?
>
> Evidently it is very difficult to get in on this tight knit
> group as I've tried more than once with little or no response
> to my questions.
>
> I must not be asking right or something so I'm back to
> lurking here and continuing to search for answers elsewhere.
> Blessings and healing to everyone here.  K
>
> --- In lymestrategies@yahoogroups.com, "harmonyetc"
> <ekolsen5@...> wrote:
> >
> > I just took my first 2oz of colloidal silver this morning
> and will take 4 more oz spread throughout the day.  Aside
> from having a headache and some dizziness I have not noticed
> anything else (thank goodness).
> >
> > Is this similar to what I can expect from this amount?  I
> know everyone is different, but what I'm asking is more...
> Reaction that is OK ( I can tolerate) vs. bedridden herxing.
> >
> > I have an idea of how to support my detox pathways, but
> does anyone here have any added suggestions?  I would greatly
> appreciate the help.
> >
>
>
>
>
> ------------------------------------
>
> The information anywhere on Lyme Strategies should not be
> considered complete, nor should it be relied on or
> interpreted to suggest a course of treatment for any
> individual.  It is research information only and it should
> not be used in place of a visit, call, consultation or the
> advice of your physician or other qualified health care
> provider.  Information obtained with regards to Lyme
> Strategies is research only on an ongoing basis for review
> and evaluation.  Any application or implementation of
> research information is considered at the members own risk.
> The providers of the Lyme Strategies site are not medical
> physicians.  Should you have any health care-related
> questions, please call or see your physician or other
> qualified health care provider promptly. Yahoo! Groups Links
>
>
>
>

Reply | Forward | Messages in this Topic (7)
#87076 From: "Cindi Callanan" <cindicallanan@...>
Date: Mon Nov 9, 2009 9:32 pm
Subject: Re: no teasel theripist 		cindi_callanan
Offline Offline
Send Email Send Email
 
Tess, I haven't gone through the teasel training yet (Nov. 21st!), and I would think it would help, regardless of whether you have babesia or not.  We have bartonella, babesia, and all sorts of other things, and it's been helping.  I'd ask Lindy at Delta Gardens what she thinks, too. 
 
Did you find someone in your area?  If not, you could start with the root first and follow with the complete essence protocol. 
 
Take good care,
 
Cindi
 
 
 
Cindi Callanan, MsT, CST, BEC
Power Wellness Solutions
Integrative Wellness Consultant/Health Coach
National Cleansing Coach
410-771-4994 O
443-980-7369 Cell
----- Original Message -----
From: Tess Gomez
Sent: Monday, November 09, 2009 3:34 PM
Subject: Re: [lymestrategies] no teasel theripist

 

 
I'm about to start the teasel therapy, and the therapist I talked to told me that Babesia which is one of my co-infections, could interfere with the success of this therapy since Babesia is not caused by bacteria but by protozoan, so I'm wondering if I should wait until babesia is out of the picture.
Any comments about this would be appreciated. Thank you.
 
Tess


--- On Mon, 11/9/09, Susan Siegel <ssiegel5@verizon.net> wrote:

From: Susan Siegel <ssiegel5@verizon.net>
Subject: Re: [lymestrategies] no teasel theripist
To: lymestrategies@yahoogroups.com
Date: Monday, November 9, 2009, 8:05 PM

Call my practitioner.  She does distance sessions.  Me, my husband, 
and my daughter have all done this with success.

Trish Mooney
http://www.rockwaterhealing.com/
  (301) 996-5656

Susan

On Nov 9, 2009, at 2:55 PM, bacwannaski wrote:

