LymeOz : Messages : 1147-1176 of 1176

Hi Karin,

I am so glad you had a good get together. I don’t know Aimee very well, but she seems really nice and open to suggestions on how to get well. I have known Phil for years over the internet and phone. He is an awesome guy who is a great encouragement to others. He is very generous and will go to great lengths to help others get well. I love knowing that the Lyme community is reaching out to help each other. That is fantastic.

Hang in there,

Rosemary.

From: LymeOz@... [mailto:LymeOz@...] On Behalf Of Karin Floate
Sent: Saturday, 26 December 2009 7:10 PM
To: LymeOz@...
Subject: Re: [LymeOz]Cholestrymaine

Was great to meet Phil and Aimee today. I now have more trust in the s/c protocol, and will certainly continue, just wish it would work a bit faster.

Karin

#1175

From: Karin Floate <karinfloate@...>
Date: Sat Dec 26, 2009 8:09 am
Subject:: Re: Cholestrymaine

karinfloate

Offline

Was great to meet Phil and Aimee today. I now have more trust in the s/c protocol, and will certainly continue, just wish it would work a bit faster.

Karin

From: Vic & Rosemary <rosy1@...>
To: Karin Floate <karinfloate@...>
Sent: Sat, 26 December, 2009 11:49:57 AM
Subject: RE: [LymeOz]Cholestrymaine

Hi Karin,

I hope you have a great day with Phil and Aime.

God bless,

Rosemary.

From: Karin Floate [mailto:karinfloate@...]
Sent: Thursday, 24 December 2009 6:13 PM
To: rosy1@...
Subject: Re: [LymeOz]Cholestrymaine

Hi Rosemary

You really know exactly, what it is like to keep going day after day,bit better and then worse again. this time of the year,just does seem really bad. Phil is visiting us on boxingday, and Amie [Lyme oz] will be here, too. I am nervous but exited to meet them. I think, that it will give me a boost, because Phil was like you, also sick for a long time, and he is really well now. Thank you for your kind words. I have a script
for Cholestrymaine, so I can try that for a while. Hope next year will be better for all of us.

lots of love

Karin

From: Vic & Rosemary < rosy1@... >
To: Karin Floate <karinfloate@...>
Sent: Thu, 24 December, 2009 2:20:20 PM
Subject: RE: [LymeOz]Cholestrymaine

Hi Karin,

I am really sorry that you are having a bad day. Lyme can cause depression and anxiety, but there are also so many losses along the way with any chronic illness. Christmas is hard as we see people going out and enjoying things which we can’t do. It really is a tough time for so many people who are in grief because of illness, divorce, unemployment, death of loved ones, etc. Your feelings are completely normal.

As you gradually get well you will find that your dark times are not so often or so deep and you will have more good times.

I have had a really tough year, but thanks to salt & C I have been well enough to cope and even enjoy my life again.

Hang in there and just keep going forward, one step at a time,

Rosemary.

From: Karin Floate [mailto:karinfloate@...]
Sent: Wednesday, 23 December 2009 4:07 PM
To: Vic & Rosemary
Subject: Re: [LymeOz]Cholestrymaine

Hi Rosemary

Thank you for your advice and concern. I have asked my dr. for a script. I am having a really awful day, cant stop the tears and the depression and symptons are overwhelming. I is not like that all the time, I have much better days in between, when I can drive my car, and go to the shops, if some one is with me. I am on antidepressant, it does help with sleeping..

lots of love Karin

From: Vic & Rosemary < rosy1@... >
To: LymeOz@...
Sent: Wed, 23 December, 2009 2:38:09 PM
Subject: RE: [LymeOz]Cholestrymaine

Hi Karin,

A lot of our symptoms can be die-off as the bugs are killed and they emit nasty toxins. Cholestyramine definitely helps many people to get rid of the toxins. I think it is worth trying in your case. Ask your doctor to prescribe it. It is low risk, has been around for years and not difficult to add to your treatment plan. It just requires mixing up a sachet of white powder in water and drinking it. You just have to make sure you don’t get constipated as this can cause bowel obstruction. Have plenty of fluids, fruit and veggies and you should be fine. You will soon know if it is helping. Keep killing the bugs.

Rosemary.

From: LymeOz@yahoogroups. com.au [mailto: LymeOz@yahoogroups. com.au ] On Behalf Of Karin Floate
Sent: Wednesday, 23 December 2009 12:55 PM
To: LymeOz@yahoogroups. com.au
Subject: Re: [LymeOz]Cholestryma ine

Hi Nat.

Thankyou for your advise about cholestrrymine. Muscle and nerve pain are not my Symptons. I have bad brain fog. low energie headache and tremors, and feeling awful a lot of the time+ depression. I don't know if it would help. Thank you any way.

x Karin

From: "natalieyoung@ y7mail.com" <natalieyoung@ y7mail.com>
To: LymeOz@yahoogroups. com.au
Sent: Wed, 16 December, 2009 6:29:30 PM
Subject: Re: [LymeOz]Cholestryma ine

Hi Karin the cholestrymaine has helped with my pain thats for sure after 10 months of severe pain 8-10/10 everyday in just 7 weeks it has reduced to just 4/10 somedays less it hasnt however helped with muscle twitching and sore burning throat and abdomen spasms so my breathing is still crap and i am still fatigued however slightly less somewhat.

