Re: need encouragement- to

[Guest guest]

I tried DMPS for a while and I was able to tolerate a higher dose

(more than 2x, since 2x would effectively be the same dose since you

take it half as often), so i am guessing that means i was making

faster progress. it's also nice to be able to sleep through the

night (if you leave out the LA which probably isn't worth it). I

really liked it. i felt pretty good on it. it is very expensive,

though.

I also have very high antimony. i wonder if with mercury and

antimony it makes it so you don't consistently improve the way you

might if it was just mercury. like maybe the antimony won't go

anywhere until you get rid of a certain amount of mercury... who

knows...

> > >

> > > I have reached my year marker and am evaluating progress or

lack

> > > thereof. I realized in the beginning that I would be chelating

> for

> > a

> > > minimum of 2 years, but believed I would see some improvement

> after

> > a

> > > year on this protocol. I was able to talk to Dr Teitelbaum

> > personally

> > > this week & ask his opinion. He believes that metal toxicity is

> > only a

> > > piece of the puzzle and wants me to go to a CFS/Fibro clinic

for

> > > further investigation. I'm becoming more skeptical all the time

> > with so

> > > many claims that this or that will be the cure. I've been ill

for

> > 16+

> > > years and my hope for ever attaining health is diminishing

> rapidly.

> > > Unfortunately like most of you, my resources are limited, so I

> > can't

> > > run off to Mayo Clinic (like outsiders are constantly

> suggesting).

> > I

> > > haven't gone into any details here, but how do I know if I'm on

> the

> > > right track? Shouldn't I be seeing some progress at this point?

> > > Joy

> > >

> >

>