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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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update on kaylee rose

October 19 2007 at 11:17 AM
  (Login miracles712)

 

i just have to say that i am very happy! kaylee has come a LONG way from just when she was 6months old. she is crawling, babbling, eating like there is no tomrrow. i couldnt be happier. she is in physical and speech therapy once a wk every wk. she is going to be starting special education next wk. i am so proud of her. i honestly dont know what i was so worried about. but now there is no stopping her. also her cardiologist will be taking her off her meds in jan. im so happy.

but i do have a question. if anyone out there has their child in special education, what kind of things do they do? i know every place is different, but im sure its the same all around. but was just wondering. hope everyone is doing well.

jenny & kaylee rose

 
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