LDN for ME/CFS

[Guest guest]

Hello ,

You asked :

>From: Prince <neutrino1@...>

>Subject: LDN for ME/CFS

>Is anyone using LDN for ME/CFS? :

I have RRMS (14y) and CFS (2.5y) and use 3mg (started

Apr 05) for both. No definite difference in either disease but

a small improvement in my energy level. I am also having

Cognitive Behavioural Therapy which could be helping.

Also it is worth researching Omega 3s and CFS (I take these

as well).

Good luck,

Mark

Oxford England

[Guest guest]

,

My first presciption of LDN is arriving today from Wellnes

Phamacy. My holistic doctor is supporting me on trying the med. for

CFS. It is the 4.5 level. I will let you know how it goes. I'm

personally looking for a change in my fatigue, hoping to regain some

ambition!!!

Question for MS members-------I started to have a vibration in my

body two years ago that is constant, like a low boil all over. Had

MRI and MS was deleted, BUT, I still wonder. I've done many therpys

for mercury removal since then, and it doesn't die down. Only time I

remember " it " subsiding was after some glutathione IV's. Input would

be welcomed.

God Bless,

Sara

> Is anyone using LDN for ME/CFS? If you are, what results are you

> getting? Thank you in advance for all replies.

> --

> My cat really loves me. When it is cold at night he lies right

> up against me in the bed to help keep me warm.

[Guest guest]

Hi -- Some people with CFDs have Lyme disease -- your partner could check it out at www.lymenet.org -- discussion site there under Flashdiscussion/Medical Questions. Also can do a search there for posts on CFDs. -- RobinSee what's free at AOL.com.