if you have etreme muscle and nerve pain give it a try its worth a bit of relief

nat young

--- In LymeOz@yahoogroups. com.au, Karin Floate <karinfloate@ ...> wrote:
>
> Â Hi everyone.
>
> Â I have been reading about Cholestyramine.Â Does it help with detox.?Â Does some one know more about it?
>
>
> thanks
> Karin
>
>
> ____________ _________ _________ __
> From: Karin Floate <karinfloate@ ...>
> To: LymeOz@yahoogroups. com.au
> Sent: Mon, 7 December, 2009 1:34:47 PM
> Subject: [LymeOz] hello aimee
>
> Â
> Â HiÂ Aimee
>
> Â Thank you for your e-mail. I am having a bad day to day, so glad that you have answered, some times the most comfort is from fellow sufferers. Have you been ill long, and can I ask where you live. I live inSydney, and removed a tick from Â my headÂ in September 2008, while spending a few days in QLD.Â Are you on more than 1 ABX?? How does one get through the day.??
>
> Â Kind regards
> Â Karin
>
>
>
>
> ____________ _________ _________ __
> From: usalymegirl <summersa@hotmail. com>
> To: LymeOz@yahoogroups. com.au
> Sent: Mon, 7 December, 2009 12:59:51 PM
> Subject: [LymeOz] Rosemary - Re: why is life so hard?
>
> Â
> Hi Karin,
>
> I am new to LymeOz so we haven't spoken before. Your post really resonated with me, because I am struggling with staying positive as well. It is hard to see how far I have come in the past year.
>
> When you are living daily with pain, fatigue, brain fog it is only natural to lose perspective. That's why I like to check in with others to see what they have observed.
>
> I have been on abx for 12 months now and I have made progress. I am coming to the end of my first tx regimen and I am thinking about taking a break from the abx and trying the Salt/C protocol. I also have a rife machine and have been using that for 1 month.
>
> I want to wait until I am off abx to start the salt/c, that way I will know if the salt/c is working and won't get my progress confused with the abx.
>
> Hang in there and never, never give up!
> Aimee
>
> --- In LymeOz@yahoogroups. com.au, Karin Floate <karinfloate@ ...> wrote:
> >
> > Ã‚Â HiÃ‚Â Aimee
> > Ã‚Â We have not spocken before. Are you doing the s/c protocol, and how long. Thank's for the kind words.
> >
> > Karin
> >
> >
> >
> >
> > ____________ _________ _________ __
> > From: usalymegirl <summersa@ .>
> > To: LymeOz@yahoogroups. com.au
> > Sent: Thu, 3 December, 2009 7:51:28 PM
> > Subject: [LymeOz] Rosemary - Re: why is life so hard?
> >
> > Ã‚Â
> > Karin,
> >
> > From personal experience I think it is hard to see our own progress b/c we live with this disease everyday. It is hard to be objective.
> >
> > The fact that your family has noticed changes and that you are driving again is HUGE - congrats.
> >
> > Maybe once a month you can check in with friends and family and ask their opinions on how you are doing. And ask how you are doing in relation to the previous month. That way when/if you have a bad day and get fustrated, you can remember that family and friends have noticed improvements.
> >
> > Aimee
> >
> > --- In LymeOz@yahoogroups. com.au, "Vic & Rosemary " <rosy1@> wrote:
> > >
> > > Hi Karin,
> > >
> > > I am so thrilled you can drive again. This is a huge step forward. Driving
> > > requires a lot of neurological functions.
> > >
> > > Best regards,
> > >
> > > Rosemary .
> > >
> > >
> > >
> > > _____
> > >
> > > From: LymeOz@yahoogroups. com.au [mailto:LymeOz@ yahoogroups. com.au] On Behalf
> > > Of Karin Floate
> > > Sent: Wednesday, 2 December 2009 10:51 AM
> > > To: LymeOz@yahoogroups. com.au
> > > Subject: Re: [LymeOz] Rosemary - Re: why is life so hard?
> > >
> > >
> > >
> > >
> > >
> > > Hi Leonnie
> > >
> > >
> > >
> > > How are you going with the s/c? Are you getting to the higher doses? My
> > > family and friends can see im provements, but I have trouble seeing it. But
> > > I can drive my car again, which I have not been able to do for 1 year. We
> > > really must have patience , and be percistent.
> > >
> > >
> > >
> > > Karin
> > >
> >
> >
> >
> >
> >
> > ____________ _________ _________ _________ _________ _________ _
> > Win 1 of 4 Sony home entertainment packs thanks to Yahoo!7.
> > Enter now: http://au.docs. yahoo.com/ homepageset/
> >
>
>
> ____________ _________ _________ __
> See what's on at the movies in your area. Find out now.
>
>
>
> ____________ _________ _________ _________ _________ _________ _
> See what's on at the movies in your area. Find out now: http://au.movies. yahoo.com/ session-times/
>

See what's on at the movies in your area. Find out now.

#1174

From: "Vic & Rosemary" <rosy1@...>
Date: Fri Dec 25, 2009 11:52 pm
Subject:: RE: A very special Christmas wish :-)

aussietickchick

Offline

Hi Phil,

Thanks to your encouragement Vic and I have ramped right up to 10-12 doses. We are certainly kicking spirochete butt and look forward to many more gains in the coming year.

May you all enjoy the many wonderful improvements that we have experienced.

Best regards,

Rosemary.

From: LymeOz@... [mailto:LymeOz@...] On Behalf Of Phil Rich
Sent: Thursday, 24 December 2009 8:14 PM
To: LymeOz@...
Subject: [LymeOz] A very special Christmas wish :-)

I would like to wish everyone a wonderful christmas … and the BEST… and the MOST HEALTHY new year ahead - let's kick some spirochete butt!!!

Regards,

Phil Rich

#1173

From: "Phil Rich" <philrich@...>
Date: Thu Dec 24, 2009 9:13 am
Subject:: A very special Christmas wish :-)

philcr2004

Offline

I would like to wish everyone a wonderful christmas … and the BEST… and the MOST HEALTHY new year ahead - let's kick some spirochete butt!!!

Regards,

Phil Rich

#1172

From: Karin Floate <karinfloate@...>
Date: Wed Dec 23, 2009 5:12 am
Subject:: Re: PDT for cancer update. (off topic)

karinfloate

Offline

Good that Vic and you are doing well. Very sad to hear about Amy .She was to young to pass away.

x Karin

From: Vic & Rosemary <rosy1@...>
To: LymeOz@...
Sent: Wed, 23 December, 2009 2:46:41 PM
Subject: [LymeOz] PDT for cancer update. (off topic)

Hi Gang,

You may recall that Vic had PDT treatment for his prostate cancer back in September/0ctober. We still have to wait for a specialist appointment in the New Year to see if the cancer is all gone. However, his color remains so much better and he is doing quite well. I will keep you posted when we know for sure what the tests reveal.

Meanwhile we have increased our doses of salt & C and are both doing very well.

On a sadder note, young Amy, the woman with tongue cancer passed away 3 days ago. She had been doing so well with the cancer receding, gaining weight, etc. But eventually the cancer began growing faster than the PDT could kill it. We had witnessed her huge improvements and had great hopes for her recovery, but it wasn’t meant to be, as she was in the last stages of the cancer.

She leaves behind a beautiful 11 month old baby girl. Our hearts go out to her family.

Rosemary.

See what's on at the movies in your area. Find out now.

#1171

From: "Vic & Rosemary" <rosy1@...>
Date: Wed Dec 23, 2009 4:27 am
Subject:: T'was the Night Before Christmas.

aussietickchick

Offline

HI Gang,
This was written by Eric from my old Lyme-Rife group. I think it's fantastic.
Merry Christmas to all,
Rosemary.

'Twas The Night Before Christmas, when all through the house
Not a creature was stirring, not even a tick-bearing mouse.

The stockings were hung by the chimney with care,
In hopes that costly supplements soon would be there.

The spiros weren't nestled all snug in their cysts,
Because I had just rifed, and now they were pissed.

And mamma in her 'kerchief, and I in my socks,
Had just settled down for a night of detox.

When inside my chest there arose such a clatter,
I sprang from my chair won'dring what was the matter.

Away to the laptop I flew like a flash,
Logged into Yahoo and an email I dashed.

The rife group is blessed with intelligent Lymies,
Surely they'll have an answer when I'm just plain stymied.

When, what to my wondering eyes should appear,
But a host of replies, and all full of good cheer.

More rapid than eagles the replies they came,
And I whistled, and shouted, and called them by name:

"There's Skyking, and Firefox, Rob Allen and V!
Ken Uzzell, Carol Yen, and even Sue Massie!"

"In the bite of a herx, toxins will be your fall!
Now flush away! flush away! flush away all!

Heart palpitations sound like your main symptom,
Drink lots of water with lemon to rid them.

