Poison cures life..

From your head down to your feet.

      In unconventional warfare, manipulated beliefs are used to displace
inconvenient facts. When waging war by way of deception, false beliefs are a
weapon.

      The Main Human Mycoplasma Pathogens

      Chronic pelvic inflammatory disease,  infertility, Gulf War Syndrome,
Fibromyalgia, Chronic Fatigue Syndrome, Lupus, AIDS/HIV, ALS, psoriasis and
Scleroderma, Crohn's and IBS, Lyme disease, cancer, endocrine disorders,
Multiple Sclerosis, diabetes, TMJ disorders, Eye and ear disorders and
infections, gingivitis, periodontal diseases including cavities, infertility,
urethritis, vaginitis, cervicitis, amnionitis, pyelonephritis, post-partum
septicemia, neonatal pneumonia, neonatal conjunctivitis, Reiter's syndrome,
peritonitis, wound infections , low birth weight infants,  mycoplasma pneumonia,
pneumonia, asthma, upper and lower respiratory diseases, heart diseases,
leukemia, Steven-Johnson syndrome, septic arthritis, CNS disorders and diseases,
urinary tract infections, Crohn's and Irritable Bowel Syndrome, Guillain-Barr
syndrome, polyradiculitis, encephalitis, and septic meningitis, autoimmune
diseases, mycoplasma incognitus, urogenital infections and diseases.

         The mycoplasma enters the individual cells of the body and may develop
neurological diseases if the pathogen destroys certain cells in your brain, or
you may develop Crohn's colitis if the pathogen invades and destroys cells in
the lower bowel. Once it gets into the cell, it can lie there doing nothing
sometimes for 10 or 30 years, but if a trauma occurs like an accident, or
vaccination, the mycoplasma can become triggered.

          Deceit is not new to warfare. What's new is the reach. They don't want
the smoking gun to be a mushroom cloud. Eugenics is now known as epigenetics, to
be politically-correct, a world turned inside out where the victim is cast as
aggressor and the predator as prey.


      Ouroboros

---

From: lymestrategies@yahoogroups.com [mailto:lymestrategies@yahoogroups.com] On Behalf Of Jim in Jax
Sent: Tuesday, November 10, 2009 4:34 PM
To: LymeStrategies Group; Lyme and Rife Group thane
Subject: [lymestrategies] Heart issues - much worse

Hey everyone,

My heart issues worsened greatly this past Friday and today I am not doing well at all... On the advice of my ER doctor friend who's been kind enough to guide me these past few days, I am heading back to the ER right now....

Take care everyone,

Jim

Thank you all for replying.  I have only gotten up to 4 oz so far as I've been
experiencing severe dizziness.  Last check my borrelia counts are down but I'm
sure I have other microorgs.  It was in reducing my mercury load that activated
the dormant Lyme in the first place. K


--- In lymestrategies@yahoogroups.com, "mercurybeater" <mercurybeater@...>
wrote:
>
> 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.
> > >
> >
>

--- In lymestrategies@yahoogroups.com, Jim in Jax <jimjax2@...> wrote:
>
> Hey everyone,
>
> My heart issues worsened greatly this past Friday and today I am not doing
> well at all... On the advice of my ER doctor friend who's been kind enough
> to guide me these past few days, I am heading back to the ER right now....
>
> Take care everyone,
>
> Jim
>
My thoughts and prayers are with you my friend. Please keep us posted.

----- Original Message -----

From: Jim in Jax

To: LymeStrategies Group ; Lyme and Rife Group thane

Sent: Tuesday, November 10, 2009 5:34 PM

Subject: [lymestrategies] Heart issues - much worse

 

Hey everyone,

My heart issues worsened greatly this past Friday and today I am not doing well at all... On the advice of my ER doctor friend who's been kind enough to guide me these past few days, I am heading back to the ER right now....

Take care everyone,

Jim

Hi,

I am the most typical, chronic, severe case of fibromyalgia. I found out that I
have Lyme over a year ago. I think there are other things that can contribute to
a state of FMS, but I know a lot of people with FMS have found out they have
Lyme.

As far as tryptophan, I took it once for a protocol to help with sleep. This
could help someone. It did nothing for me. My LLMD has a protocol in which he
uses tryptophan.

As well, he recommends the Ribose mixed in water, to help energy for people with
fatigue. I tried it in his office, and then I slept for 4 hard hours!! So
unfortunately it didn't work for me. But, it seems it can be helpful.

So, I think these things are Lyme specific, and some of us are Fibro Lymies. In
Lyme, our ability to produce ATP can be affected, and so I think there
definitely is a clear connection to FMS. We don't have energy- it has to start
somewhere.

Amanda




--- In lymestrategies@yahoogroups.com, Susan Siegel <ssiegel5@...> wrote:
>
> I second this!  Whenever there is an ache or pain in our house, we get
> out the DMSO cream and slather it on.
> Susan
>
> On Nov 9, 2009, at 8:43 PM, haecklers wrote:
>
> > 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
> >>>
> >>
> >
> >
> >
> >
> > ------------------------------------
> >
> > 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
> >
> >
> >
>

Hi Jim,

I am so sorry about your heart issues.  Rest assured, I will be praying for you.
Father God, I ask you now to surround Jim with the white light so evil cannot
get to him.  Father, You are our healer and I ask you to heal Jim from the top
of his head to the bottom of his feet, now in the name of Jesus.  Amen

Jim, keep us posted as you can.  You are very important to all of us.

