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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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Thanks for all the support, you guys!

October 20 2005 at 11:13 PM

  (Login IviRae)

 

DJ is still in the hospital. He needs the oxygen. They finally figured out it was the adenovirus, apparently very common, though his reaction to it uncommon. We plan to stay at the hospital until after Hurricane Wilma, who is headed straight for us, passesa and we can go home. They might send him home on oxygen. We have a fmily support coordinator through the Early Steps program. She is gonna meet with me next week and help me figure out what I can do to keep my family thriving and surviving!

The saddest thing is, I haven't heard from my husband in almost a week. And when I did hear from him, he cared more about nightmares he's been having than his sick son. He is such a jerk! What, do I give of Loser Attractor Scent, or something?

At least I got DJ out of the deal! lol !

I'll keep you all posted, but if you don't hear from me next week, it's b/c the power has gone out!

thanks to you all, you really are a blessing!

Mandi,
mommy to DJ (David Jr.)
4/14/05, Trisomy 21

http://pg.photos.yahoo.com/ph/mommy2bri_dj/my_photos

 
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