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Hello,

I have followed this site for months (I don't like the word lurk!). We have

an appointment with Dr Goldberg in June and although I am nervous, I really

feel this theory makes the most sense. I would like to meet someone who has

seen Dr G and who lives sort of close to me in Madison, WI. I did meet a

group of parents in Illinois last year which was great but I know at least

one person () has moved away. My son is very mildly affected and I

am concerned about 'rocking the boat' so to speak. My husband has been very

interested in chelation which we all know can be risky - anyway he took our

son to see Dr Amy Holmes in Baton Rouge - her recomendation was to

leave well enough alone and probably not chelate (thank goodness). We are

awaiting some lab work but she said it would have to be really out of wack

to do anything about it. has many days that I feel he was given the

wrong diagnosis (PDD) but my husband reminds me of 1 1/2 years ago and

offers to run the video of the constant stim behavior and echolalia.

Anyone in southern Wisconsin who is seeing Dr G - or anyone with a child on

the higher function end who has had succes with the treatment? What we

have done is GFCF, sensory integration, PT/OT, play therapy, and lots of

love and attention.

Thanks for any help offered,

Anne in Wisconsin

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Dear Mark and Anne,

My son has been a patient with Dr. Goldberg for over five and a half years.

We live in in Crystal Lake, IL which is about 90 minutes from Madison. (I

graduated from UW.) Be happy to speak or meet with you regarding ANY

questions, concerns, fears etc you may have. We also will be seeing Dr.

Goldberg in June (June 28th). Let me know if you're interested in getting in

touch!

Pat Koltun

Any WI people out there

> Hello,

> I have followed this site for months (I don't like the word lurk!). We

have

> an appointment with Dr Goldberg in June and although I am nervous, I

really

> feel this theory makes the most sense. I would like to meet someone who

has

> seen Dr G and who lives sort of close to me in Madison, WI. I did meet a

> group of parents in Illinois last year which was great but I know at

least

> one person () has moved away. My son is very mildly affected and

I

> am concerned about 'rocking the boat' so to speak. My husband has been

very

> interested in chelation which we all know can be risky - anyway he took

our

> son to see Dr Amy Holmes in Baton Rouge - her recomendation was to

> leave well enough alone and probably not chelate (thank goodness). We are

> awaiting some lab work but she said it would have to be really out of wack

> to do anything about it. has many days that I feel he was given the

> wrong diagnosis (PDD) but my husband reminds me of 1 1/2 years ago and

> offers to run the video of the constant stim behavior and echolalia.

> Anyone in southern Wisconsin who is seeing Dr G - or anyone with a child

on

> the higher function end who has had succes with the treatment? What

we

> have done is GFCF, sensory integration, PT/OT, play therapy, and lots of

> love and attention.

> Thanks for any help offered,

> Anne in Wisconsin

>

>

>

>

> Responsibility for the content of this message lies strictly with

> the original author, and is not necessarily endorsed by or the

> opinion of the Research Institute.

>

>

>

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