In fact, any means of detox will do,
Ozone, FIR sauna, and liver flushes, too!"

And then, in a twinkling, my mind was at ease,
For I had many allies against Lyme Disease.

* * *

Our Lyme Disease symptoms, in time, will be less,
And at this time of year, we all should feel blessed.

We all know the symptoms, though sometimes they vary,
And how they all keep us from being more merry.

But with the help of this group, through error and trial,
We've all found some relief, sought after long whiles.

It's still a long road, but one we must travel,
As we deal with the Lyme, and the lives it has unraveled.

But please don't lose hope, for so many options abound,
In our struggle to fight and regain lost ground.

Rifing, ozone, FIR sauna, magpulsing,
Salt/vitamin C, and Marshal Protocol-ing.

All are more options for Lymies to try,
Not all may work for you, some are costly to buy.

But this struggle is worth it, you'll learn more `bout yourself,
And a wealth of information to improve your health.

So let me just say, as we struggle through our plight,
"Merry Christmas, my friends...keep up the good fight!"

Eric

Reply | Forward | Messages in this Topic (1)

#1170

From: "Vic & Rosemary" <rosy1@...>
Date: Wed Dec 23, 2009 3:46 am
Subject:: PDT for cancer update. (off topic)

aussietickchick

Offline

Hi Gang,

Meanwhile we have increased our doses of salt & C and are both doing very well.

She leaves behind a beautiful 11 month old baby girl. Our hearts go out to her family.

Rosemary.

#1169

From: "Vic & Rosemary" <rosy1@...>
Date: Wed Dec 23, 2009 3:38 am
Subject:: RE: Cholestrymaine

aussietickchick

Offline

Hi Karin,

A lot of our symptoms can be die-off as the bugs are killed and they emit nasty toxins.� Cholestyramine definitely helps many people to get rid of the toxins.� I think it is worth trying in your case.� Ask your doctor to prescribe it.� It is low risk, has been around for years and not difficult to add to your treatment plan.� It just requires mixing up a sachet of white powder in water and drinking it.� You just have to make sure you don’t get constipated as this can cause bowel obstruction.� Have plenty of fluids, fruit and veggies and you should be fine.� You will soon know if it is helping.� Keep killing the bugs.

Rosemary.

From: LymeOz@... [mailto:LymeOz@...] On Behalf Of Karin Floate
Sent: Wednesday, 23 December 2009 12:55 PM
To: LymeOz@...
Subject: Re: [LymeOz]Cholestrymaine

Hi Nat.

x Karin

From: "natalieyoung@y7mail.com" <natalieyoung@y7mail.com>
To: LymeOz@yahoogroups.com.au
Sent: Wed, 16 December, 2009 6:29:30 PM
Subject: Re: [LymeOz]Cholestrymaine

Hi Karin the cholestrymaine has helped with my pain thats for sure after 10 months of severe pain 8-10/10 everyday in just 7 weeks it has reduced to just 4/10 somedays less it hasnt however helped with muscle twitching and sore burning throat and abdomen spasms so my breathing is still crap and i am still fatigued however slightly less somewhat.

if you have etreme muscle and nerve pain give it a try its worth a bit of relief

nat young

--- In LymeOz@yahoogroups. com.au, Karin Floate <karinfloate@ ...> wrote:
>
> � Hi everyone.
>
> � I have been reading about Cholestyramine.� Does it help with detox.?� Does some one know more about it?
>
>
> thanks
> Karin
>
>
> ____________ _________ _________ __
> From: Karin Floate <karinfloate@ ...>
> To: LymeOz@yahoogroups. com.au
> Sent: Mon, 7 December, 2009 1:34:47 PM
> Subject: [LymeOz] hello aimee
>
> �
> � Hi� Aimee
>
> � Thank you for your e-mail. I am having a bad day to day, so glad that you have answered, some times the most comfort is from fellow sufferers. Have you been ill long, and can I ask where you live. I live inSydney, and removed a tick from � my head� in September 2008, while spending a few days in QLD.� Are you on more than 1 ABX?? How does one get through the day.??
>
> � Kind regards
> � Karin
>
>
>
>
> ____________ _________ _________ __
> From: usalymegirl <summersa@hotmail. com>
> To: LymeOz@yahoogroups. com.au
> Sent: Mon, 7 December, 2009 12:59:51 PM
> Subject: [LymeOz] Rosemary- Re: why is life so hard?
>
> �
> Hi Karin,
>
> I am new to LymeOz so we haven't spoken before. Your post really resonated with me, because I am struggling with staying positive as well. It is hard to see how far I have come in the past year.
>
> When you are living daily with pain, fatigue, brain fog it is only natural to lose perspective. That's why I like to check in with others to see what they have observed.
>
> I have been on abx for 12 months now and I have made progress. I am coming to the end of my first tx regimen and I am thinking about taking a break from the abx and trying the Salt/C protocol. I also have a rife machine and have been using that for 1 month.
>
> I want to wait until I am off abx to start the salt/c, that way I will know if the salt/c is working and won't get my progress confused with the abx.
>
> Hang in there and never, never give up!
> Aimee
>
> --- In LymeOz@yahoogroups. com.au, Karin Floate <karinfloate@ ...> wrote:
> >
> > �‚� Hi�‚� Aimee
> > �‚� We have not spocken before. Are you doing the s/c protocol, and how long. Thank's for the kind words.
> >
> > Karin
> >
> >
> >
> >
> > ____________ _________ _________ __
> > From: usalymegirl <summersa@ .>
> > To: LymeOz@yahoogroups. com.au
> > Sent: Thu, 3 December, 2009 7:51:28 PM
> > Subject: [LymeOz] Rosemary- Re: why is life so hard?
> >
> > �‚�
> > Karin,
> >
> > From personal experience I think it is hard to see our own progress b/c we live with this disease everyday. It is hard to be objective.
> >
> > The fact that your family has noticed changes and that you are driving again is HUGE - congrats.
> >
> > Maybe once a month you can check in with friends and family and ask their opinions on how you are doing. And ask how you are doing in relation to the previous month. That way when/if you have a bad day and get fustrated, you can remember that family and friends have noticed improvements.
> >
> > Aimee
> >
> > --- In LymeOz@yahoogroups. com.au, "Vic & Rosemary" <rosy1@> wrote:
> > >
> > > Hi Karin,
> > >
> > > I am so thrilled you can drive again. This is a huge step forward. Driving
> > > requires a lot of neurological functions.
> > >
> > > Best regards,
> > >
> > > Rosemary.
> > >
> > >
> > >
> > > _____
> > >
> > > From: LymeOz@yahoogroups. com.au [mailto:LymeOz@ yahoogroups. com.au] On Behalf
> > > Of Karin Floate
> > > Sent: Wednesday, 2 December 2009 10:51 AM
> > > To: LymeOz@yahoogroups. com.au
> > > Subject: Re: [LymeOz] Rosemary- Re: why is life so hard?
> > >
> > >
> > >
> > >
> > >
> > > Hi Leonnie
> > >
> > >
> > >
> > > How are you going with the s/c? Are you getting to the higher doses? My
> > > family and friends can see im provements, but I have trouble seeing it. But
> > > I can drive my car again, which I have not been able to do for 1 year. We
> > > really must have patience , and be percistent.
> > >
> > >
> > >
> > > Karin
> > >
> >
> >
> >
> >
> >
> > ____________ _________ _________ _________ _________ _________ _
> > Win 1 of 4 Sony home entertainment packs thanks to Yahoo!7.
> > Enter now: http://au.docs. yahoo.com/ homepageset/
> >
>
>
> ____________ _________ _________ __
> See what's on at the movies in your area. Find out now.
>
>
>
> ____________ _________ _________ _________ _________ _________ _
> See what's on at the movies in your area. Find out now: http://au.movies. yahoo.com/ session-times/
>

See what's on at the movies in your area. Find out now.

