This blog was created to be the story of a special needs baby and her journey through life. Now it is the journey of her mother coming to terms with her loss.
Tuesday, October 17, 2006
Fixed
I have fixed the comments and posted some photos of Branston's birthday on his blog. Thanks to those who let me know the comments were not working.
1 comment:
Anonymous
said...
ì LOVE your site. It's because it's so real and alive and full of emotion and honesty. I know I will never fully understand your pain but I can only hope that life will give you more peace as time goes on. I think it's wonderful that you have given your gorgeous little girl her rightful place in the spotlight and as a result have made her immortal. I don't know you but I so wish I could hug your pain away. Much, much love Lou & Craig
I am Kendra's mom and I maintain 2 blogs, this profile appearing on both. Kendra was and is my little angel. She was born on 23 April 2005 and lived till 24 March 2006. She had Jacobson Syndrome which means that she had a piece of her 11th chromosome missing. Kendra's World is the blog of her life and thereafter. KIDS support group is the blog of the special needs support group which I joined because of her.
1 comment:
ì LOVE your site. It's because it's so real and alive and full of emotion and honesty. I know I will never fully understand your pain but I can only hope that life will give you more peace as time goes on. I think it's wonderful that you have given your gorgeous little girl her rightful place in the spotlight and as a result have made her immortal. I don't know you but I so wish I could hug your pain away. Much, much love Lou & Craig
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