Our Baby Thomas: My Postcard from Heaven

Thursday, February 11, 2010

My Postcard from Heaven

5 comments:

MaryFebruary 12, 2010 at 2:49 AM
This is so very sweet. Where did you get this?
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JulieFebruary 12, 2010 at 7:56 AM
This comment has been removed by the author.
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JulieFebruary 12, 2010 at 8:01 AM
Hi Mary, its a scrapbook page that I made on Scrapblog. Thank you for your compliment. I have done other pages too. Please go to the website and have a look. Here is the address to cut and paste into your browser. http://www.scrapblog.com/viewer/viewer.aspx?sbId=2507461
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birFebruary 13, 2010 at 11:40 PM
Julie - I have a little something to send you but can't find your email address anywhere. If you'd like to email me - birni@cybergal.com I'll try to send it over to you. x

www.allthelittleponies.blogspot.com
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JulieFebruary 14, 2010 at 1:30 PM
Hi Bir, I have sent my email address to you now, thanks for letting me know that my email is not easy to find. Hopefully it is rectified now.
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About this blog

Thanks for visiting my blog. These are my memory pages. Dedicated to the life of our baby Thomas who spent 4 1/2 months in the neonatal intensive care unit at the Royal Childrens Hospital in Melbourne, this collection of writing and pictures documents his life from his birth in October 2007 until he passed away in February 2008.
I have posted the emails that I wrote to family and friends and some of the photos that I took. Some of the poetry was written by me and some of it I have found in my bereavement travels.
Grief is not logical, I do not know where it will take me day by day, but I have found that it is better if I don't resist, it is better if I let it take me where it will.

Our Beautiful Baby Thomas

Thomas was born on 17th October 2007 and he died 135 days later on the 28th February 2008.
Thomas was born with Down Syndrome, Tracheal Osophageal Fistula and Osophageal Atresia, Tracheal Broncheo Malasia and Pulmonary Hypertension, he had a lot to fight.
On the night he was born Thomas was transferred to the Royal Childrens Hospital in Melbourne for surgery to repair his Osophageus, that is when the Pulmonary Hypertension was discovered and surgery had to be stopped. We waited 15 weeks in the Neonatal Intensive Care Unit until he was well enough to have the surgery again. But in the weeks following surgery the Pulmonary Hypertension became more and more severe, to the point that the doctors told us that there was nothing left to do.
Thomas died with me and his daddy and his brother and his nurse. We held him and talked to him, we watched him go, quietly he slipped away.
I will never be the same again.