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>From: ILuvARose@...

>

>Please remove me from the list!!!!! I have tried before, but it has not

been

>done!

>

>Thankyou

>

>---------------------------

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  • 4 years later...

----- Original Message -----

From: Reg Kreil

low dose naltrexone

Sent: Thursday, November 04, 2004 3:12 PM

Subject: Re: [low dose naltrexone] Re: How many mser's happy with LDN results started years after diagnosis?

Joan do you think your nuero will listen to you now especially after the new findings on Copaxone are released?

I just feel so vindicated right now

Probably those results (the nonstopping of MSprogress) are why copax works along with LDN as it wasn't really doing anything anyway.

Reg.

-------Original Message-------

From: low dose naltrexone

Date: 11/04/04 11:31:13

low dose naltrexone

Subject: [low dose naltrexone] Re: How many mser's happy with LDN results started years after diagnosis?

Hi , RRMS here since 1985. I started taking copaxone 7 or 8 years ago. The only thing I got from it was atrophy at the injection site, and "knots" at the injection site making it impossible to inject. I never knew if it was really helping me as my MRI's have only been 2 since my diagnosis, which I still don't understand. Anyway, after researching LDN for almost 2 months, I decided to try it. I began on Sept. 29 of this year. My new birthday! LOL! The VERY next day I noticed amazing energy that I hadn't seen in close to 10 years! And I have energy every day now! Also, I noticed that the leg tremors that I got at night totally disappeared! They used to keep me up sometimes all night. Now, if I get them, as soon as I take LDN, they are gone within 5 minutes of taking it. It amazes me! I am also noticing a slow but gradual improvement in my bladder function and my balance as well. My neuro agreed to prescribe LDN for me after I threatened to get it elsewhere. He actually made me promise not to tell anyone he prescribed it for me! LOL! He never even looked at the info I had for him on LDN. Since taking LDN, I stopped taking the Copaxone, which my neuro doesn't know yet. He will not be pleased about that, but tough! All I can say is LDN has changed my life. I am now able to do things after work if I choose, something I haven't been able to do in years. I was always too tired. I can't wait to go back to my neuro and tell him how great LDN is working for me. Maybe, just maybe, he will look further into it. Although I doubt it. All I can say is ife restarted for me when I started taking LDN and I plan on taking it for as long as I can! :-) Joan

____________________________________________________ IncrediMail - Email has finally evolved - Click Here

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  • 4 months later...
Guest guest

Oh, sorry guys. Brain fog I guess -- I forgot to look at where P.

Dalton's message was coming from since it was in my IN box, not the

box for this list. Now how did it get there? Don't remove me from this

list! I'm staying! The message I replied to had removal directions,

which obviously didn't work.

- Kate D.

On Wednesday, March 16, 2005, at 09:20 PM, Kate wrote:

>

> On Wednesday, March 16, 2005, at 09:22 PM, P. Dalton wrote:

>

> <image.tiff>

>>

> <image.tiff>

> <image.tiff>

>>

>>

> <image.tiff>

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