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Dear Judy,

Hi, I'm so glad to hear your good news. I remember when you wrote about

your relapse and how concerned you were in your earlier history.

Congratulations on the good new, right off the press. PCRU is the holy grail

and the 2 years will pass quickly. It gives us all hope, Judy, that even with

all the adversity you have had to face, you can still come out on top, as you

have. You are beating back the dragon. One day we will all say in unison,

hail, hail, the dragon is dead. Hope you enjoyed your family celebration. In

our circle, people who are able to beat back the dragon become icons. We will

all be sporting " JUDY WON " pins. LOL.

Blessings and all best wishes,

Lottie

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  • 1 year later...
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any extra stress in your life

>

> I started LDN about 1 1/2 years ago. I have RRMS, transverse myelitis,

Fibromyalgia and C.F.I.D.S. The first year was great. I had no relapses and had

more endurance and stamina. Then it felt as though it started wearing off. I

have new lesions. Since January I've had three relapses. I'm having one now.

I've been on 3.5 mg.

> I follow an anti-candida diet and MS diet. I take supplements, vitamins, fish

oil, evening primrose oil, etc. Any ideas? Dosage suggestions? I'm thinking of

starting Copaxone. I was hoping to not have to do injections anymore.

>

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> >

> > I started LDN about 1 1/2 years ago. I have RRMS, transverse myelitis,

Fibromyalgia and C.F.I.D.S. The first year was great. I had no relapses and had

more endurance and stamina. Then it felt as though it started wearing off. I

have new lesions. Since January I've had three relapses. I'm having one now.

I've been on 3.5 mg.

> > I follow an anti-candida diet and MS diet. I take supplements, vitamins,

fish oil, evening primrose oil, etc. Any ideas? Dosage suggestions? I'm thinking

of starting Copaxone. I was hoping to not have to do injections anymore.

> >

>have you tried 4.5 mg? or has your supplier or pharmacy changed?

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> >

> > I started LDN about 1 1/2 years ago. I have RRMS, transverse myelitis,

Fibromyalgia and C.F.I.D.S. The first year was great. I had no relapses and had

more endurance and stamina. Then it felt as though it started wearing off. I

have new lesions. Since January I've had three relapses. I'm having one now.

I've been on 3.5 mg.

> > I follow an anti-candida diet and MS diet. I take supplements, vitamins,

fish oil, evening primrose oil, etc. Any ideas? Dosage suggestions? I'm thinking

of starting Copaxone. I was hoping to not have to do injections anymore.

> >

>have you tried 4.5 mg? or has your supplier or pharmacy changed?

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Make sure there have been no changes in your LDN script and that you are getting

LDN from a reputable compounding pharmacy. Why are you not taking 4.5mg LDN?

To be positive you do not have yeast problems see below on what tests should be

done. Also, Lyme mimics these illnesses, see my lyme thread below from my LDN

site. Also, get checked for Syndrom(sticky blood), it mimics MS and

other diseases. Lesions can be seen on MRI with and Lyme.

The only way to know for sure if you have candida yeast

overgrowth is to get a urinary dysbiosis test (measures by-products

of yeast in the urine) - stool tests can often miss yeast, but

the urine will show it. This is part of the Organic

Acid Test (OAT) and is done by Metametrix, Great

Plains, and Genova Labs - it must be ordered by a

physician. The entire OAT (metametrix calls it

Organix) tells you what vitamins you are missing and

is a very good guage of your overall metabolic

process, including toxicities and deficiencies. The

dysbiosis part only measure the by-products of yeast

and bacteria, and does not cost as much as the full

test. This is one of the routine tests I get on all

children with autism, as they have many metabolic

disorders and most have yeast and bacteria and need to

be treated for this to help them improve their health.

Dr. Jaquelyn McCandless

SEE BELOW FOR MORE

Lyme mimics so many autoimmune system illnesses (Read 1,165 times)

http://ldn.proboards.com/index.cgi?board=links & action=display & thread=926

=====

>

> I started LDN about 1 1/2 years ago. I have RRMS, transverse myelitis,

Fibromyalgia and C.F.I.D.S. The first year was great. I had no relapses and had

more endurance and stamina. Then it felt as though it started wearing off. I

have new lesions. Since January I've had three relapses. I'm having one now.

I've been on 3.5 mg.

> I follow an anti-candida diet and MS diet. I take supplements, vitamins, fish

oil, evening primrose oil, etc. Any ideas? Dosage suggestions? I'm thinking of

starting Copaxone. I was hoping to not have to do injections anymore.

>

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