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what do males take for this as in pills

--- mbrookh <mbrookh@...> wrote:

---------------------------------

This recommendation for alpha lipioc acid concerns me.

ALA is a

potent chelator which according to some crosses the

blood brain

barrier readily-can transfer heavy metals in and out.

Any of us with

a mouthful of amalgam[silver/mercury] fillings should

never think

about this product until metal is removed from the

mouth. The toxic

mercury load would be overwhelming.

For general information re toxic metals please see

http://www.dartmouth.edu/~toxmetal/TX.shtml

Vaccine injured children have an amazing profile of

symptoms that

fit within the scope of heavy metal toxicity. One

group that

addresses this is:

/

The archives are packed with info.

A brief summary that lists the symptoms of mercury

poisoning is

found here:

http://www.vaccinationnews.com/DailyNews/July2001/AutismUniqueMercPoi

son.htm

Our daughter, now 21, spent years with the labels of

mr, pdd-nos,

seizure disorder of unspecified origin, immune

dysfunction, etc. She

had about 85% of the physical complaints that mercury

poisoning

causes. Chelation has greatly benefited her. ALA is

one of the

agents we use. She has NO dental amalgams.

ALA (alpha lipoic acid) at about 600 mgs per day and

Ester C to

> bowel tolerance daily for a month along with the

liver flush. I

would then

> maintain the Ester C at 4,000+ mgs per day past the

first month.

>>

> Regards,

>

>

>

> Bruce Guilmette, PhD

>

> Survive Cancer Foundation, Inc.

>

> <http://survivecancer.net> Http://survivecancer.net

>

> Therefore do not worry about tomorrow, for tomorrow

will worry

about itself.

> Each day has enough trouble of its own. Matt 6:34

(NIV)

>

>

>

> _____

>

> From: low dose naltrexone

> [mailto:low dose naltrexone ] On Behalf

Of Aristidis

> Sent: Monday, February 06, 2006 3:41 AM

> low dose naltrexone

> Subject: [low dose naltrexone] T-cells

>

>

>

> Hi every one

> I'm in the group for 15 months and I never come

across to the

matter

> of T-cells.

> Since I was diagnosed, I'm fighting to bring those

in to balance,

and

> use LDN for this purpose. Not seeing any mention of

this, I'm

> wondering if I do the right treatment. I'm having

tests for T-

cells

> every month, and I see no improvement. Any comment

will be

> helpful.

>

>

>

>

>

> _____

>

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