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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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Hi! Introduction.

March 15 2005 at 4:09 PM
  (Login chrfathOH)

 

I just found this board. I post some on Unomas and NADS. Not too regular on either.

Lets see, I am a SAHM to Wheatley(7) who is homeschooled. Veronica is 23 months old with Down syndrome. She was born with a complete AV canal which she had repaired at 3 months she just had a second repair of her cleft mitral valve at the Cleveland Clinic when she was 18mo. It has been a very trying time for us. Veronica is developmentally around 9-12m. She is a butt scooter, has two signs, one word(Mama), and is starting to pull up to stand. She has services through Early Intervention - ST & OT once a month to every three weeks. I am not to thrilled with having the interuptions and Veronica has shown me many times she will do things when she is ready not when I want.

Healthwise she is doing okay. She has moderate leakage in both valves and now her right atrium is enlarged. But we were able to cut back on her lasix. She is on the closely watched follow-up program - every 6m to the cardio.

I guess that is about it. We also plan to homeschool Veronica.

I look forward to meeting everyone here.

Christi
Wheatley(7) and Veronica(23m)

 
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