Home SEARCH What is Trisomy 13? About This Site Donate
Contact Us

  Embracing Life - One Moment at a TimeTM

LivingWithTrisomy13.org

Ironman for Kids - The Living with Trisomy 13 Community thanks Michael Hennessey for helping to raise awareness for Trisomy 13 and other related disorders. See Video & Details>

Photo Album & Videos
Living with Trisomy 13 - Patau's Syndrome

< Previous

Return to Main Album Page

Next >

 Kimberly Adrienne Miller

Click here to send an update or photos

Born: October 14 1987 

 

Trisomy 13 mosaic 25% - Naples, Florida (FL)
"These children are a blessing from God"

~Cindy Miller

 

Update May 16, 2008

I just wanted to do an update on Kimmie. Kimmie was on her way to receive an award at her high school and of course we were so proud of her of course.

She is doing great and will be turning 21 in October. This coming year will be her last year of school, that in it's self is scary seeing as we have no program that is offered after graduation. My fingers are crossed and maybe something will come up.

She just became an auntie for the 3rd time on April 2nd (my older daughter had a baby boy, Thelmo John who joins his sister Skyla and Kimmie's other nephew baby Gregory) This makes her very happy she just loves babies and she is so proud of "her babies".

We count every day we get to share with her a blessing and still sometimes take one day at a time. God bless all the families here and I even though I may not respond to all the emails I do read each & everyone of them.

Cindy & Tommy Miller Kimmie's proud parents.
cmiller0429@aol.com 


- - -

February 13, 2007

My name is Cindy Miller my husband Tom & I are the very proud parents of Kimberly Adrienne. Kimmie as we all call her was born on October 14 1987 and wasn't diagnosed until she was 7 1/2 weeks with Trisomy 13 mosaic 25%.

Having very little information on Trisomy 13, let alone the mosaicism our family took everything one day at a time.

Though the doctors weren't optimistic about her future we knew we would never give up. Kimmie was the youngest of our 3 children and the star of the family.

Kimmie now is 19 years old and though she has limited speech lets us know what she wants seeing as she understands everything LOL . She loves going to school and hanging with her family. Kimmie did have a tracheotomy in 1997 due to severe sleep apnea but other than that she is in pretty good health.

I would love to hear from other parents. These children are a blessing from God and it would be nice to hear from other families.

I have enclosed a few pictures of Kimmie. One of them is her helping her daddy to cook something she LOVES to do .

Thank you
Cindy Miller cmiller0429@aol.com 

 
 

 

 submitted: 2-13-07

 

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.)
 
 


 
 

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

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

Translation
Search Specific Languages or Countries

 

Design & Hosting lovingly provided by::
Apke Web Services