Re: Re: ELIO :) from (suny) Carol

[Guest guest]

the answer is there have been many many people who remain undiagnosed. There is ms, possible ms or probable ms. Also, the diagnosis can vary from doctor to doctor. The positive is you have no lesions and should never with LDN. Kathy

[low dose naltrexone] Re: ELIO from (suny) Carol

Has anyone had an MRI for possible MS, and been told there are no signs, only to have it develop down the road??? I developed vibrations/tingling all over my body several years ago. I was doing chelation for high metals at the time. My MRI said no leisions, but I continue to wonder?? Does the vertigo come and go?, and how severe is it? I'd be "satisfied" to know I truely have CFS, but as I say, wonder if it's early stages of MS?? God Bless,Sara > Hi Elio,> I started LDN in Sept. of 2002. and I have to say, I am extremley grateful > for the wonderful response my body has had with it. I still have my days > here and there. Keeping my stress level down, diet, exercise, pacing myself > and keeping a Healthy mind are all part of my daily life. I have had a few > flair ups, (vertigo, numbness, tingling of hands, face and feet) but not once, > in the past 3 yrs. have I had a relapse. I have RRM MS. and relapses were > becoming an every 3 month event in my life prior to LDN, which were bad enough > to keep me bed-ridden for up to 6-8 weeks. My last MRI came back with > positive results as well....My doctor told me that my lesions were "healing" > themselves!> > My life was changed by LDN. I believe in it. And if it all changed > tomorrow, then I will always be grateful and forever feel Blessed for the 3 very > full years it has given me.> > "UNTIL THERE'S A CURE"> > Carol

[Guest guest]

Hello Sara,

I have had MS since I am 23 years and I am 51 now. I have no lesions that show up on an MRI. I am chronic progressive. I am a quadriplegic. I am not on LDN yet. I am toying with the idea of self-medicating. My doctors tell me that my lesions might be microscopic. They really don't know.

Good luck,Lee

[low dose naltrexone] Re: ELIO from (suny) Carol

Has anyone had an MRI for possible MS, and been told there are no signs, only to have it develop down the road??? I developed vibrations/tingling all over my body several years ago. I was doing chelation for high metals at the time. My MRI said no leisions, but I continue to wonder?? Does the vertigo come and go?, and how severe is it? I'd be "satisfied" to know I truely have CFS, but as I say, wonder if it's early stages of MS?? God Bless,Sara > Hi Elio,> I started LDN in Sept. of 2002. and I have to say, I am extremley grateful > for the wonderful response my body has had with it. I still have my days > here and there. Keeping my stress level down, diet, exercise, pacing myself > and keeping a Healthy mind are all part of my daily life. I have had a few > flair ups, (vertigo, numbness, tingling of hands, face and feet) but not once, > in the past 3 yrs. have I had a relapse. I have RRM MS. and relapses were > becoming an every 3 month event in my life prior to LDN, which were bad enough > to keep me bed-ridden for up to 6-8 weeks. My last MRI came back with > positive results as well....My doctor told me that my lesions were "healing" > themselves!> > My life was changed by LDN. I believe in it. And if it all changed > tomorrow, then I will always be grateful and forever feel Blessed for the 3 very > full years it has given me.> > "UNTIL THERE'S A CURE"> > Carol

[Guest guest]

I think you would have nothing to lose at this point

if you tried it. All it can do is help.

God Bless You

Elio

--- Lee G <Ltdnrg@...> wrote:

> Hello Sara,

>

> I have had MS since I am 23 years and I am 51 now.

> I have no lesions that show up on an MRI. I am

> chronic progressive. I am a quadriplegic. I am not

> on LDN yet. I am toying with the idea of

> self-medicating. My doctors tell me that my lesions

> might be microscopic. They really don't know.

>

> Good luck,

> Lee

> [low dose naltrexone] Re: ELIO from

> (suny) Carol

>

>

> Has anyone had an MRI for possible MS, and been

> told there are no

> signs, only to have it develop down the road???

> I developed

> vibrations/tingling all over my body several years

> ago. I was doing

> chelation for high metals at the time. My MRI

> said no leisions, but

> I continue to wonder?? Does the vertigo come and

> go?, and how

> severe is it? I'd be " satisfied " to know I

> truely have CFS, but as

> I say, wonder if it's early stages of MS??

