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,

Our EI experience has been real good. They have a coordinator responsible

for ensuring we have all that we need. The parent to parent support person

calls once a month to say hello and has hooked us up with other families

that live close to us. She's the best. They offer a coffee hour support time

two different evenings a month (based on the age of your child with a

disability so you can relate to the other folks there).

One thing I might emphasize is for the EI team to ensure the parents are

understanding the process and goals of the assessments done by the PT/ST/OT.

When our had her initial assessment, since she had no problem sucking,

we did not have a ST assess her. I was told just a week ago that the EI team

should have done the assessment anyway - even though I was saying no. I was

uneducated and therefore should not have been the one saying my daughter did

not need ST at the time. I guess I'm saying that the EI team needs to be

sure and cover all bases because many parents are still not fully educated

on DS right after the baby is born - especially when you have triplets!

There's no time to sleep those first couple months, let alone read numerous

books on DS. We rely on the EI team for education as well.

is now 7 mos. and having her first " official " assessment by an ST on

Monday. Did anyone else wait this long? I don't know yet if she is even

behind or how far behind she is until the assessment is done. When did all

of you start ST with your children?

Kay Tiernan

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