Re: Progress Report...

[Guest guest]

In a message dated 5/11/2004 7:47:36 PM Eastern Standard Time,

theethers@... writes:

I don't like is the unmotivated feeling.

You said it! All I want to do is sit and veg out, or sleep. Yuck. Doc said

I can up to

20 mg (from 10 mg), if I felt I was leveling out, but I haven't decided what

to do yet. I sent an earlier post asking for opinions. Can't decide if the

unmotivated feeling is depression and need more meds, or that the meds haven't

full kicked in yet. (Starting week #4 tomorrow).

´¨¨)) -:¦:-

¸.·´ .·´¨¨))

((¸¸.·´ ..·´ -:¦:-

-:¦:- ((¸¸.·´*

[Guest guest]

Hi, Faiv.

Sorry you are having these yucky sides.

I'm on 10 mg, and the only thing I don't like is the unmotivated feeling.

Not good if you're a writer, and probably not for anything else either.

Strangely enough, the relief I got from the panic attacks when I first

started on 10 mg a couple months ago actually motivated me. That freedom was

so complete and unexpected that I went out swimming, walking, everything.

Now I guess it's built up in my system more or something, and I'm content to

sit. Well, almost content. LOL

Hope your sides diminish and you feel better soon.

Thea

Progress Report...

> Hi All,

> Have been on 5 mg lex for a couple months... still REALLY tired and

unambitious from it.

> That is why I have stayed @ 5 mg. It has helped with the anxiety a bit, i

take less xanax,

> but the tiredness is a constant for me. I have been on thid before, a year

ago and stopped

> because of this. I have much less headaches than before though. Still

easliy stressed and

> kinda spaced out on this shit.

> Has anyone stayed @ 5mg for a long period?

>

> Best to all,

> Faiv

>

>

>

>

>

>

[Guest guest]

---

Congratulations! It truly works!

Steve

In low dose naltrexone , " bigbaby42246 " <YUK713@a...>

wrote:

> First I want to say thank you to all the members, for

> all the info that this site gives to people like my

> husband and myself. Because of this group I told our

> Neuro Dr about LDN and he checked it out and at the

> next visit I asked him for a script for LDN 4.5 mg.

> My husband is the first MS patient that he gave it to.

> He has been on it for 4 1/2 weeks and yesterday he

> jumped off of his lounge chair and walked down the

> sidewalk looking like nothing was wrong with him. He

> almost always uses a cane or holds my hand. I am

> so greatful to Dr Bihari and this site.

> Big Hugs to You All!

> Donna

[Guest guest]

Congrats from Louisiana! I can't wait until I can jump off of

*anything*!

(MS)

Day 3

> > First I want to say thank you to all the members, for

> > all the info that this site gives to people like my

> > husband and myself. Because of this group I told our

> > Neuro Dr about LDN and he checked it out and at the

> > next visit I asked him for a script for LDN 4.5 mg.

> > My husband is the first MS patient that he gave it to.

> > He has been on it for 4 1/2 weeks and yesterday he

> > jumped off of his lounge chair and walked down the

> > sidewalk looking like nothing was wrong with him. He

> > almost always uses a cane or holds my hand. I am

> > so greatful to Dr Bihari and this site.

> > Big Hugs to You All!

> > Donna

[Guest guest]

Okay. Actually, the email addy I use for this group is one I use only for

groups, for the most part. I'll email you from my gmail account.

: )

Looking forward to chatting with ya!

~Lyd

www.sistersunshine.com

Re: the continuous hand-

holding -

> Eve's Attitude!

> >

> Hey Lydia, I agree the nurturing is very important. If it weren't

for

> the open arms extended to me when I first posted here, I don't

think

> I would have been confident during my challenge. I've made a few

> email buddies and phone pals.

--

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