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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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Maeve Update

September 22 2008 at 1:27 PM
  (Login ginnynmaeve)

 

We don't post much, but here is a little update...
Maeve just celebrated the big 2! She is whirlwind of trouble! She is running and climbing and getting into everything! She got a trampoline and is learning to jump - what were we thinking???
She loves to clean - vaccums, washes the front screen door windows, empties the dishwasher! She is finally learning to drink from a big girl cup, so no more bottles by Christmas - we hope!
She is starting a preschool program and loves playing with other kids! She is really doing great develop wise. She signs up a storm and talks gibberish!
We just had surgery #8 and will be planning for reconstructive surgery in the near future of her tear ducts and nasal passages. She is having heart problems again and GI issues, so we have been very busy with doctors. And she had scarlet fever that was misdiagnosised as Hand Foot & Mouth. Boy oh boy! We sure have fun at our house, huh?
Well,thanks for reading and letting us share! Hope everyone is doing great!
Ginny & Maeve



Gina - 33
Sean - 36
Maeve - 1 year old



 
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