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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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We are hoping to go

March 17 2008 at 1:33 AM		   (Login JamieandCorisMom)


Response to NDSC Conference in Boston July 11-13
 

Have hotel reservations...just haven't worked out details yet. My mom usually comes along to watch the kids but is having her knee replaced in June so we may have to take you up on helping provide some travel funds for Laurel

Don't worry about the banquet...we have been to 3 conventions now but never go to the banquet...we can all get together and celebrate Adam's birthday....sounds like much more fun! And the dances are a blast! The kids LOVE them!

Lisa, mom to Jamie, 6 years old (and an extra chromosome) and Miss Cori, 5.


 
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