#1168

From: mualla akinci <muallaa@...>
Date: Wed Dec 23, 2009 3:01 am
Subject:: Re: Merry Christmas.

muallaa

Offline

Dear Lymeoz Members,

Wishing you a very merry Xmas and a very healthy 2010 and beyond

Best wishes

Marla

--- On Wed, 12/23/09, Vic & Rosemary <rosy1@...> wrote:

From: Vic & Rosemary <rosy1@...>
Subject: [LymeOz] Merry Christmas.
To: LymeOz@...
Date: Wednesday, December 23, 2009, 8:28 AM

Hi Gang,

Wishing you all a wonderful Christmas and a happy, healthy 2010,

Love,

Rosemary.

#1167

From: Karin Floate <karinfloate@...>
Date: Wed Dec 23, 2009 1:54 am
Subject:: Re: Cholestrymaine

karinfloate

Offline

Hi Nat.

x Karin

From: "natalieyoung@..." <natalieyoung@...>
To: LymeOz@...
Sent: Wed, 16 December, 2009 6:29:30 PM
Subject: Re: [LymeOz]Cholestrymaine

Hi Karin the cholestrymaine has helped with my pain thats for sure after 10 months of severe pain 8-10/10 everyday in just 7 weeks it has reduced to just 4/10 somedays less it hasnt however helped with muscle twitching and sore burning throat and abdomen spasms so my breathing is still crap and i am still fatigued however slightly less somewhat.

if you have etreme muscle and nerve pain give it a try its worth a bit of relief

nat young

--- In LymeOz@yahoogroups. com.au, Karin Floate <karinfloate@ ...> wrote:
>
> Â Hi everyone.
>
> Â I have been reading about Cholestyramine.Â Does it help with detox.?Â Does some one know more about it?
>
>
> thanks
> Karin
>
>
> ____________ _________ _________ __
> From: Karin Floate <karinfloate@ ...>
> To: LymeOz@yahoogroups. com.au
> Sent: Mon, 7 December, 2009 1:34:47 PM
> Subject: [LymeOz] hello aimee
>
> Â
> Â HiÂ Aimee
>
> Â Thank you for your e-mail. I am having a bad day to day, so glad that you have answered, some times the most comfort is from fellow sufferers. Have you been ill long, and can I ask where you live. I live inSydney, and removed a tick from Â my headÂ in September 2008, while spending a few days in QLD.Â Are you on more than 1 ABX?? How does one get through the day.??
>
> Â Kind regards
> Â Karin
>
>
>
>
> ____________ _________ _________ __
> From: usalymegirl <summersa@hotmail. com>
> To: LymeOz@yahoogroups. com.au
> Sent: Mon, 7 December, 2009 12:59:51 PM
> Subject: [LymeOz] Rosemary- Re: why is life so hard?
>
> Â
> Hi Karin,
>
> I am new to LymeOz so we haven't spoken before. Your post really resonated with me, because I am struggling with staying positive as well. It is hard to see how far I have come in the past year.
>
> When you are living daily with pain, fatigue, brain fog it is only natural to lose perspective. That's why I like to check in with others to see what they have observed.
>
> I have been on abx for 12 months now and I have made progress. I am coming to the end of my first tx regimen and I am thinking about taking a break from the abx and trying the Salt/C protocol. I also have a rife machine and have been using that for 1 month.
>
> I want to wait until I am off abx to start the salt/c, that way I will know if the salt/c is working and won't get my progress confused with the abx.
>
> Hang in there and never, never give up!
> Aimee
>
> --- In LymeOz@yahoogroups. com.au, Karin Floate <karinfloate@ ...> wrote:
> >
> > Ã‚Â HiÃ‚Â Aimee
> > Ã‚Â We have not spocken before. Are you doing the s/c protocol, and how long. Thank's for the kind words.
> >
> > Karin
> >
> >
> >
> >
> > ____________ _________ _________ __
> > From: usalymegirl <summersa@ .>
> > To: LymeOz@yahoogroups. com.au
> > Sent: Thu, 3 December, 2009 7:51:28 PM
> > Subject: [LymeOz] Rosemary- Re: why is life so hard?
> >
> > Ã‚Â
> > Karin,
> >
> > From personal experience I think it is hard to see our own progress b/c we live with this disease everyday. It is hard to be objective.
> >
> > The fact that your family has noticed changes and that you are driving again is HUGE - congrats.
> >
> > Maybe once a month you can check in with friends and family and ask their opinions on how you are doing. And ask how you are doing in relation to the previous month. That way when/if you have a bad day and get fustrated, you can remember that family and friends have noticed improvements.
> >
> > Aimee
> >
> > --- In LymeOz@yahoogroups. com.au, "Vic & Rosemary" <rosy1@> wrote:
> > >
> > > Hi Karin,
> > >
> > > I am so thrilled you can drive again. This is a huge step forward. Driving
> > > requires a lot of neurological functions.
> > >
> > > Best regards,
> > >
> > > Rosemary.
> > >
> > >
> > >
> > > _____
> > >
> > > From: LymeOz@yahoogroups. com.au [mailto:LymeOz@ yahoogroups. com.au] On Behalf
> > > Of Karin Floate
> > > Sent: Wednesday, 2 December 2009 10:51 AM
> > > To: LymeOz@yahoogroups. com.au
> > > Subject: Re: [LymeOz] Rosemary- Re: why is life so hard?
> > >
> > >
> > >
> > >
> > >
> > > Hi Leonnie
> > >
> > >
> > >
> > > How are you going with the s/c? Are you getting to the higher doses? My
> > > family and friends can see im provements, but I have trouble seeing it. But
> > > I can drive my car again, which I have not been able to do for 1 year. We
> > > really must have patience , and be percistent.
> > >
> > >
> > >
> > > Karin
> > >
> >
> >
> >
> >
> >
> > ____________ _________ _________ _________ _________ _________ _
> > Win 1 of 4 Sony home entertainment packs thanks to Yahoo!7.
> > Enter now: http://au.docs. yahoo.com/ homepageset/
> >
>
>
> ____________ _________ _________ __
> See what's on at the movies in your area. Find out now.
>
>
>
> ____________ _________ _________ _________ _________ _________ _
> See what's on at the movies in your area. Find out now: http://au.movies. yahoo.com/ session-times/
>

See what's on at the movies in your area. Find out now.