> non s/c well delta gardens left me a message on my phone and said 
> there is no theripist in my area im waiting to here from sue massie 
> I missed her the first time she called.I am so depresed I feel my 
> lyme is gettinhg worse the  s/c had stoped makeing me improve but I 
> think it was stoping me from getting worse now I can,t take it cause 
> I can,t drink that much water now I hope there is other hope out 
> there for me just unlodeing .Becky
>
>
>
> ------------------------------------
>
> The information anywhere on Lyme Strategies should not be considered 
> complete, nor should it be relied on or interpreted to suggest a 
> course of treatment for any individual.  It is research information 
> only and it should not be used in place of a visit, call, 
> consultation or the advice of your physician or other qualified 
> health care provider.  Information obtained with regards to Lyme 
> Strategies is research only on an ongoing basis for review and 
> evaluation.  Any application or implementation of research 
> information is considered at the members own risk.  The providers of 
> the Lyme Strategies site are not medical physicians.  Should you 
> have any health care-related questions, please call or see your 
> physician or other qualified health care provider promptly. Yahoo! 
> Groups Links
>
>
>



------------------------------------

The information anywhere on Lyme Strategies should not be considered complete, nor should it be relied on or interpreted to suggest a course of treatment for any individual.  It is research information only and it should not be used in place of a visit, call, consultation or the advice of your physician or other qualified health care provider.  Information obtained with regards to Lyme Strategies is research only on an ongoing basis for review and evaluation.  Any application or implementation of research information is considered at the members own risk.  The providers of the Lyme Strategies site are not medical physicians.  Should you have any health care-related questions, please call or see your physician or other qualified health care provider promptly. Yahoo! Groups Links

<*> To visit your group on the web, go to:
    http://groups.yahoo.com/group/lymestrategies/

<*> Your email settings:
    Individual Email | Traditional

<*> To change settings online go to:
    http://groups.yahoo.com/group/lymestrategies/join
    (Yahoo! ID required)

<*> To change settings via email:
    lymestrategies-digest@yahoogroups.com
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<*> To unsubscribe from this group, send an email to:
    lymestrategies-unsubscribe@yahoogroups.com

<*> Your use of Yahoo! Groups is subject to:
    http://docs.yahoo.com/info/terms/



Reply | Forward | Messages in this Topic (38)
#87075 From: "Sandra Gikas" <skg59@...>
Date: Mon Nov 9, 2009 9:32 pm
Subject: Re: no teasel theripist 		gikassandra
Offline Offline
Send Email Send Email
 
This works even if you have Babesia.  I personally know a man who was very ill for 7 years with tick born disease.  He had bartonella and babesia and got well with teasel therapy.  David Dalton treated him directly though (that's a big plus) although there are many other great practitioners out there who he has trained.  He had babesia really bad and was so ill he could barely walk up 5 steps.  He has his life back now with teasel.  He found them just when he was contemplating suicide again (due to the bartonella in the brain).
 
Sandra
----- Original Message -----
From: Tess Gomez
Sent: Monday, November 09, 2009 3:34 PM
Subject: Re: [lymestrategies] no teasel theripist

 

 
I'm about to start the teasel therapy, and the therapist I talked to told me that Babesia which is one of my co-infections, could interfere with the success of this therapy since Babesia is not caused by bacteria but by protozoan, so I'm wondering if I should wait until babesia is out of the picture.
Any comments about this would be appreciated. Thank you.
 
Tess


--- On Mon, 11/9/09, Susan Siegel <ssiegel5@verizon.net> wrote:

From: Susan Siegel <ssiegel5@verizon.net>
Subject: Re: [lymestrategies] no teasel theripist
To: lymestrategies@yahoogroups.com
Date: Monday, November 9, 2009, 8:05 PM

Call my practitioner.  She does distance sessions.  Me, my husband, 
and my daughter have all done this with success.

Trish Mooney
http://www.rockwaterhealing.com/
  (301) 996-5656

Susan

On Nov 9, 2009, at 2:55 PM, bacwannaski wrote:

> non s/c well delta gardens left me a message on my phone and said 
> there is no theripist in my area im waiting to here from sue massie 
> I missed her the first time she called.I am so depresed I feel my 
> lyme is gettinhg worse the  s/c had stoped makeing me improve but I 
> think it was stoping me from getting worse now I can,t take it cause 
> I can,t drink that much water now I hope there is other hope out 
> there for me just unlodeing .Becky
>
>
>
> ------------------------------------
>
> The information anywhere on Lyme Strategies should not be considered 
> complete, nor should it be relied on or interpreted to suggest a 
> course of treatment for any individual.  It is research information 
> only and it should not be used in place of a visit, call, 
> consultation or the advice of your physician or other qualified 
> health care provider.  Information obtained with regards to Lyme 
> Strategies is research only on an ongoing basis for review and 
> evaluation.  Any application or implementation of research 
> information is considered at the members own risk.  The providers of 
> the Lyme Strategies site are not medical physicians.  Should you 
> have any health care-related questions, please call or see your 
> physician or other qualified health care provider promptly. Yahoo! 
> Groups Links
>
>
>



