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Living with Trisomy 13 - Patau's Syndrome

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Logan James Raymond Lawler

Born: March 21, 2005

  Lancashire ,England - Partial Trisomy 13    
   
"Logan is a very special little boy, he has changed our lives, we see life very different now. Logan makes us so proud of all what he has achieved, he brings so much love into our home."

Logan is our 1st child. He was 15 days overdue, and was born by c-section. Logan was 10.7lb. When he was born, we noticed his right eye wasn’t open, and the midwife took him out the room very quickly, before I even got to hold him. When I did see Logan his head was very red and his eyes were all marked. Logan was 4 days old before we were told he had microphalmia of the right eye. As time went by we realized Logan wasn’t developing as he should, he feed well and put weight on, but he couldn’t sit up, or crawl. Logan was referred to a development centre and was diagnosed at 11 months that he had partial trisomy 13. Logan then had a lot of tests, he has 2 holes in his heart, 2 arachnoid cysts, an under development on the left part of his brain, he had no matter on his brain. Logan’s hypothalamus isn’t developed properly so Logan has growth hormone injections daily and regular checks on other hormone levels. Logan has never been a good sleeper, and is on phenegran to help him sleep. Logan has iron daily and wears a prosthetic lens.

Logan is a happy little boy, and is sociable, he is very active and never stops!!! Logan has been learning makaton since before he was 2, the Genetic Dr. told us it would be unlikely he would be able 2 talk like us, he may have a few words and sign or rely on sign. Logan is 4 years old now and he does have a few words and signs. Logan has behavioral issues and are being looked at over the next few months. Logan also is having tests due to having so many soiled nappies daily. Logan is developing nicely at his own pace. I have always done as many groups with Logan as suggested by all the professionals. Logan starts school in September 2009 with full time support. Logan started walking at 19 months, 5 days at 2 in the afternoon.

Logan is a very special little boy, he has changed our lives, we see life very different now. Logan makes us so proud of all what he has achieved, he brings so much love in 2 our home. It hasn’t been like we imagined having a child, but it has been a very special journey and it has brought us all closer together Logan is a very cheeky character.


Joanne and Glen Lawler
joannelawler@btinternet.com
 

  
 

 
 

 

Submitted 5-20-09

 

 
 


 
 

 

 

All text and graphics © 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.

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 (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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