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Re: DMPS/EDTA

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DMPS is different than DMSA.

Go ahead and try it.

If you have no real results after a year of chelation, think again

about whether mercury is the problem or something else. Unfortunatley

life isn't so simple as to let every autistic child have the same

problem.

> Dear Andy,

>

> I have been wanting to ask you some questions. We have been

chelating

> our son for a year and doing the 4 hour and 3 times a day

> supplements.

> We have seen NO improvment!!! We have however seen some in IV

> Glutione. We have checks his SULFUR he is fine alittle low but we

> give NAC. Would it be true a child might not beable to handle

> DMSA/ALA thur there GI track and in fact it could be making the lea

> in his intenises more irratated. (been on diet fo a year) He also is

> not showing no yeast. So why couldn't you try doing thur the blood

> in very tiny amounts. Would IVIG help this problem. What is the

> difference between DMPS and EDTA. My Companding told me he could

> make DMSA in IV form. Also my DOctor likes DMPS and wants me to try

> it orally in very tiny, 8 hour. Is DMPS different than DMSA. As you

> can tell we are very upset and wait to get him well.

> Thanks you (hope the spelling is good did not proof read)

> r

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