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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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"Memory Keeper's Daughter"

October 17 2006 at 9:30 AM
  (Login jennifergg123)

 

Hello!

This is my very first post here and by way of introduction, I am mom to three boys, a seven year old and twin three year olds. My middle son was dx with Down syndrome at five days old. I write about him, and post photos of all my children at www.jennifergrafgroneberg.com, if you are interested in these things. I am fairly new to the Internet and still finding my way around, but I think it's wonderful!

The reason for this post is that over at downsyn.com there is a book club beginning, and the interesting thing about it is that this month's book, The Memory Keeper's Daughter, features a twin with Down syndrome, and the book's author, Kim Edwards, has agreed to login and answer questions, comments, etc. It's a little bit of an opportunity for us all and I wanted to share that info.

The discussion begins Oct 19 and runs until there are no more things to say...Kim will login sometime a few days after the discussion has begun, so you might check back every now and then if you are interested.

Thanks for the site, I look forward to exploring it. I think I already recognize a few children! Hooray, familiar faces!

And I look forward to getting to know more of the posters here!

 
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