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Angela Frances Ricker      

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 Born: October 8, 2004

 

Orford, New Hampshire (NH) - Full Trisomy 13

Name: Angela Frances Ricker
Parents: David and Melinda Ricker
Siblings: Karina (5) and Dylan (3) Ricker
Born: October 8, 2004
Where: At home in Orford, New Hampshire, U.S.A.

Update: July 30, 2007

Angela is doing well.  She has recently learned to crawl and is pulling herself up to a standing position on all kinds of stuff inside the house and out. 

The following two urls will provide more info and photos (even a video of her first time crawling).  She is even better at crawling now. Yikes, we need to child-proof the house again!
 

Angela has an additional new sibling! A sister. Erin. 6 months old. And Karina is now 7 and Dylan 5. But the parents. We're the same age as always. ;-)

http://www.dartmouth.edu/~ricker/
http://picasaweb.google.com/david.w.ricker

 

12-19-05

Hello, my wife and I have a daughter with Full Trisomy-13.
She was born at home on October 8, 2004 and was not expected to live beyond a few weeks or months.  Fourteen months old now and going strong with very little medical intervention, just plenty of love.

Her story can be found at:
http://www.dartmouth.edu/~ricker/main.htm

My wife's email and primary contact is:
mountain8@juno.com

David W. Ricker
Dartmouth College
37 Dewey Field Road
Hanover, NH 03755-3580
(603) 646-1065

submitted:: 12-19-05

 

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Living with Trisomy 13
Focused on prayerful support and gifts of love to those touched by a Trisomy 13 child.
Inspired By An Angel
Attn: LivingWithTrisomy13
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Huntington Beach, CA  92649

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Text and graphics © LivingWithTrisomy13.org 2005-2007 All information found on this site was submitted to us directly by the families and used on this site with their permission.
Cover photo of Pamela Sullivan & her precious daughter Maria, copyright Pamela Sullivan 2004, used with permission.
If We Hold On Together  Song Copyright 2002 by Patricia Welch, Ltd. All rights reserved.   Used with permission.
 
*Disclaimer
All material on this site reflects our personal journey with raising a Trisomy 13 child. It is not meant to replace any medical advise of a professional familiar with your specific condition. The personal journeys of any parents on this site are only their opinions and their own journey with having a Trisomy 13 child. You should consult with your own physician or other medical professional regarding the opinions or recommendations expressed within these pages as to your own child's symptoms and medical condition.
 

Looking for ALL families who’ve had a trisomy child of any number. Whether you terminated, miscarriage, had a stillbirth, live birth - living or deceased. Including adoptive and Foster parents. Please fill out the TRIS survey  to help update the medical literature and to improve the quality and availability of medical care. Tracking Rare Incidence Syndromes (TRIS)  Click here to add your information

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