#1166

From: Karin Floate <karinfloate@...>
Date: Wed Dec 23, 2009 1:42 am
Subject:: Re: Merry Christmas.

karinfloate

Offline

Hi all

Wishing every one a wonderful Chrismas , special thanks to my supporters and hope fully a health new year for all of us.

Love Karin

From: Vic & Rosemary <rosy1@...>
To: LymeOz@...
Sent: Wed, 23 December, 2009 8:28:25 AM
Subject: [LymeOz] Merry Christmas.

Hi Gang,

Wishing you all a wonderful Christmas and a happy, healthy 2010,

Love,

Rosemary.

See what's on at the movies in your area. Find out now.

#1165

From: "Vic & Rosemary" <rosy1@...>
Date: Tue Dec 22, 2009 9:28 pm
Subject:: Merry Christmas.

aussietickchick

Offline

Hi Gang,

Wishing you all a wonderful Christmas and a happy, healthy 2010,

Love,

Rosemary.

#1164

From: "Vic & Rosemary" <rosy1@...>
Date: Thu Dec 17, 2009 4:25 am
Subject:: RE: vic and rosemary

aussietickchick

Offline

Hi Nat,

I was misdiagnosed for 22 years so I did not get proper treatment until the last few years.

I take 1 gram of each salt & vitamin C per dose. I take about 10 doses per day or more if I can.

Yes, I knew it was working from the very 1^st day.

Yes, you just need to use the correct frequencies which are listed in instruction manuals and on the internet.

Rosemary.

From: LymeOz@... [mailto:LymeOz@...] On Behalf Of natalieyoung@...
Sent: Thursday, 17 December 2009 10:05 AM
To: LymeOz@...
Subject: [LymeOz] vic and rosemary

thanks vic and rosemary 25 years of the throat thing oh no!

what strength salt c do you take i am going to have a break from antibiotics next year some time and try it out

do you notice any changes in a reasonably small amount of time? or does it take 25 years?

Do you know if rife can also target co infections?

nat

#1163

From: "rhondamurphy5655" <rhondamurphy5655@...>
Date: Thu Dec 17, 2009 1:15 am
Subject:: Re: Re rife machine where and which ones to buy?

rhondamurphy...

Offline

Hi Nat,

i have started Rife treatment - had my 3rd session yesterday. My homeopath is
using a F- Scan compact which he got through a naturopath in Adelaide who has a
clinic which focus' on rife treatment. i think it came in from Germany.

It is mentioned in Bryan rosners book but it is discussed as apromising machine.
I think it was relatively new when the book was written. It is very compact. I
have been having 1 treatment a week ranging from approx 1hr until yesterday
which was 1and1/2
hrs. Phillip has been advised to treat me for approx an hour twice a weweek for
good results. He is hiring the machine out to me next week and i think he wants
me to use it evry 2nd day with different frquencies. He will go throught it on
wed. the machine scans your body first the treats anything showing up and then
you go on to treating lyme etc. I'll let you know more once I have to do it for
myself. fortunately Gavan wil be going with me on wed so he should remember what
to do.

I had about 12 hrs feeling great last thurs but then went backwards adn was
really bad sat improved but weak and tired sunday and expected to be better
again on Monday but was worse thids seems to be a reasonably strong reaction at
the moment. apparently this is good.

rhonda
--- In LymeOz@..., "natalieyoung@..." <natalieyoung@...> wrote:
>
> Hi people anyone know much about rife and which is a brand or name that has
proven capabilities?
>
> nat
>

#1162

From: "rhondamurphy5655" <rhondamurphy5655@...>
Date: Thu Dec 17, 2009 1:04 am
Subject:: Re: sore throats burning mouth throat

rhondamurphy...

Offline

hi nat,

yes I often have the constant burning throat and mouth and it goes down into my
chest.Just when i think it has gone it reappears. Breathing difficulties aren't
as bad or as constant.

rhonda

--- In LymeOz@..., "natalieyoung@..." <natalieyoung@...> wrote:
>
> Does anyone suffer from constant sore throat burning throat and mouth, and
breathing irregularities?
>
> it sort of feels as though i have something in  base of my my throat where my
glands are stopping me from breathing properly hard to explain
>
> nat
>

#1161

From: "natalieyoung@..." <natalieyoung@...>
Date: Wed Dec 16, 2009 11:05 pm
Subject:: vic and rosemary

natalieyoung...

Offline

thanks vic and rosemary 25 years of the throat thing oh no!

what strength salt c do you take i am going to have a break from antibiotics
next year some time and try it out

do you notice any changes in a reasonably small amount of time? or does it take
25 years?

Do you know if rife can also target co infections?

nat

#1160

From: "Vic & Rosemary" <rosy1@...>
Date: Wed Dec 16, 2009 10:04 am
Subject:: RE: Re rife machine where and which ones to buy?

aussietickchick

Offline

Hi Nat,

Yes, I studied Rife for years and was with a Rife-Lyme support group. Rife uses low frequency radio waves to kill bacteria. The 3 top machines known for killing Lyme are the “Doug” coil, the Ultimate B3 (which I have) and the EmEm. Many others were tried, but these 3 machines are known for killing Lyme. I bought my UB3 from Utah. The company has since updated this model to a GB4000. I was having little seizures for over 10 years and abx had not helped. With my very 1^st Rife session the seizures stopped and have not returned. I totally believe in Rife. My UB3 is a pad device where you hold onto metal cylinders and put your feet on metal plates to create a circuit. You can buy a plasma machine where you don’t have to touch anything and the radio waves go right through you. These are also good. It is hard to get a Rife machine in Oz.

I had a lot of trouble with my Aussie (made in China) adapters and my machine kept breaking down. I was relapsing, and was too sick to realize why. It was during this time that I discovered salt & C which has worked wonders for me.

Meanwhile someone in the company sent me an adapter which was not suitable and basically blew up my Rife machine. The boss realized the problem and sent me out a brand new machine with a really excellent adapter, so it works perfectly and better than ever. Because the salt & C was working for me, I have not used Rife much, so the machine is almost brand new. I am considering selling it.

If anyone is in Melbourne and would like to try it out, feel free to contact me. If you can get to Mount Eliza, you can try it free of charge.

I believe we need to hit Lyme and co with everything we can cope with. Some people even do Rife with salt & C.

Rosemary.

From: LymeOz@... [mailto:LymeOz@...] On Behalf Of natalieyoung@...
Sent: Wednesday, 16 December 2009 6:41 PM
To: LymeOz@...
Subject: [LymeOz] Re rife machine where and which ones to buy?

Hi people anyone know much about rife and which is a brand or name that has proven capabilities?

nat

#1159

From: "Vic & Rosemary" <rosy1@...>
Date: Wed Dec 16, 2009 9:48 am
Subject:: RE: sore throats burning mouth throat

aussietickchick

Offline

Hi Nat,

Yes, I had these symptoms for over 25 years. It was absolutely horrible. Salt & C has brought me a long way. I am not 100%, but many days I almost feel normal. Just keep killing the bugs.