------------------------------------

The information anywhere on Lyme Strategies should not be considered complete, nor should it be relied on or interpreted to suggest a course of treatment for any individual.  It is research information only and it should not be used in place of a visit, call, consultation or the advice of your physician or other qualified health care provider.  Information obtained with regards to Lyme Strategies is research only on an ongoing basis for review and evaluation.  Any application or implementation of research information is considered at the members own risk.  The providers of the Lyme Strategies site are not medical physicians.  Should you have any health care-related questions, please call or see your physician or other qualified health care provider promptly. Yahoo! Groups Links

<*> To visit your group on the web, go to:
    http://groups.yahoo.com/group/lymestrategies/

<*> Your email settings:
    Individual Email | Traditional

<*> To change settings online go to:
    http://groups.yahoo.com/group/lymestrategies/join
    (Yahoo! ID required)

<*> To change settings via email:
    lymestrategies-digest@yahoogroups.com
    lymestrategies-fullfeatured@yahoogroups.com

<*> To unsubscribe from this group, send an email to:
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    http://docs.yahoo.com/info/terms/



Reply | Forward | Messages in this Topic (38)
#87074 From: "Sandra Gikas" <skg59@...>
Date: Mon Nov 9, 2009 9:29 pm
Subject: Re: no teasel theripist 		gikassandra
Offline Offline
Send Email Send Email
 
Did you call the other woman I told you to call?
 
Sandra
----- Original Message -----
Sent: Monday, November 09, 2009 2:55 PM
Subject: [lymestrategies] no teasel theripist

 

non s/c well delta gardens left me a message on my phone and said there is no theripist in my area im waiting to here from sue massie I missed her the first time she called.I am so depresed I feel my lyme is gettinhg worse the s/c had stoped makeing me improve but I think it was stoping me from getting worse now I can,t take it cause I can,t drink that much water now I hope there is other hope out there for me just unlodeing .Becky


Reply | Forward | Messages in this Topic (38)
#87073 From: "harmonyetc" <ekolsen5@...>
Date: Mon Nov 9, 2009 8:44 pm
Subject: Re: non S/C: Colloidal Silver ? 		harmonyetc
Offline Offline
Send Email Send Email
  
Evidently it is very difficult to get in on this tight knit group as I've tried
more than once with little or no response to my questions.

I must not be asking right or something so I'm back to lurking here and
continuing to search for answers elsewhere.  Blessings and healing to everyone
here.  K

--- In lymestrategies@yahoogroups.com, "harmonyetc" <ekolsen5@...> wrote:
>
> I just took my first 2oz of colloidal silver this morning and will take 4 more
oz spread throughout the day.  Aside from having a headache and some dizziness I
have not noticed anything else (thank goodness).
>
> Is this similar to what I can expect from this amount?  I know everyone is
different, but what I'm asking is more... Reaction that is OK ( I can tolerate)
vs. bedridden herxing.
>
> I have an idea of how to support my detox pathways, but does anyone here have
any added suggestions?  I would greatly appreciate the help.
>

Reply | Forward | Messages in this Topic (7)
#87072 From: Tess Gomez <tessmez@...>
Date: Mon Nov 9, 2009 8:34 pm
Subject: Re: no teasel theripist 		tessmez
Offline Offline
Send Email Send Email
 
 
I'm about to start the teasel therapy, and the therapist I talked to told me that Babesia which is one of my co-infections, could interfere with the success of this therapy since Babesia is not caused by bacteria but by protozoan, so I'm wondering if I should wait until babesia is out of the picture.
Any comments about this would be appreciated. Thank you.
 
