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So far I have mostly chelated with DMPS because I have a huge problem

with remembering things in the daytime, and it was impossible to wake

at night and be alert enough to take pills. I chelated for almost 2

years, and during that time the DMPS definitely reduced body burden

because my hair test normalized, and I have been able to tolerate

increased doses of chelators.

I am much more severely poisoned than most, and the mercury must be in

critical locations because I have almost no normal adrenal function

left. I am only able to function because of hormone replacement. My

major exposures to mercury were huge, and mostly 30 years or so ago.

I also had some serious set backs (during the last 3 years) that I

think were more related to my poor adrenals than to chelation - heat

stroke, an infection, a colon problem, and pain (not sure what is

causing this pain). The pain is interfering with my ability to walk,

and that is driving me on because I cannot afford to lose any more

mobility.

I think that the only possible way that I will beat the pain that I am

in is with ALA chelation.

I have finally started ALA. (I had tried ALA for a few rounds at

various times in the past, with much difficulty). I am using a dose

of 12.5 mg, every 3 h, and I made it through the past 2 nights!! It

was a family effort - everyone helped out to wake me at various times.

The 3-4 AM dose was the most difficult - it took 3 alarm clocks plus

my son to pull it off. I learned that I need to sit up and drink a

full glass of water or else I will get some burning.

Now that I have started I want to keep going and chelate with ALA as

much as possible. It is like looking at a mountain that I have to

climb, and looking back at some hills that I already made it through.

It is so much more fun to scale mountains with the support of others,

and I am so thankful for everyone who has helped me along the way.

J

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