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Sabina & Anatole© 1996, 97, 98, 99 all rights reserved
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Hi all;
I'm Jen, SAH mom to Sabina (age 5) Daisy (3.5), Anatole (2) and Agatha
(10 months). My DH is Joe and we live in rural Belgium, WI.
Sabina is our eldest child, and was born missing her left arm
below the elbow. This did come as a shock to us, but we'd read enough
human interest stories on amputees to know the missing limb wouldn't be
a hindrance to her physically. By the time she was 2 months old it
became apparent to us that she knew exactly exactly how to use her
little arm and felt no frustration. We decided to ignore the
conventional wisdom and did not have her fit with a prosthesis. Now
she's 5 years old, and we've never regretted our decision. Sabina has
always been very dexterous, and by the time she was 2.5 years old she
was able to change her little sister's diaper and her own! Sabina now is
very into crafts. She loves to color, paint, cut, glue, and has just
learned to sew. She even threads her own needles. The above activities
both baffle and bore her little sister Daisy, who has been known to look
wistfully at her hands and say, "I don't have a little arm. I just
have hands." Even though Daisy has two hands and Sabina has one, there is no question that Sabina is far more dexterous and agile than Daisy. When Daisy was born I had thought that perhaps she'd be able to help Sabina with activities that require two hands. However, we still haven't encountered such an activity. Anatole came to us from Korea when he was 5 months old. Though
we'd expressed a preference for a child with a missing limb, we never
thought we'd find one missing the exact same arm in the exact same
place! Initially Sabina was worried because Anatole does not have a
"pointer" (an extra inch Agatha is our youngest, and is breaking everyone else's record in learning to walk and stand alone. She's got two hands like her sister Daisy, but at this point does not know or care. When Sabina was born, our biggest worry was that her missing arm would hinder her socially. There have been times when another child (or grown-up!) was frightened by her missing limb, but these incidents have been few and far between. For the most part, people notice, are briefly taken aback, and then move on. When she was very young each outing that took us out of the house was difficult for me, because of my anticipation of the reactions of others. To those of you who've just had a baby with a limb difference, I promise you: this part gets easier and easier! Jen |
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![]() Husband Joe rounds out our family of six. For all those interested, I wrote a FAQ on amniotic banding which can be found at the I-CAN website. I look forward to reading everyone else's intros! Jen . |
Jen's FAQ on amniotic banding
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A very special
THANK YOU to Wyatt and Michelle who are the proud parents of Joe
(RBE) for donating the www.child-amputee.net domain and web space. Copyright © 2004
International Child Amputee Network
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