Anyone with MS?

[Guest guest]

Hi all!

I am on my second month's bottle of Naltrexone. I have also been

on Copaxone for 10 months. Anyone else taking another therapy?

(ABCR?) I am interested to know what other's experience has been like

since taking the Naltrexone. I feel that my quality of life is

improved. I sleep better and am not as down in the mouth about

things. I have had an unusual experience since taking the naltrexone.

I will have symptoms of MS that feel like an exacerbation coming on

(not like aggravated old lesions) for half a day then it disappears,

but something else will come in it's place. Has anyone else had this

happen? I feel like my MS is trying to act up but the Naltrexone is

keeping it at bay but it takes some time to catch up. My neuro

doesn't know much at all about it since there haven't been any

scientific studies published. I have asked that my dose of 3 mg be

increased to 4 mg on my next prescription. Does this sound familiar

to anyone else? I'm am anxious for other's experience.

All ears,

Tracie

[Guest guest]

> Hi all!

> I am on my second month's bottle of Naltrexone. I have also

been

> on Copaxone for 10 months. Anyone else taking another therapy?

> (ABCR?) I am interested to know what other's experience has been

like

> since taking the Naltrexone. I feel that my quality of life is

> improved. I sleep better and am not as down in the mouth about

> things. I have had an unusual experience since taking the

naltrexone.

> I will have symptoms of MS that feel like an exacerbation coming on

> (not like aggravated old lesions) for half a day then it

disappears,

> but something else will come in it's place. Has anyone else had

this

> happen? I feel like my MS is trying to act up but the Naltrexone is

> keeping it at bay but it takes some time to catch up. My neuro

> doesn't know much at all about it since there haven't been any

> scientific studies published. I have asked that my dose of 3 mg be

> increased to 4 mg on my next prescription. Does this sound familiar

> to anyone else? I'm am anxious for other's experience.

>

> All ears,

> Tracie

Hi Tracie,

I have MS & Transverse Myelitis (diagnosed November 2004) and just

got my LDN but have to wait to take it till the Vicodin is out of my

system. I was on Betaseron to begin with and ended up getting a

really bad infection in my right upper thigh from the injection and

have been dealing with it for 3 months so I have stopped the

Betaseron.. Here is a couple links you might be interested in looking

at....

http://www.thecompounder.com/diseaseawaste.html

www.crystalangel.org (My Website on MS and Transverse Myelitis)

Let me know what you think...

Thanks,

Crystal