Re: ELIO :) from (suny) Carol

[Guest guest]

God Bless You Carol,

This is exactly what I was looking for. A success

story! I think that once people try LDN and it works

out for them they don't bother coming back here. So

there are many people on the board that are having

problems with LDN.

That can be discouraging, but story like yours are

truly uplifting!

Thank You

Ciao

Carol

--- sunynbrite56@... wrote:

> 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

>

>

__________________________________________________________

Find your next car at http://autos..ca

[Guest guest]

Hi Elio,

I feel like I am a success story too from LDN. I never felt any outragious changes but I continuously feel healthy. I have been on LDN for 2 years 4months. I feel strong and my mind is bright and happy. I still walk with one bad leg but my muscle spasms have eased up. I have plenty of energy . I try to eat healthy. I am still aware that I have MS. I know my limitations. I feel that I will always stay on LDN until there is a cure. Thank God that I found LDN.

Marie

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

God Bless You Carol,This is exactly what I was looking for. A successstory! I think that once people try LDN and it worksout for them they don't bother coming back here. Sothere are many people on the board that are havingproblems with LDN.That can be discouraging, but story like yours aretruly uplifting!Thank YouCiaoCarol--- sunynbrite56@... wrote:> 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 > > __________________________________________________________ Find your next car at http://autos..ca

[Guest guest]

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