Rosemary.

From: LymeOz@... [mailto:LymeOz@...] On Behalf Of natalieyoung@...
Sent: Wednesday, 16 December 2009 6:32 PM
To: LymeOz@...
Subject: [LymeOz] sore throats burning mouth throat

Does anyone suffer from constant sore throat burning throat and mouth, and breathing irregularities?

it sort of feels as though i have something in base of my my throat where my glands are stopping me from breathing properly hard to explain

nat

#1158

From: "natalieyoung@..." <natalieyoung@...>
Date: Wed Dec 16, 2009 7:41 am
Subject:: Re rife machine where and which ones to buy?

natalieyoung...

Offline

Hi people anyone know much about rife and which is a brand or name that has
proven capabilities?

nat

#1157

From: "natalieyoung@..." <natalieyoung@...>
Date: Wed Dec 16, 2009 7:32 am
Subject:: sore throats burning mouth throat

natalieyoung...

Offline

Does anyone suffer from constant sore throat burning throat and mouth, and
breathing irregularities?

it sort of feels as though i have something in  base of my my throat where my
glands are stopping me from breathing properly hard to explain

nat

#1156

From: "natalieyoung@..." <natalieyoung@...>
Date: Wed Dec 16, 2009 7:29 am
Subject:: Re: Cholestrymaine

natalieyoung...

Offline

Hi Karin the cholestrymaine has helped with my pain thats for sure after 10
months of severe pain 8-10/10 everyday in just 7 weeks it has reduced to just
4/10 somedays less it hasnt however helped with muscle twitching and sore
burning throat and abdomen spasms so my breathing is still crap  and i am still
fatigued however slightly less somewhat.

if you have etreme muscle and nerve pain give it a try its worth a bit of relief

nat young

--- In LymeOz@..., Karin Floate <karinfloate@...> wrote:
>
>  Hi everyone.
>
>  I have been reading about Cholestyramine.  Does it help with detox.? Does
some one know more about it?
>
>
> thanks
> Karin
>
>
> ________________________________
> From: Karin Floate <karinfloate@...>
> To: LymeOz@...
> Sent: Mon, 7 December, 2009 1:34:47 PM
> Subject: [LymeOz] hello aimee
>
>  
>  Hi  Aimee
>
>  Thank you for your e-mail. I am having a bad day to day, so glad that you
have answered, some times the most comfort is from fellow sufferers. Have you
been ill long, and can I ask where you live. I live inSydney, and removed a tick
from  my head  in September 2008, while spending a few days in QLD.  Are you
on more than 1 ABX?? How does one get through the day.??
>
>  Kind regards
>  Karin
>
>
>
>
> ________________________________
> From: usalymegirl <summersa@hotmail. com>
> To: LymeOz@yahoogroups. com.au
> Sent: Mon, 7 December, 2009 12:59:51 PM
> Subject: [LymeOz] Rosemary- Re: why is life so hard?
>
>  
> Hi Karin,
>
> I am new to LymeOz so we haven't spoken before. Your post really resonated
with me, because I am struggling with staying positive as well. It is hard to
see how far I have come in the past year.
>
> When you are living daily with pain, fatigue, brain fog it is only natural to
lose perspective. That's why I like to check in with others to see what they
have observed.
>
> I have been on abx for 12 months now and I have made progress. I am coming to
the end of my first tx regimen and I am thinking about taking a break from the
abx and trying the Salt/C protocol. I also have a rife machine and have been
using that for 1 month.
>
> I want to wait until I am off abx to start the salt/c, that way I will know if
the salt/c is working and won't get my progress confused with the abx.
>
> Hang in there and never, never give up!
> Aimee
>
> --- In LymeOz@yahoogroups. com.au, Karin Floate <karinfloate@ ...> wrote:
> >
> > Â HiÂ  Aimee
> > Â We have not spocken before. Are you doing the s/c protocol, and how
long. Thank's for the kind words.
> >
> > Karin
> >
> >
> >
> >
> > ____________ _________ _________ __
> > From: usalymegirl <summersa@ .>
> > To: LymeOz@yahoogroups. com.au
> > Sent: Thu, 3 December, 2009 7:51:28 PM
> > Subject: [LymeOz] Rosemary- Re: why is life so hard?
> >
> > Â 
> > Karin,
> >
> > From personal experience I think it is hard to see our own progress b/c we
live with this disease everyday. It is hard to be objective.
> >
> > The fact that your family has noticed changes and that you are driving again
is HUGE - congrats.
> >
> > Maybe once a month you can check in with friends and family and ask their
opinions on how you are doing. And ask how you are doing in relation to the
previous month. That way when/if you have a bad day and get fustrated, you can
remember that family and friends have noticed improvements.
> >
> > Aimee
> >
> > --- In LymeOz@yahoogroups. com.au, "Vic & Rosemary" <rosy1@> wrote:
> > >
> > > Hi Karin,
> > >
> > > I am so thrilled you can drive again. This is a huge step forward. Driving
> > > requires a lot of neurological functions.
> > >
> > > Best regards,
> > >
> > > Rosemary.
> > >
> > >
> > >
> > > _____
> > >
> > > From: LymeOz@yahoogroups. com.au [mailto:LymeOz@ yahoogroups. com.au] On
Behalf
> > > Of Karin Floate
> > > Sent: Wednesday, 2 December 2009 10:51 AM
> > > To: LymeOz@yahoogroups. com.au
> > > Subject: Re: [LymeOz] Rosemary- Re: why is life so hard?
> > >
> > >
> > >
> > >
> > >
> > > Hi Leonnie
> > >
> > >
> > >
> > > How are you going with the s/c? Are you getting to the higher doses? My
> > > family and friends can see im provements, but I have trouble seeing it.
But
> > > I can drive my car again, which I have not been able to do for 1 year. We
> > > really must have patience , and be percistent.
> > >
> > >
> > >
> > > Karin
> > >
> >
> >
> >
> >
> >
> > ____________ _________ _________ _________ _________ _________ _
> > Win 1 of 4 Sony home entertainment packs thanks to Yahoo!7.
> > Enter now: http://au.docs. yahoo.com/ homepageset/
> >
>
>
> ________________________________
> See what's on at the movies in your area. Find out now.
>
>
>
>      
________________________________________________________________________________\
__
> See what's on at the movies in your area. Find out now:
http://au.movies.yahoo.com/session-times/
>

#1155

From: Karin Floate <karinfloate@...>
Date: Mon Dec 14, 2009 10:46 pm
Subject:: Re: Questran.

karinfloate

Offline

Thank you Rosemary.

Karin

From: Vic & Rosemary <rosy1@...>
To: LymeOz@...
Sent: Mon, 14 December, 2009 9:56:33 PM
Subject: [LymeOz] Questran.

Hi Karin,

I tried Questran (cholestyramine) for 6 months. It didn’t do much for me, but it really does help some people. It absorbs toxins and carries them out through the stool. You can find more info at http://www.chronicn eurotoxins. com/info/ research. cfm

It is certainly worth trying. Just make sure you drink plenty of water and don’t get constipated.