Tess


--- On Mon, 11/9/09, Susan Siegel <ssiegel5@...> wrote:

From: Susan Siegel <ssiegel5@...>
Subject: Re: [lymestrategies] no teasel theripist
To: lymestrategies@yahoogroups.com
Date: Monday, November 9, 2009, 8:05 PM

Call my practitioner.  She does distance sessions.  Me, my husband, 
and my daughter have all done this with success.

Trish Mooney
http://www.rockwaterhealing.com/
  (301) 996-5656

Susan

On Nov 9, 2009, at 2:55 PM, bacwannaski wrote:

> non s/c well delta gardens left me a message on my phone and said 
> there is no theripist in my area im waiting to here from sue massie 
> I missed her the first time she called.I am so depresed I feel my 
> lyme is gettinhg worse the  s/c had stoped makeing me improve but I 
> think it was stoping me from getting worse now I can,t take it cause 
> I can,t drink that much water now I hope there is other hope out 
> there for me just unlodeing .Becky
>
>
>
> ------------------------------------
>
> The information anywhere on Lyme Strategies should not be considered 
> complete, nor should it be relied on or interpreted to suggest a 
> course of treatment for any individual.  It is research information 
> only and it should not be used in place of a visit, call, 
> consultation or the advice of your physician or other qualified 
> health care provider.  Information obtained with regards to Lyme 
> Strategies is research only on an ongoing basis for review and 
> evaluation.  Any application or implementation of research 
> information is considered at the members own risk.  The providers of 
> the Lyme Strategies site are not medical physicians.  Should you 
> have any health care-related questions, please call or see your 
> physician or other qualified health care provider promptly. Yahoo! 
> Groups Links
>
>
>



------------------------------------

The information anywhere on Lyme Strategies should not be considered complete, nor should it be relied on or interpreted to suggest a course of treatment for any individual.  It is research information only and it should not be used in place of a visit, call, consultation or the advice of your physician or other qualified health care provider.  Information obtained with regards to Lyme Strategies is research only on an ongoing basis for review and evaluation.  Any application or implementation of research information is considered at the members own risk.  The providers of the Lyme Strategies site are not medical physicians.  Should you have any health care-related questions, please call or see your physician or other qualified health care provider promptly. Yahoo! Groups Links

<*> To visit your group on the web, go to:
    http://groups.yahoo.com/group/lymestrategies/

<*> Your email settings:
    Individual Email | Traditional

<*> To change settings online go to:
    http://groups.yahoo.com/group/lymestrategies/join
    (Yahoo! ID required)

<*> To change settings via email:
    lymestrategies-digest@yahoogroups.com
    lymestrategies-fullfeatured@yahoogroups.com

<*> To unsubscribe from this group, send an email to:
    lymestrategies-unsubscribe@yahoogroups.com

<*> Your use of Yahoo! Groups is subject to:
    http://docs.yahoo.com/info/terms/



Reply | Forward | Messages in this Topic (38)
#87071 From: Susan Siegel <ssiegel5@...>
Date: Mon Nov 9, 2009 8:05 pm
Subject: Re: no teasel theripist 		ssiegel921
Offline Offline
Send Email Send Email
  
Call my practitioner.  She does distance sessions.  Me, my husband,
and my daughter have all done this with success.

Trish Mooney
http://www.rockwaterhealing.com/
   (301) 996-5656

Susan

On Nov 9, 2009, at 2:55 PM, bacwannaski wrote:

> non s/c well delta gardens left me a message on my phone and said
> there is no theripist in my area im waiting to here from sue massie
> I missed her the first time she called.I am so depresed I feel my
> lyme is gettinhg worse the  s/c had stoped makeing me improve but I
> think it was stoping me from getting worse now I can,t take it cause
> I can,t drink that much water now I hope there is other hope out
> there for me just unlodeing .Becky
>
>
>
> ------------------------------------
>
> The information anywhere on Lyme Strategies should not be considered
> complete, nor should it be relied on or interpreted to suggest a
> course of treatment for any individual.  It is research information
> only and it should not be used in place of a visit, call,
> consultation or the advice of your physician or other qualified
> health care provider.  Information obtained with regards to Lyme
> Strategies is research only on an ongoing basis for review and
> evaluation.  Any application or implementation of research
> information is considered at the members own risk.  The providers of
> the Lyme Strategies site are not medical physicians.  Should you
> have any health care-related questions, please call or see your
> physician or other qualified health care provider promptly. Yahoo!
> Groups Links
>
>
>

