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Re: ALA Intolerance, Kai

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>

> Hi

> >My theory is that if one atom of mercury collides with my adrenals at

> >the end of a round - I'm a basket case.

>

> That seems to be the case with me, but why only on ALA?

Because ALA reaches deeper into tissues and into the brain than DMSA

and DMPS.

> I had wondered if I am allergic to ALA, but that is impossible isn't

it?

ALA occurs naturally in the body. I don't think your reaction is

allergy related. It happened two days after you stopped the round

didn't it? I think it is a stress reaction (chelation is stress). I

have big time stress reactions when I stop rounds - but as the dose is

lowered there is a dose at which the reaction won't happen.

>

> >My adrenals are shot. I am on full replacement cortisol.

> Do you believe they will ultimately recover?

>

I believe that full recovery is possible. It isn't just my adrenals

that aren't working properly - there has to be some hypothalmus and

pituitary involvement as well.

When I was first given the HC prescription I was cautioned that I

might not ever get off of it (and also that I wouldn't heal without

it). I won't be at all disappointed if I never get off of it - HC has

given me quality of life. I would really like to get to the point

where I have some ability to respond to stress - right now I have none.

>

> >Now I can tolerate 25 mg DMPS

> per dose and am chelating continuously (without breaks because

> stopping is too hard on me).

>

> mmmm, We can't obtain DMPS her. I wish we could.

>

I remember a post in autism mercury from a SA woman who was using TD

DMPS to chelate her child. I will search for that.

> >I went back and looked at your hair test. I wonder why the Na is so

> >high!! Could it be that you are losing Na like mad? Do you crave

> salt? and do you give yourself extra? I have had to give myself loads

> of extra salt in the last year.

>

> I like salt, but I don't crave salt. I will try taking more. I don't

know why the Na is so high.

> The hair test book says it does not reflect body burden. Still confused.

> Doesn't Aldosterone have some effect on Na? It retains Na and makes

you lose K?

Yes, I think that's what it does.

> I just assumed it was because my poor adrenals are also shot.

>

> >Read pages 98-99 of " Amalgam Illness " about Mg and K. I don't

> >understand exactly why but some adrenally deficient people lose Na and

> >retain K and others seem to lose both.

>

> Maybe if they can make aldosterone the don't lose Na. But if they

can't the do lose Na.

>

> >You may find that you need to increase amount and frequency of Mg

> >supplementation and/or follow Andy's suggestion of using supplementary

> >arginine, glutamine and taurine to heal the gut so that Mg absorption

> >improves.

> I do all this except arginine.

>

> >I don't know what quantities of supplements you are taking.

> >Relatively large quantities of Vit C and B vitamins are supposed to

> >help the adrenals. I have added extra B6, thiamine, B12 and folic

> >acid (on top of the B complex).

>

> Yes doing this do. Going to start an adrenal program that includes

licorice, very high doses of Biotin, Bioflavonoids, B5 and B6 and see

how I do.

>

> >I'm sure that we will be able to tolerate more ALA with time!

> Honestly, I'm petrified to try. It really renders me use-less and

dysfunctional.

Maybe the time is not right yet. Chelating with DMSA will continue to

decrease your body burden until you are ready for ALA. I can't do ALA

yet for several reasons (have to be able to function in the day, no

place to go at night away from all these people I live with to set a

bunch of alarms, not alert enough at night to trust myself, etc, etc).

Good Luck

> But at the same time I know it is the only thing that will cure me.

>

> Thanks and TK.

> Kai

>

>

>

>

>

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