[SPAM] Re:low dose naltrexone for MS

[Guest guest]

I just wanted to say that you are all in charge of your own health.

Your neuro cannot MAKE you take anything you dont want to. Whoever

chooses just to take LDN should not be bullied into taking Copaxone

as well, unless they think they might benefit from it.

`s neuro originally tried to " persuade " (or bully!) him into

Avonex years ago and we refused saying we were planning on trying

LDN first and if he didnt give us a script then we`d find someone

who would. He kept trying for about a year after the initial LDN

script but changed his mind when he saw the results of the first

MRI! Any doctor that refuses to listen to you and forges ahead with

THEIR plan is not a good doctor. You need to make the decisions you

are happy with - after all, it`s your life not theirs.

> >

> > kyleigh150,

> > I've been taking LDN for about 4 years and my thinking seems

clearer,

> my

> > balance may be better and generally I feel better. I have not

had an

> > exacerbation during that time. I did stop taking Rebif, too

which

> could

> > account for all the improvement (I am not a big fan of the

Interferon

> > drugs). I take Copaxone and LDN the FDA approved MS drugs are no

> better

> > than Copaxone and it doesn't have the side-effects for me and

> Copaxone

> > is the only one that works with LDN).

> > Larry

> >

>