Re: Anyone has LDN for FMS?

[Guest guest]

I was diagnosed with FMS about 15 years ago. I had very severe symptoms. I have been taking LDN for 8 months and for me it has been a miracle. I started out at 3mg after a month I went to 4mg. I take my pill at bed time and within 5 minutes I am sound asleep, and sleep most of the night. Before LDN I did not sleep at all. If you want to talk some more here is my personal address, jbentley@...

-- [low dose naltrexone] Anyone has LDN for FMS?

Hello everyone,

I am new here and I suffer from fibromyalgia. I was told about LDN and read about how it

can and has helped a few people with FMS but I haven't actually had any exchanges with

these people. I am going to speak to my GP about it tomorrow and ask if I can try it.

I would like to hear from FMS sufferers like myself who were given LDN and find out how it

helped them, whether they had trouble having it prescribed.

Thanks!

Sabby

[Guest guest]

I have CFS and FM , my FM has gone away within the 3 months on it.

The CFS remains, though I believe it is going away though very

slowly.

LDN is a miracle. make sure u take the protocol exactly right.

> Hello everyone,

>

> I am new here and I suffer from fibromyalgia. I was told about LDN

and read about how it

> can and has helped a few people with FMS but I haven't actually

had any exchanges with

> these people. I am going to speak to my GP about it tomorrow and

ask if I can try it.

>

> I would like to hear from FMS sufferers like myself who were given

LDN and find out how it

> helped them, whether they had trouble having it prescribed.

>

> Thanks!

>

> Sabby

[Guest guest]

Hi Sabby

I'm Sylvia. Please keep me on your list of people with fibromyalgia.

Over none years, I've tried dozens of things, all of which have helped

temporarily only. I am very interested if this med is working for

others with this condition. Wonder if there is a way to have a list of

just people with fibromyalgia?

Thanks

Sylvia

On Sep 15, 2005, at 6:30 AM, HRH Sabby wrote:

> Hello everyone,

>

> I am new here and I suffer from fibromyalgia. I was told about LDN

> and read about how it

> can and has helped a few people with FMS but I haven't actually had

> any exchanges with

> these people. I am going to speak to my GP about it tomorrow and ask

> if I can try it.

>

> I would like to hear from FMS sufferers like myself who were given

> LDN and find out how it

> helped them, whether they had trouble having it prescribed.

>

> Thanks!

>

> Sabby

>

>

>

>

>

[Guest guest]

Hello Sylvia,

I do not have a list for people with fibro, I suppose we could start an offshoot

group for

FMS sufferers! My doctor is still looking into the LDN thing for me and there is

not much

hope for me so far. I really want to try it as I hear better things about it!

Sabby

>

> > Hello everyone,

> >

> > I am new here and I suffer from fibromyalgia. I was told about LDN

> > and read about how it

> > can and has helped a few people with FMS but I haven't actually had

> > any exchanges with

> > these people. I am going to speak to my GP about it tomorrow and ask

> > if I can try it.

> >

> > I would like to hear from FMS sufferers like myself who were given

> > LDN and find out how it

> > helped them, whether they had trouble having it prescribed.

> >

> > Thanks!

> >

> > Sabby

> > ▪