Rosemary.

From: LymeOz@yahoogroups. com.au [mailto: LymeOz@yahoogroups. com.au ] On Behalf Of Karin Floate
Sent: Monday, 14 December 2009 6:58 PM
To: LymeOz@yahoogroups. com.au
Subject: Re: [LymeOz]

Hi everyone.

I have been reading about Cholestyramine. Does it help with detox.? Does some one know more about it?

thanks

Karin

See what's on at the movies in your area. Find out now.

#1154

From: "Vic & Rosemary" <rosy1@...>
Date: Mon Dec 14, 2009 10:56 am
Subject:: Questran.

aussietickchick

Offline

Hi Karin,

It is certainly worth trying. Just make sure you drink plenty of water and don’t get constipated.

Rosemary.

From: LymeOz@... [mailto:LymeOz@...] On Behalf Of Karin Floate
Sent: Monday, 14 December 2009 6:58 PM
To: LymeOz@...
Subject: Re: [LymeOz]

Hi everyone.

I have been reading about Cholestyramine. Does it help with detox.? Does some one know more about it?

thanks

Karin

#1153

From: Karin Floate <karinfloate@...>
Date: Mon Dec 14, 2009 7:58 am
Subject:: Re:

karinfloate

Offline

Hi everyone.

I have been reading about Cholestyramine. Does it help with detox.? Does some one know more about it?

thanks

Karin

From: Karin Floate <karinfloate@...>
To: LymeOz@...
Sent: Mon, 7 December, 2009 1:34:47 PM
Subject: [LymeOz] hello aimee

Hi Aimee

Thank you for your e-mail. I am having a bad day to day, so glad that you have answered, some times the most comfort is from fellow sufferers. Have you been ill long, and can I ask where you live. I live inSydney, and removed a tick from my head in September 2008, while spending a few days in QLD. Are you on more than 1 ABX?? How does one get through the day.??

Kind regards

Karin

From: usalymegirl <summersa@hotmail. com>
To: LymeOz@yahoogroups. com.au
Sent: Mon, 7 December, 2009 12:59:51 PM
Subject: [LymeOz] Rosemary- Re: why is life so hard?

Hi Karin,

I am new to LymeOz so we haven't spoken before. Your post really resonated with me, because I am struggling with staying positive as well. It is hard to see how far I have come in the past year.

When you are living daily with pain, fatigue, brain fog it is only natural to lose perspective. That's why I like to check in with others to see what they have observed.

I have been on abx for 12 months now and I have made progress. I am coming to the end of my first tx regimen and I am thinking about taking a break from the abx and trying the Salt/C protocol. I also have a rife machine and have been using that for 1 month.

I want to wait until I am off abx to start the salt/c, that way I will know if the salt/c is working and won't get my progress confused with the abx.

Hang in there and never, never give up!
Aimee

--- In LymeOz@yahoogroups. com.au, Karin Floate <karinfloate@ ...> wrote:
>
> Â HiÂ Aimee
> Â We have not spocken before. Are you doing the s/c protocol, and how long. Thank's for the kind words.
>
> Karin
>
>
>
>
> ____________ _________ _________ __
> From: usalymegirl <summersa@.. .>
> To: LymeOz@yahoogroups. com.au
> Sent: Thu, 3 December, 2009 7:51:28 PM
> Subject: [LymeOz] Rosemary- Re: why is life so hard?
>
> Â
> Karin,
>
> From personal experience I think it is hard to see our own progress b/c we live with this disease everyday. It is hard to be objective.
>
> The fact that your family has noticed changes and that you are driving again is HUGE - congrats.
>
> Maybe once a month you can check in with friends and family and ask their opinions on how you are doing. And ask how you are doing in relation to the previous month. That way when/if you have a bad day and get fustrated, you can remember that family and friends have noticed improvements.
>
> Aimee
>
> --- In LymeOz@yahoogroups. com.au, "Vic & Rosemary" <rosy1@> wrote:
> >
> > Hi Karin,
> >
> > I am so thrilled you can drive again. This is a huge step forward. Driving
> > requires a lot of neurological functions.
> >
> > Best regards,
> >
> > Rosemary.
> >
> >
> >
> > _____
> >
> > From: LymeOz@yahoogroups. com.au [mailto:LymeOz@ yahoogroups. com.au] On Behalf
> > Of Karin Floate
> > Sent: Wednesday, 2 December 2009 10:51 AM
> > To: LymeOz@yahoogroups. com.au
> > Subject: Re: [LymeOz] Rosemary- Re: why is life so hard?
> >
> >
> >
> >
> >
> > Hi Leonnie
> >
> >
> >
> > How are you going with the s/c? Are you getting to the higher doses? My
> > family and friends can see im provements, but I have trouble seeing it. But
> > I can drive my car again, which I have not been able to do for 1 year. We
> > really must have patience , and be percistent.
> >
> >
> >
> > Karin
> >
>
>
>
>
>
> ____________ _________ _________ _________ _________ _________ _
> Win 1 of 4 Sony home entertainment packs thanks to Yahoo!7.
> Enter now: http://au.docs. yahoo.com/ homepageset/
>

See what's on at the movies in your area. Find out now.

#1152

From: "Vic & Rosemary" <rosy1@...>
Date: Tue Dec 8, 2009 7:39 am
Subject:: Babesia e-book FREE download.

aussietickchick

Offline

http://ebooks.hopeacademic.com/BabesiaUpdate2009-Ebook.pdf

FREE 2009 UPDATED BABESIA TEXTBOOK

Dr. Schaller has decided to give access to his latest book, the 2009 Babesia Update free to anyone who needs or wants to read it. Even given the immense sacrifice of time and cost to him personally, his continued and growing awareness of the many people sick with Babesia has prompted him to give out the information to save as many lives as possible. For those of you who read the first book, The Diagnosis and Treatment of Babesia – which has much useful information that should not be ignored and is not included in this book – you will understand why he is so passionate. His son, Jeremy, would not have survived had he not taken up the mallet and strove to find successful ways of treating this illness. Jeremy is alive, healthy and a wonderful young man thanks to his Father’s care and hard work.

IF YOU FORWARD OR POST THE BOOK, THIS LETTER MUST BE POSTED WITH THE FREE BOOK.

For those of you unfamiliar with the publishing world, please know that unless your name is Dr. Phil, Hillary, Suzanne or Oprah, books on super specific issues do not sell and do not make money or even remotely come close to breaking even.

Any money being made from selling this book is certainly not worth one life. It is not worth one person becoming disabled and non-functional for years or decades.

http://ebooks.hopeacademic.com/BabesiaUpdate2009-Ebook.pdf

BASED ON YEARS OF RESEARCH, STUDY OF VIRTUALLY ALL MAJOR PUBLISHED SCIENTIFIC/MEDICAL LITERATURE

TREATMENTS BASED ON INHERITED TREATMENT FAILURES

NEW LAB TESTING OPTIONS WHICH MIGHT CATCH THE CAUSE OF LOST PROGRESS OR RELAPSE

****

THE COPYRIGHT STAYS IN PLACE, BUT IS NOT VIOLATED IF YOU ONLY USE THE TEXTBOOK FOR YOUR OWN PERSONAL USE.

