: Was Re: Stopping TD-DMPS

[Guest guest]

Hi ,

What I mean is that some kids have trouble with the TD part of the

chelator. Sometimes it is the carrier itself, sometimes it can be the

extras that might be added.

If you're using oral, then you don't have to worry that the problem

might be the TD part. Of course, you need to make sure that your oral

chelator (ALA would likely be the only one you need to worry about)

doesn't have fillers in the capsule. If you are using oral and your

child has problems, then you could be fairly certain that your child

is having trouble with the chelator itself, that is, if you have

eliminated all the other possibilities (too high of a dose, too

infrequent dosing, insufficient supping, etc).

Having said all that, the vast, vast majority of kids don't have any

problems with the chelators themselves, just improper protocols.

Is that a bit clearer? So much easier to explain all these things

face to face :-)

Keep asking questions. You want to be clear about all this before you

start :-)

Anita

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> Anita,

> I'm reading your post about AC protocol and learning alot. I am

going to go that route with my son and I'm trying to learn from you.

One of the things you said to Abid was " One of the reasons Andy

recommends oral over TD is that if you have problems you know it's not

something in the TD causing it " . Can you clarify this? Do you mean TD

never causes problems or you can't tell if it is or oral causes the

problems? Thanks,

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