Secretin, Chelation, Therapies...help

September 27, 2001

Thank you to all who replied with my question regarding secretin. I am

quite confused on what to do for my son and would love some advice from

those more experienced than myself. My son is 21 months old and first

diagnosed PDD at age 19 months, and then autistic about 3 weeks ago. He

attends an ABA based program 6 hours a week and will be going full time in

about a month. He is doing wonderfully there and learning so much. We went

gfcf about 2 and half months ago, he is seeing a DAN Dr. in Long Island.

The doc has done the allergy testing and also recommended that he take

Nuthera, TMG, Cod Liver oil, Magnesium, and a couple other vitamins and

minerals. Should all of these things be started at once? What can I expect

to see from this? He also set up an appointment for to have his

first dose of secretin next month. I am very nervous about this. From what

I have read, its very unclear. Seems that there is not a whole lot of

research, and that only some kids benefit from it, and the thing that gets

me the most is that IF any positve affects are seen, they only last 4-6

weeks?? What is the point of doing this and spending 500.00 per injection

for something that only lasts a month??? I have not read anything about

lasting affects, when the secretin leaves the body thats it until there is

more? Please correct me if I am wrong. Does anyone know of any child who

received secretin several years ago...were there any side effects, or any

positve things that lasted?? I do intend to call the doc and discuss all

this. It was very hard at the appt because my son was screaming due to all

the allergy testing needles and it was too long of a day to sit there and

ask all these questions. I guess what I would like to know is what I should

do for my son. I want the best for him and will do anything to help him,

including paying 500.00 a month for secretin for the rest of his life if it

would help. I just dont know what to do and I am confused. Also, this

chelation that I hear so much about...my son had blood tests for the metals

and all came back normal and he has never had the MMR, does this mean he is

not a candidate for the chelation? Any information on any of these subjects

is greatly appreciated. Thanks so much.

Toby in NY, Mom to 21 months

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