Reply | Forward | Messages in this Topic (38)
#87070 From: "Nancy Wilson" <wilson33@...>
Date: Mon Nov 9, 2009 7:58 pm
Subject: RE: no teasel theripist 		zoie19582002
Offline Offline
Send Email Send Email
 
Hang in there Becky - are you doing Cat's claw or Salt/C or both? I have been doing both for over a year and some days are just better than others.
 
Seems like the more you kill the worse you feel so take everything slow and make your health your biggest priority!
 
Nancy

From: lymestrategies@yahoogroups.com [mailto:lymestrategies@yahoogroups.com] On Behalf Of bacwannaski
Sent: Monday, November 09, 2009 11:56 AM
To: lymestrategies@yahoogroups.com
Subject: [lymestrategies] no teasel theripist

 

non s/c well delta gardens left me a message on my phone and said there is no theripist in my area im waiting to here from sue massie I missed her the first time she called.I am so depresed I feel my lyme is gettinhg worse the s/c had stoped makeing me improve but I think it was stoping me from getting worse now I can,t take it cause I can,t drink that much water now I hope there is other hope out there for me just unlodeing .Becky


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#87069 From: "bacwannaski" <bacwannaski@...>
Date: Mon Nov 9, 2009 7:55 pm
Subject: no teasel theripist 		bacwannaski
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non s/c well delta gardens left me a message on my phone and said there is no
theripist in my area im waiting to here from sue massie I missed her the first
time she called.I am so depresed I feel my lyme is gettinhg worse the  s/c had
stoped makeing me improve but I think it was stoping me from getting worse now I
can,t take it cause I can,t drink that much water now I hope there is other hope
out there for me just unlodeing .Becky

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#87068 From: "Cindi Callanan" <cindicallanan@...>
Date: Mon Nov 9, 2009 6:58 pm
Subject: Re: non salt/c coconut oil 		cindi_callanan
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Sometimes... it's an antifungal, antibacterial, and a thermogenic oil, so it builds adrenal and thyroid energy, which also allows for detox and herx.
 
Cindi Callanan, MsT, CST, BEC
Power Wellness Solutions
Integrative Wellness Consultant/Health Coach
National Cleansing Coach
410-771-4994 O
443-980-7369 Cell
----- Original Message -----
Sent: Monday, November 09, 2009 10:58 AM
Subject: [lymestrategies] non salt/c coconut oil

 

Can coconut oil cause herxing?
 
Sandra


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#87067 From: "baker_horace" <baker_horace@...>
Date: Mon Nov 9, 2009 6:54 pm
Subject: Re: non salt/c coconut oil 		baker_horace
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I herx from coconut oil, but it's pretty much confined to the gut.

--- In lymestrategies@yahoogroups.com, "Sandra Gikas" <skg59@...> wrote:
>
> Can coconut oil cause herxing?
>
> Sandra
>

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#87066 From: Susan Siegel <ssiegel5@...>
Date: Mon Nov 9, 2009 6:33 pm
Subject: Re: non salt/c coconut oil 		ssiegel921
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Perhaps from yeast, but not lyme or coinfections.


On Nov 9, 2009, at 10:58 AM, Sandra Gikas wrote:



Can coconut oil cause herxing?
 
Sandra




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#87065 From: Kendra <KCuyler@...>
Date: Mon Nov 9, 2009 6:09 pm
Subject: Re: high blood pressure 		suzyq46360
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Hello
 
You don't mention what kind of salt and what kind of vitamin C.  There are many different types, some better than others, i.e. sea salt (Celtic, Himalyan... vs. Morton's -common table salt) and vit C that includes the full complex of bioflavinoids. 
 
I know that some people are using a newer product instead of C (I think) called apple polyphenols?
 
Did you ramp up slowly, per the group guidelines?  Was your blood pressure also high at lower doses of Salt/C? 
 