>

> God Bless,

> Sara

>

>

>

>

>

>

>

> > Hi Elio,

> > I started LDN in Sept. of 2002. and I have to

> say, I am

> extremley grateful

> > for the wonderful response my body has had with

> it. I still have

> my days

> > here and there. Keeping my stress level down,

> diet, exercise,

> pacing myself

> > and keeping a Healthy mind are all part of my

> daily life. I have

> had a few

> > flair ups, (vertigo, numbness, tingling of

> hands, face and feet)

> but not once,

> > in the past 3 yrs. have I had a relapse. I

> have RRM MS. and

> relapses were

> > becoming an every 3 month event in my life

> prior to LDN, which

> were bad enough

> > to keep me bed-ridden for up to 6-8 weeks. My

> last MRI came back

> with

> > positive results as well....My doctor told me

> that my lesions

> were " healing "

> > themselves!

> >

> > My life was changed by LDN. I believe in it.

> And if it all

> changed

> > tomorrow, then I will always be grateful and

> forever feel Blessed

> for the 3 very

> > full years it has given me.

> >

> > " UNTIL THERE'S A CURE "

> >

> > Carol

>

>

>

>

>

[Guest guest]

Lee, just do the LDN. Don't give it much thought. Just do it. It is not even self-medicating. It is like taking one sixteenth of a commonly prescribed dosage. My doctor says "I don't think this will help you but it can't possibly hurt you, so I will prescribe it to you. I am doing well as far as I know today and that is the best anyone can hope for. What is there to think about? Don't let other people talk you out of trying something harmless that could change your life for the better.Blessings, Kathy

[low dose naltrexone] Re: ELIO from (suny) Carol

Has anyone had an MRI for possible MS, and been told there are no signs, only to have it develop down the road??? I developed vibrations/tingling all over my body several years ago. I was doing chelation for high metals at the time. My MRI said no leisions, but I continue to wonder?? Does the vertigo come and go?, and how severe is it? I'd be "satisfied" to know I truely have CFS, but as I say, wonder if it's early stages of MS?? God Bless,Sara > Hi Elio,> I started LDN in Sept. of 2002. and I have to say, I am extremley grateful > for the wonderful response my body has had with it. I still have my days > here and there. Keeping my stress level down, diet, exercise, pacing myself > and keeping a Healthy mind are all part of my daily life. I have had a few > flair ups, (vertigo, numbness, tingling of hands, face and feet) but not once, > in the past 3 yrs. have I had a relapse. I have RRM MS. and relapses were > becoming an every 3 month event in my life prior to LDN, which were bad enough > to keep me bed-ridden for up to 6-8 weeks. My last MRI came back with > positive results as well....My doctor told me that my lesions were "healing" > themselves!> > My life was changed by LDN. I believe in it. And if it all changed > tomorrow, then I will always be grateful and forever feel Blessed for the 3 very > full years it has given me.> > "UNTIL THERE'S A CURE"> > Carol

[Guest guest]

Hello Sara,

You make good sense. I'm going to do it. I will keep you posted.

Thanks again,Lee

[low dose naltrexone] Re: ELIO from (suny) Carol

Has anyone had an MRI for possible MS, and been told there are no signs, only to have it develop down the road??? I developed vibrations/tingling all over my body several years ago. I was doing chelation for high metals at the time. My MRI said no leisions, but I continue to wonder?? Does the vertigo come and go?, and how severe is it? I'd be "satisfied" to know I truely have CFS, but as I say, wonder if it's early stages of MS?? God Bless,Sara > Hi Elio,> I started LDN in Sept. of 2002. and I have to say, I am extremley grateful > for the wonderful response my body has had with it. I still have my days > here and there. Keeping my stress level down, diet, exercise, pacing myself > and keeping a Healthy mind are all part of my daily life. I have had a few > flair ups, (vertigo, numbness, tingling of hands, face and feet) but not once, > in the past 3 yrs. have I had a relapse. I have RRM MS. and relapses were > becoming an every 3 month event in my life prior to LDN, which were bad enough > to keep me bed-ridden for up to 6-8 weeks. My last MRI came back with > positive results as well....My doctor told me that my lesions were "healing" > themselves!> > My life was changed by LDN. I believe in it. And if it all changed > tomorrow, then I will always be grateful and forever feel Blessed for the 3 very > full years it has given me.> > "UNTIL THERE'S A CURE"> > Carol