cool new stuff
We went to the hospital today to pick up Ellis's external processor for his cochlear implant. It won't be activated it until next week. So we have a week to get used to it. I think he knows it's his cool new thing. Believe me, it's been on and off about a billion times today.
It felt so nice to be having an easy-going appointment after all the drama of late. We took the train in, had a short appointment, ate lunch outside, walked to the bookstore and browsed (I actually picked up a book on IEP's that looks like it'll be really helpful), got smoothies, and took the train home. Except for the part when we entered the hospital doors, and Ellis whimpered knowing where we were, I think he had a nice day, too. He has a great time riding the train and loved being out with his mommy and daddy.
And he and his daddy have a gleam in their eye because cool new stuff that involves batteries and wires has entered the home.
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Here's a book that I found most helpful about IEPs: From Emotions to Advocacy. www.wrightslaw.com :)
Posted by: Karen Putz | July 16, 2007 10:21 PM
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Thanks for the tip!
Posted by: Jeannette | July 17, 2007 08:00 AM
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Thanks very much for sharing so much of your journey with Ellis. I have really appreciated your honesty. In some ways I feel I have met you; due, I think, to our shared friendship with Bryonie!
Posted by: Abigail | July 17, 2007 10:11 AM