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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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A few tips

January 11 2008 at 3:47 PM

  (Login aaronsmomvic)


Response to Ok, I'm going insane, pls tell me my child isn't the only one...

 

Aaron was/is king of selective hearing. I always thought it came attached to the male chromosome

what I do is get down in front of him and make eye contact and tell him what I want. I've done this for years. I don't have to do it all the time anymore, but if he's not listening, I still do it. As his speech got better, I made him repeat my request. She may be able to do that with some words or short phrases. That way you don't have to yell, you know they've heard you, and you know whether punishment is necessary or not. HTH

Vicki, mom to
Aaron, Jacob and Kaelin

"Nothing is so strong as gentleness. Nothing is so gentle as real strength."

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