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Living with Trisomy 13 - Patau's Syndrome

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 Alissa Corazzini

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Born: September 3, 1992  

   Torrance, California (CA) partial trisomy 13/partial monosomy 14
 
"It's really amazing to sit back and just watch Alissa sometimes; she amazes me every day and is truly the happiest person I have ever met."

My name is Lisa Arturo Corazzini and I am the mother of Alissa Corazzini.

Alissa is 14 years old and has partial trisomy 13/partial monosomy 14.  At the time of her birth there was very little information available and no internet!  Alissa is doing exceptionally well.  She's in the 9th grade and loves to go to school; she especially loves to ride the bus.  

Alissa doesn't speak, but she understands everything and despite not being verbal (she does not sign either), she communicates better than a lot of people I know that are verbal.  It's really amazing to sit back and just watch her sometimes; she amazes me every day and is truly the happiest person I have ever met.
 
I've attached a few pictures of Alissa.  Unfortunately all the on-line pictures I have contain other family members in them (Uncle Josh and Nana are in these). I would love to be able to help someone deal with this new experience.   I know that when my daughter was born it was very difficult to find other mothers with tri-13 children and it took me a long time to come to terms with the wonderful challenge God has given me.  

If I can be of any help to others I would welcome the opportunity.
 
Lisa Arturo
lcorazzini@socal.rr.com


 

 

 submitted: 1-11-07

 

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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
15802 Springdale St.. #68
Huntington Beach, CA  92649

info@LivingWithTrisomy13.org

 

 

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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