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I have been on DMSA/ALA 12.5mg for the entire year. I tried once to

raise the dosage but felt terrible, so I have stayed at the same

dosage. My question though is whether I should try DMPS? What

differences could I expect? The reason for DMSA is that I had high

lead & antimony too. I'm seeing my doc next week & maybe it might be

worth investigating.

Joy

> >

> > 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

> >

>

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