Except for the high blood pressure, have you noticed symptom relief from the Salt/C?
 
Kendra

On Mon, Nov 9, 2009 at 11:07 AM, homedinger <jackdotcom@...> wrote:
 

Been on Salt/C for three months, daily have taken over that period about 18 grams of each, salt and vitamin C.

Blood pressure remains extremely high, and I had normal before starting this. It is so bad I couldn't sleep the last few nights, so am stopping the salt today for a rest to see what happens. Blood pressure is dangerously high.

I know some have said it will go down after a time, but mine is not going down and I am elderly and in danger from it.


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#87064 From: "homedinger" <jackdotcom@...>
Date: Mon Nov 9, 2009 5:07 pm
Subject: high blood pressure 		homedinger
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Been on Salt/C for three months, daily have taken over that period about 18
grams of each, salt and vitamin C.

Blood pressure remains extremely high, and I had normal before starting this. 
It is so bad I couldn't sleep the last few nights, so am stopping the salt today
for a rest to see what happens.  Blood pressure is dangerously high.

I know some have said it will go down after a time, but mine is not going down
and I am elderly and in danger from it.

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#87063 From: "Sandra Gikas" <skg59@...>
Date: Mon Nov 9, 2009 3:58 pm
Subject: non salt/c coconut oil 		gikassandra
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Can coconut oil cause herxing?
 
Sandra

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#87062 From: "Sandra Gikas" <skg59@...>
Date: Mon Nov 9, 2009 3:58 pm
Subject: Re: OT: does modifilan bind toxins in general, or just heavy metals? 		gikassandra
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It binds toxins too;
 
Sandra
----- Original Message -----
From: svg32000
Sent: Monday, November 09, 2009 9:43 AM
Subject: [lymestrategies] OT: does modifilan bind toxins in general, or just heavy metals?

 




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#87061 From: "Scott Adams" <msadams@...>
Date: Mon Nov 9, 2009 3:07 pm
Subject: free Lyme Resource CD 		msadams
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I send this out every 2 weeks for new folks who might not have seen it. Sorry to spam but its the easiest way I know to let newcomers hear about it.
 
I have a free Lyme Resource CD available at:
 
 
This was last sent 10/08/09
 
Scott Adams
 

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#87060 From: "svg32000" <svg32000@...>
Date: Mon Nov 9, 2009 2:43 pm
Subject: OT: does modifilan bind toxins in general, or just heavy metals? 		svg32000
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#87059 From: Kendra <KCuyler@...>
Date: Mon Nov 9, 2009 7:22 am
Subject: Re: Re: Far Infrared Sauna 		suzyq46360
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Dear Amanda
 
How will be get far-infrared heat/waves withOUT a heater?  Just closing yourself up in a sleeping bag type unit will not produce infrared heat in any way that I can imagine.... 
 
Though, I guess there are some heating pad type things (Bio-mats?) that produce far-infrared (sp?) without using a ceramic heater type unit.  Is that the distinction you are trying to make?
Do any of the sellers offer a satisfaction or money-back guarantee?  Do they all have excellent feedback?
 
Good luck -- please let us know which one you decide on and how it works after you get it. 
 
Warmest regards,
Kendra
On Sun, Nov 8, 2009 at 9:32 PM, amandaleehancock <amandalynnlee@...> wrote:
Hi,

I am about to buy a portable infrared sauna. It sounds like most people have positive feedback and it has helped make them feel better. I need a lot of help detoxing. My LLMD did some genetic testing that revealed I have some abnormalities in my liver enzymes that impact my ability to detox.

I'm wondering if anyone thinks there is any negative impact to using a portable infrared sauna?

Also, if anyone has information to share such as how long you stay in, how many days a week, and at what temperature, that would be great. I want to be sure I'm getting the most out of it, and safely.

It sounds like this detoxing has helped people with herxes, but I'm wondering if it has caused anyone to herx?

Also, I'm curious as to who's using it with a heater or without? Some are selling without, saying the carbon panels heat it up. My impression is that a heater just helps it heat up more quickly. But, I'm not sure I'm right?
<snip>
Amanda


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