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 Rayana Nicole Johns

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Born: January , 6, 2006

  Waldorf, Maryland (MD)      
 


My name is Shaunna Johns. My daughter's name is Rayana Nicole Johns her date of birth is January , 6, 2006. She was diagnosed with Partial Trisomy 13. We live in Waldorf, Maryland. She was born in Clinton Maryland. 

Overall, Rayana is doing really well. No medical problems or procedures. She is developmentally delayed and is cognitively speaking at about 15 months. She is walking and climbing doing most of what 2 year olds do.

Her biggest struggle is communication. She babbles but no talking. She just learned to sign the word more.

We are so proud of all Rayana has accomplished and would like to give some positive support to other families struggling with these types of challenges.

Shaunna Johns
SNRJOHNS@aol.com



 

 

 

Submitted 12-1-07

 

Have a child living with Trisomy 13??  We would love to add your child to our Album.
Click here to send us their information. (Please note in the subject area if this is a Trisomy 13 photo as I do not open attachments unless I am aware of the sender.)

 

 

 
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Click here to download printable LivingWithTrisomy13.org "awareness cards."

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

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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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