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Payton Grant Ferguson |
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Aug 8, 2008 - Sept 4th, 2008. |
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Bay Minette, Alabma (AL) - Partial Trisomy 13 with a Trans-location of 17 |
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 Our
son's name is Payton Grant Ferguson, he was born Aug 8,2 008 and he was called
home to God on Sept 4th, 2008. Payton had partial trisomy 13 with a
trans-location of 17.
He was born with many abnormalities but you couldn't tell him that. He fought
for every breath he took. We were so blessed to have such a wonderful gift from
God. Payton has moved our hearts in ways we didn't think were possible and in
the short amount of time he was here he taught us more in that time then I think
I will learn in the rest of my life time.
We will be forever grateful for having him be apart of our lives. We hope the
story of his life will reach out to others and help them see that these children
are worth a chance. Payton’s story can be read at
Mercymedical.com the (2008 winter edu)
The thing to remember about trisomy children is not to worry with the things
they can not do or how they will die but how they will get to live. "The
significance of a life is not measured by its length."
Thank you,
Niki and Ryan Ferguson and our other son Ethan (age 4 1/2)
rferguson96@att.net |
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Submitted 5-27-09 |
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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
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LivingWithTrisomy13.org 2005-2010 - all rights reserved
Use prohibited without permission
All information found on this site was submitted to
us directly by the families
and used on this site with their permission. |
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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.
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*Disclaimer
All material on this site reflects our personal journey with raising a Trisomy
13 (Patau Syndrome) - 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. |
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