Love,
Mona

--- In lymestrategies@yahoogroups.com, Jim in Jax <jimjax2@...> wrote:
>
> Hey everyone,
>
> My heart issues worsened greatly this past Friday and today I am not doing
> well at all... On the advice of my ER doctor friend who's been kind enough
> to guide me these past few days, I am heading back to the ER right now....
>
> Take care everyone,
>
> Jim
>

So sorry to hear it.  Best wishes for a speedy turnaround.

Phil L.


--- In lymestrategies@yahoogroups.com, Jim in Jax <jimjax2@...> wrote:
>
> Hey everyone,
>
> My heart issues worsened greatly this past Friday and today I am not doing
> well at all... On the advice of my ER doctor friend who's been kind enough
> to guide me these past few days, I am heading back to the ER right now....
>
> Take care everyone,
>
> Jim
>

----- Original Message -----

From: Sandra Gikas

To: lymestrategies@yahoogroups.com

Sent: Tuesday, November 10, 2009 2:48 PM

Subject: [SPAM] Re: [lymestrategies] Re: Non S/C:Desperate Coconut oil for Inflammation?, Type of Iodine for Thyroid?

 

Cat's Claw by Raintree Nutrition is a very good anti-inflammatory and also boosts the immune system.

 

Sandra

----- Original Message -----

From: lymegal2008

To: lymestrategies@yahoogroups.com

Sent: Monday, November 09, 2009 7:53 PM

Subject: [lymestrategies] Re: Non S/C:Desperate Coconut oil for Inflammation?, Type of Iodine for Thyroid?

 

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
>

----- Original Message -----

From: RRM

To: lymestrategies@yahoogroups.com

Sent: Tuesday, November 10, 2009 12:34 PM

Subject: [lymestrategies] susan-no teasel theripist

 

energetic? do you mean someone/thing sent you the frequency of teasel root?remotly roger --- On Tue, 11/10/09, Susan Siegel <ssiegel5@verizon.net> wrote: From: Susan Siegel <ssiegel5@verizon.net> Subject: Re: [lymestrategies] susan-no teasel theripist To: lymestrategies@yahoogroups.com Date: Tuesday, November 10, 2009, 6:53 AM   This last flare up (reinfection? ) I used primarily the energetic teasel treatments and some artisimin (?). Susan  On Nov 10, 2009, at 4:53 AM, RRM wrote: what did you use for babesia? just teasel root? roger --- 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, 6:32 PM 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.rockwate rhealing. 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/lymestrate gies/ <*> Your email settings:     Individual Email | Traditional <*> To change settings online go to:     http://groups. yahoo.com/ group/lymestrate gies/join     (Yahoo! ID required) <*> To change settings via email:     lymestrategies- digest@yahoogrou ps.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/

----- Original Message -----

From: RRM

To: lymestrategies@yahoogroups.com

Sent: Tuesday, November 10, 2009 4:53 AM

Subject: [lymestrategies] susan-no teasel theripist

 

what did you use for babesia? just teasel root? roger --- 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, 6:32 PM   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.rockwate rhealing. 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/lymestrate gies/ <*> Your email settings:     Individual Email | Traditional <*> To change settings online go to:     http://groups. yahoo.com/ group/lymestrate gies/join     (Yahoo! ID required) <*> To change settings via email:     lymestrategies- digest@yahoogrou ps.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/

----- Original Message -----

From: lymegal2008

To: lymestrategies@yahoogroups.com

Sent: Monday, November 09, 2009 7:53 PM

Subject: [lymestrategies] Re: Non S/C:Desperate Coconut oil for Inflammation?, Type of Iodine for Thyroid?

 

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
>

----- Original Message -----

From: Susan Siegel

To: lymestrategies@yahoogroups.com

Sent: Tuesday, November 10, 2009 3:08 PM

Subject: Re: [lymestrategies] susan- teasel therapy

 

Yes.  Practitioners are trained by Delta Gardens and use the flowers essences of the teasel plant to relieve symptoms of lyme disease and its coinfections.  I found a practitioner in my area (because of a nasty reinfection of babesia courtesy of my husband) and it has been very successful for me (and my husband and daughter).  Many practitioners also offer distance treatments.

www.deltagardens.com

On Nov 10, 2009, at 12:34 PM, RRM wrote:

energetic? do you mean someone/thing sent you the frequency of teasel root?remotly roger --- On Tue, 11/10/09, Susan Siegel <ssiegel5@verizon.net> wrote:

Hi Everyone!
I was hoping someone has tried "prill water" and would share their thoughts &
experience with me. If it does indeed increase the absorbtion of water into the
body, I would think that it would be a valuable mechanism for us Lymies to take
advantage of. Thanks for sharing any info you can.
Be Well!
Linda