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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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Anyone's child with av canal had mitral valve replacement..

August 1 2006 at 1:56 AM
Cindy  (Login ZacharysMom21304)
Hi as everyone may know Zachary is having a mitral valve replacement/repair on august 15th 2006 we are looking for some encouraging words from anyone who has experience with this type of surgery. Thanks for any and all information.

Cindy


 
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