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Living with Trisomy 13 - Patau's Syndrome

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Evan Cotter

Click here to send an update or photos

Born: May 11 2006 

 

Speonk, New York (NY) - Full Trisomy 13

2-12-08

I JUST WANTED TO POST SOME MORE PICTURES OF EVAN.
HE LIKES TO HANG OUT WITH HIS BIG BROTHER AND SISTER.
WE ARE WORKING ON HIS SITTING AND HE LOVES TO DRIVE HIS CAR (WALKER) IN REVERSE.
WITH HIS PMV ON HE IS VERY VOCAL AND HE ALSO SIGNALS YES, NO AND ROCKS HIS HAND WHEN HE WANTS TO SWING.
PLEASE ENJOY THE PICTURES AND DON'T HESITATE TO CONTACT US WITH ANY QUESTIONS
 
MARK 


Update

- - - -

Update 8-20-07
EVAN IS DOING GREAT.  I JUST WANTED TO UPDATE WITH SOME PICTURES

 

Update 1-17-07
Evan is home and doing very well.
He just turned 8 months on Jan 11th ( 6 Months corrected )
He smiles and laughs all the time

- - -

Evan Cotter of Speonk, New York (NY) was born on May 11 2006

My wife's name is Adrienne Cotter and we have three children Marc 10, Brooke 6 and Evan

Evan has full Trisomy 13 and has had the following surgeries
May 12 Meckel's diverticulum repair
June 1 Gastrostomy tube placement
June 8 Bilateral inguinal hernia repair
June 10 Tracheostomy
September 25 Fundoplication

Evan was born 7 weeks early at 4 lbs 9 oz and today he weighed 13lbs.  He continues to thrive getting stronger every day
Before surgery today he was wide awake and alert.  The surgery went very well and he is recovering in the NICU

PS Thank you for the strong support and prayers from the entire community who continue to support Evan and our goal to bring him home

God Bless
Mark

Update 9-27-06
Evan continues to recover in the NICU They were taken just before his surgery on Monday

God Bless
Mark

 

- - - -

 

9-23-06

He is doing well but still in the NICU
We are looking forward to bringing him home.
I will send you more information as time goes on


Mark Cotter cotterlandscaping@msn.com



 


 

 

 submitted: 9-23-06

 

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

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