Re: Re: Someone wants to join Rogene

[Guest guest]

What does " herxing " mean?

--- mikat828 <mikat828@...> wrote:

>

> Hi Sue

> I just wanted you to know that I am always thinking

> of you and

> praying for you. Hopefully it won't be much longer

> before you will

> be making progress again towards getting better.

> Sometimes we take

> downhill turns and can't figure out why, but

> eventually things turn

> around.I have a friend doing a treatment that

> consists of salt and

> vitamin C and she has been doing this for 21 months.

> In that

> time,she has been herxing almost constantly, often

> with severe

> headaches. I was reading her posts with interest

> because she had

> been on the antibiotic protocol site before that but

> had back

> slidden and felt that she was getting worse again to

> the point of no

> hope. She was in a wheel chair at this point. She

> had had lyme for

> 17 years (misdiagnosed) and never remembered being

> bitten by a

> tick. She swears she got as sexually transmitted

> from her husband

> who was eventually diagnosed with lyme. Anyway, the

> salt/C has

> provided her tremendous improvement and her

> headaches are gone. She

> is not well yet, but her life is so much better.

> The two things to

> take away from this person's experience is that

> first, we can herx

> for a very long time and not know it. Many many

> people on this site

> herx pretty much continuously for wellover a year.

> Second, if one

> thing appears to have stopped working, or isn't

> working, there is

> always a way to tweak it or try something else that

> will get you

> back on the path to healing! I know a woman with

> fast progressing

> scleroderma who wasn't helped with one protocol and

> switched to the

> Marshall Protocol and is doing very well now. We

> just have to keep

> searching and trying things and never give up!!

> Stay encouraged. I

> am so glad that Rogene will be visiting you . That

> is awesome! I

> wish I could go back to England. I loved it back in

> 2000 when we

> toured europe. Take care and God bless.

> Kathy

>

>

>

>

>

>

>

>

> >

> > Hi Rogene,

> >

> > Its funny you should talk about orange juice, I

> only ever drink

> water but as

> > I have very little calcium intake as I react to

> milk I have

> started drinking

> > something called Tropicana which is orange with

> added calcium,

> gave me

> > that tip from her ME specialist.

> > I will ask my Dr if she would be willing to speak

> with Dr Kolb via

> email but

> > I have my doubts as Myhill wrote to her a

> few years back and

> she

> > pretty much pooh whooed it, and said I didn't have

> ME, she asked

> why I was wasting

> > my money paying for a private Dr when there was no

> evidence to

> prove the

> > silicone link, but I will try again.

> > I will see if I can get the grapefruit extract, I

> have not seen it

> but will

> > try to locate it.

> >

> > I am really looking forward to finding out what

> Shari finds out.

> > I will email you tomorrow with my blood results,

> finger crossed.

> >

> > Sue.

> >

>

>

>

>

>

__________________________________________________

[Guest guest]

I looked it up....sorry, I realize now it is the low dose antibiotics that you've talked about before, and which I know you've been on. Are you still taking them at all? PattyTricia Trish <glory2glory1401@...> wrote: Kathy, What exactly is the Marshall protocol? Pattymikat828 <mikat828 > wrote: Hi SueI just wanted you to know that I am always thinking of you and praying for you. Hopefully it won't be much longer before you will be making progress again towards getting better. Sometimes we take downhill turns and can't figure out why, but eventually things turn around.I have a friend doing a treatment that consists of salt and vitamin C and she has been doing this for 21 months. In that time,she has been herxing almost constantly, often with severe headaches. I was reading her posts with interest because she had been on the antibiotic protocol site before that but had back slidden and felt that she was getting worse again to the point of no hope. She was in a wheel chair at this point. She had had lyme for 17 years (misdiagnosed) and never remembered being bitten by a tick. She swears she got as sexually transmitted from her husband who was eventually diagnosed with lyme. Anyway, the salt/C has

provided her tremendous improvement and her headaches are gone. She is not well yet, but her life is so much better. The two things to take away from this person's experience is that first, we can herx for a very long time and not know it. Many many people on this site herx pretty much continuously for wellover a year. Second, if one thing appears to have stopped working, or isn't working, there is always a way to tweak it or try something else that will get you back on the path to healing! I know a woman with fast progressing scleroderma who wasn't helped with one protocol and switched to the Marshall Protocol and is doing very well now. We just have to keep searching and trying things and never give up!! Stay encouraged. I am so glad that Rogene will be visiting you . That is awesome! I wish I could go back to England. I loved it back in 2000 when we toured europe. Take care and God bless.Kathy>> Hi Rogene, > > Its funny you should talk about orange juice, I only ever drink water but as > I have very little calcium intake as I react to milk I have started drinking > something called Tropicana which is orange with added calcium, gave me > that tip from her ME specialist. > I will ask my Dr if she would be willing to speak with Dr Kolb via email but > I have my doubts as Myhill wrote to her a few years back and she > pretty much pooh whooed it, and said I didn't have ME, she asked why I was wasting > my money paying for a private Dr when there was no evidence to prove the > silicone link, but I will try again.> I will see if I can get the grapefruit extract, I have not seen it but will > try to locate it.>

> I am really looking forward to finding out what Shari finds out.> I will email you tomorrow with my blood results, finger crossed.> > Sue.> Do you ?Everyone is raving about the all-new Beta. __________________________________________________