RE: Another New Member - MS & LDN

[Guest guest]

I came off of Copaxone to go on LDN. Am doing fine. and glad to get rid of

the side effects with Copaxone. My neuro doesn't know that I am off of

copaxone yet.

I am sure that he won't be happy that I am off of the copaxone.

Wishing you the best.

Marie

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

From: " Iain Kerr " <kerrso74@...>

<low dose naltrexone >

Sent: Thursday, July 03, 2003 8:43 AM

Subject: [low dose naltrexone] Another New Member - MS & LDN

> Hi All,

>

> I'm another new member to the group.

> I heard about LDN and I am intrigued as to whether it would help me.

> I have MS, and have read many testimonies from people with remarkable

> stories.

> I am currently taking Beta Interferon but after reading all the good

things

> with LDN I think should I change??

>

> Has anyone else come off Interferon and started LDN?

>

> I think my GP would be supportive but I don't think my neurologist would

be

> as there hasn't been too many studies.

>

> Thanks in advance

>

> Iain

>

> _________________________________________________________________

> Find a cheaper internet access deal - choose one to suit you.

> http://www.msn.co.uk/internetaccess

>

>

>

>

[Guest guest]

Welcome Iain, Mabell,Jody,jposbo77357 & Hi all:

I also have taken myself OFF copaxone! I also fired my neuro because he

would NOT LISTEN to me about Prokarin, or LDN! Oh well, I may look for

another one in another city. Maybe not for awhile! I have been on LDN

for 2 mos. now. I feel great! I also have not had copaxone shot for over

2 mos. I will not go off LDN, or go back on copaxone! I am still using

Prokarin patch daily. My only " side effect " if you will, is some

stiffness in legs after lying down, or sitting for a while. My walking

is still pretty goofy! I still scissor sometimes when I walk. But oh

well! I will take these " side effects " anytime compared to a relapse. I

have been on 3mgs. All along. I don't know if I will go up in dosage at

all I will check with doc later this mo. I sleep very well, and have

great energy. I wish we could tell the world about LDN! The word is

getting out. I hope you all get on LDN very soon. The best of luck to

you Iain, Jody,jposbo77357 & Mabell.

Share a smile, make someone happy! :)

Warmest regards, Cydney

Ps: I hope I did not miss any NEWCOMERS! I MISSED SOME OF MY EMAILS.

Sorry if I did! It is purely

unintenially! I'll catch you later.

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

From: Iain Kerr [mailto:kerrso74@...]

Sent: Thursday, July 03, 2003 5:44 AM

low dose naltrexone

Subject: [low dose naltrexone] Another New Member - MS & LDN

Hi All,

I'm another new member to the group.

I heard about LDN and I am intrigued as to whether it would help me. I

have MS, and have read many testimonies from people with remarkable

stories.

I am currently taking Beta Interferon but after reading all the good

things

with LDN I think should I change??

Has anyone else come off Interferon and started LDN?

I think my GP would be supportive but I don't think my neurologist would

be

as there hasn't been too many studies.

Thanks in advance

Iain

_________________________________________________________________

Find a cheaper internet access deal - choose one to suit you.

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