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We are a group of friends who have come together because we share the common bond of caring for someone who has Trisomy 21. We are here to share therapy tips, medical issues, laughs, accomplishments and yes, even frustrations. We embrace what Trisomy 21 has brought into our lives. We feel that it has taught us to appreciate the true meaning of life. We count our children as blessings! We will fiercely protect them and fight for their lives to be valued just as all other peoples' are. We share our pictures, our stories and our hearts here not only to provide friendship and support for each other, but also in the hopes that others will open their minds and their hearts to our unique children and, in turn, make a better world for everyone.
 

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Well, we have our IEP meeting next week...

March 29 2007 at 2:47 PM

Vicki aaron's mom  (Login aaronsmomvic)

 

this seems so early to do it. Usually they wait until about the last week of school. I'm wondering if they are going to give him ESY or something, becuase I know those are due very soon. He hasn't gotten it the last 2 years, so I wouldn't think they would this year. Anyway, I guess I need to start collecting my thoughts. I am curious to see if they have a plan set up for next year. I am hoping for another inclusion classroom setting like we had this year. It is next wednesday, so I'll update then.

Vicki and Aaron, 7 years old

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