FEEL FREE TO PRINT THE BOOK.

WHILE YOU HAVE NO PERMISSION TO SELL THIS BOOK, YOU CAN GIVE IT TO ANYONE FOR FREE. IT CAN BE FORWARDED WITHOUT LIMIT TO AS MANY PEOPLE AS YOU THINK SHOULD READ IT OR WHO HAVE SYMPTOMS THEY ARE IGNORING. (TICK INFECTIONS DECREASE INSIGHT).

PLEASE DO NOT ALTER THE TEXT.

Babesia can cause death, disability, obesity, serious fatigue, migraine torture and a hundred other medical problems. The information needs to be free to everyone.

We also hope it will help some interested healers catch stealth Babesia more often, because we feel it is common, and not an occasional finding in a Lyme positive patient. Many new Babesia species are being found in humans even in the last four years, so the list of human Babesia species and their variants is not finalized

Finally, the cost for top laboratories to keep up and have perfect diagnostic testing is an unrealistic expectation, so other new ideas are included to help show low levels of Babesia that have significant body effects, based on solid research articles.

PLEASE DO NOT SELF TREAT BASED ON THIS BOOK.

NO INFORMATION IS MEANT TO BE AUTHORITATIVE AND ALL CARE IS UNDER THE SUPERVISION OF A LICENSED MEDICAL WORKER.

Be Better!! Be Well!

Rona. C., MBA

Office Manager

Survivor of Lyme, Bartonella, Babesia Microti and Babesia Duncani!

IF YOU FORWARD OR POST THE BOOK, THIS LETTER MUST BE POSTED WITH THE FREE BOOK.

Reply | Forward | Messages in this Topic (1)

#1151

From: "Vic & Rosemary" <rosy1@...>
Date: Tue Dec 8, 2009 7:24 am
Subject:: Under Our Skin.

aussietickchick

Offline

http://neuro-lyme.com/videoblog/under-our-skin-filmmaker-discusses-lyme-disease

Hi Gang,

Filmmaker, Andy Abrahams Wilson talks about his recently completed documentary, “Under Our Skin,” which explores Lyme Disease.

Rosemary.

#1150

From: "rhondamurphy5655" <rhondamurphy5655@...>
Date: Tue Dec 8, 2009 1:05 am
Subject:: Rhonda/Re:glutathione and detoxing

rhondamurphy...

Offline

hi Leonie,

it would be great if you could send me more info. i'm seing my homeopath
tomorrow for my 2nd Rife treatment so i'll discuss it with him as well as i need
to rder something to have before christmas. i sent him an email last night
telling him about the situation with glutathione in vic so he can be ready to
discuss with me tomorrw. Onwe thing i've discovered is nothing is cheap when
treating lyme and co. although I now order a lot of my supplements from i-herd
and they are cheaper that way. my integrative gp was very expensive - the co-Q10
was about $90 from him and in the health food shop about 50 before i got my
discount for the same brand. I'm now using another brand from the US which is
cheaper and i hope just as effective.

look forward to hearing from you

rhonda

--- In LymeOz@..., "leonie cent" <leoniecent@...> wrote:
>
> Hi Rhonda,
>
> I have been trialing a few glutathione products recently. One was Immunocal
and the other Max GXL.  Both are MLM type companies so therefore quite
expensive.  They are both designed as precursors to glutathione, because as you
say, the body doesnt absorb glutathione in a supplement.  I've tried both
products and feel they are both very good.  They each disparage the other
company which is typical of MLM businesses. They are both hard to get because
they come out of the USA and Canada, but there's a lady i found online who sells
the Immunocal from Victoria - another guy sells it out of Sydney but he is more
expensive - if you want their details let me know.  It's a protein powder that
you make into a drink.  It uses special technology or something? so that it
delivers cysteine to the body, therefore creating glutathione.  I didnt try it
long enough to really know an awful lot about how good it is, but did feel that
it was doing something positive.  The other product, Max, is just about to be
launched in Australia - I'm trying that one right now and it did actually help
me in a way i noticed quite quickly.  At the moment it gets shipped in from
Canada or the USA.  It's all over the net and you could order it that way.  I'm
about to sign up with the company so that i can buy it at the cheap price and
save money.  If you're interested, let me know and i'll see that you get it at
the cheap price too. I have lots of info on both products if you want to read
anything - let me know if you want me to send more info.
>
> best,
> Leonie
> leoniecent@...
>

#1149

From: "leonie cent" <leoniecent@...>
Date: Mon Dec 7, 2009 10:27 am
Subject:: Rhonda/Re:glutathione and detoxing

mumpup2000

Offline

Hi Rhonda,

I have been trialing a few glutathione products recently. One was Immunocal and the other Max GXL. Both are MLM type companies so therefore quite expensive. They are both designed as precursors to glutathione, because as you say, the body doesnt absorb glutathione in a supplement. I've tried both products and feel they are both very good. They each disparage the other company which is typical of MLM businesses. They are both hard to get because they come out of the USA and Canada, but there's a lady i found online who sells the Immunocal from Victoria - another guy sells it out of Sydney but he is more expensive - if you want their details let me know. It's a protein powder that you make into a drink. It uses special technology or something? so that it delivers cysteine to the body, therefore creating glutathione. I didnt try it long enough to really know an awful lot about how good it is, but did feel that it was doing something positive. The other product, Max, is just about to be launched in Australia - I'm trying that one right now and it did actually help me in a way i noticed quite quickly. At the moment it gets shipped in from Canada or the USA. It's all over the net and you could order it that way. I'm about to sign up with the company so that i can buy it at the cheap price and save money. If you're interested, let me know and i'll see that you get it at the cheap price too. I have lots of info on both products if you want to read anything - let me know if you want me to send more info.

best,

Leonie

leoniecent@...

#1148

From: "rhondamurphy5655" <rhondamurphy5655@...>
Date: Mon Dec 7, 2009 5:29 am
Subject:: glutathione and detoxing

rhondamurphy...

Offline

Hi Everyone,

does anyone know anything about glutathione for detoxing with herx reactions. i
have been told i need to take this supplement while on rife therapy to get rid
of the toxins. It is not available in Victoria so i will have to get it from
interstate or the USA. when I checked Kenneth singleton's book it said that the
oral form is not very well absorbed in the gut. apparently you can get it in
sub-lingual or transdermal forms(patches). I would be grateful for any info on
these regarding brands and recommended places to get it( especially with
Christmas being so close and having already started treatment).

thanks

Rhonda

Reply | Forward | Messages in this Topic (1)

#1147

From: Karin Floate <karinfloate@...>
Date: Mon Dec 7, 2009 2:34 am
Subject:: hello aimee

karinfloate

Offline

Hi Aimee

Kind regards

Karin

From: usalymegirl <summersa@...>
To: LymeOz@...
Sent: Mon, 7 December, 2009 12:59:51 PM
Subject: [LymeOz] Rosemary- Re: why is life so hard?

See what's on at the movies in your area. Find out now.