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Elijah's 4D @ 27 weeks
Morro Bay @ Christmas 2011
Our ENCEPHALOCELE BABY BOY,He Came into our lives to leave his footprint in our hearts and in a clay mold... WE NOW LOOK AT HIS CLAY FOOTPRINT AS A REMINDER, "WE MUST KEEP ON WALKING. OUR JOURNEY HAS'NT ENDED!" We will share our life here and how weve been forever changed by our SWEET 'Liji (Elijah Nathaniel Douglas)
OUR EMAIL
- mrsstevendouglas@gmail.com
"LOVE U FOREVER LIJAH"
I carried you in my belly for 9 months.
We held you in our arms for 25 hours and 30 minutes.
~We will cherish your life;
with every beating of our hearts~
Elijah was born on July 9th 2008. He was born with a condition called Occipital Encephalocele. A lethal condition where the brain has herniated through a tiny[or large] hole on the head which did not close during the first 25 days of formation within the womb.
We learned of this condition on February 13, 2008 [I was 16 weeks pregnant]. during a routine scheduled ultrasound.
We held you in our arms for 25 hours and 30 minutes.
~We will cherish your life;
with every beating of our hearts~
Elijah was born on July 9th 2008. He was born with a condition called Occipital Encephalocele. A lethal condition where the brain has herniated through a tiny[or large] hole on the head which did not close during the first 25 days of formation within the womb.
We learned of this condition on February 13, 2008 [I was 16 weeks pregnant]. during a routine scheduled ultrasound.
Elijah's 4D ultrasound @ 27 weeks
Elijah's 4D @ 27 weeks
BIG FRESNO FAIR
US still in Love, now more than ever
Morro Bay @ Christmas 2011
THREE LIL CUTIES
SO VERY BLESSED
About Me
- Steve+Marie Douglas
- Weve been married since March 5, 2005. We have Kayla(now14) who became my daughter at age 5, the day her Daddy and I got married. Our 1st born is Josiah(now 7). ELIJAH (would be 4) our baby who was born and lived for almost 2 days. Haliah is our 2 yr old. WE ARE LEARNING TO WALK THE JOURNEY SET BEFORE US, AS PARENTS TO A BABY IN HEAVEN. We love being asked about Elijah and we think of him most days and every Holiday too of course
Global Visitors
Hello, welcome back on line x I think of you guys often and hope you are well, Barb from Melbourne
ReplyDeleteIve joined a group called FACES OF LOSS FACES OF HOPE. Im going to start our local group soon. Hope to be able to start helping new families walking this journey.
ReplyDeleteReading a story there I found that a hospital in Texas who "DID" take and donate encephalocele babies organs. So I feel so ripped off and like I failed to do "the best for Elijah" so im trying to DEALL with that huge void I feel. Like "there acctualy was somthing more we could have done. "emotions, emotions. Why would thedrs tell me it wasnt done :(
Id like to post pics,but not sure if I can from my phone. We have a gorgeous picture of Haliah at the cemetry. Weve taught her to point to Elijahs picture when we say his name. ;)
I'm still here, of course, and thinking of you all and praying for you. I wrote a post on my blog about getting to meet you guys, in case you'd like to read it:
ReplyDeletehttp://drbristow.blogspot.com/2010/12/meeting-blog-friends.html
God bless!