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Dr. Neubrander and Chelation protocols ( Please help answer my questions)

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Hi,

I am in the midst of filling out the " books " (LOL) of forms from Dr

N's office. One of them is the chelation informed consent/parents

choice of protocol used...I have pretty much signed the papers with

the intent of starting chelation again. (We did Andy's protocol with

no adverse side effects other than lack of sleep!) ) I spoke to

someone at the office before about using Andy's protocol with the

shots and they said they were open to it.

My questions are the following:

Now that I'm filling out the forms there does seem to be any choice

other than the three protocols that are mentioned. I know I can get

the dmsa and continue to do it according to the cutler protocol

without saying anything...But those of you who DO use the Cutler

protocol and see Dr N, do you mention to them?

Should I write it on the form or what? I would like to know how you

handled this situation?

I know I'm the parent and I know the final choice is mine. But I'm

just curious as to what others have done?

Also, those of you who have an HMO and are going to his office (which

is out of network) has he been open to having your child's ped order

the tests? My son's pediatrican actually mentioned about getting them

done through them to save us money?

WHAT DO YOU THINK?

Thanks

in NJ

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Andy's protocol for the shots, is to use oral first, and then if there is

improvement keep increasing the oral until you are giving so much it is

inconvenient and you are forced to give the shots.

[ ] Dr. Neubrander and Chelation protocols ( Please help

answer my questions)

Hi,

I am in the midst of filling out the " books " (LOL) of forms from Dr

N's office. One of them is the chelation informed consent/parents

choice of protocol used...I have pretty much signed the papers with

the intent of starting chelation again. (We did Andy's protocol with

no adverse side effects other than lack of sleep!) ) I spoke to

someone at the office before about using Andy's protocol with the

shots and they said they were open to it.

My questions are the following:

Now that I'm filling out the forms there does seem to be any choice

other than the three protocols that are mentioned. I know I can get

the dmsa and continue to do it according to the cutler protocol

without saying anything...But those of you who DO use the Cutler

protocol and see Dr N, do you mention to them?

Should I write it on the form or what? I would like to know how you

handled this situation?

I know I'm the parent and I know the final choice is mine. But I'm

just curious as to what others have done?

Also, those of you who have an HMO and are going to his office (which

is out of network) has he been open to having your child's ped order

the tests? My son's pediatrican actually mentioned about getting them

done through them to save us money?

WHAT DO YOU THINK?

Thanks

in NJ

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