She's back.
Nuf said.
Start feeds today and are loooking for the door late Friday.
Thursday, June 04, 2009
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This is the story of Eleanor Brogan who was born in April 2006. She was born missing 90% of her small bowel and 20% of her large bowel. This made her "Short Gut" or "short bowel", hence the name of the blog. Currently she is being treated by Children's Hospital Boston. She was the 23rd child to go on the new lipid for TPN, called Omegaven. Which has saved her liver, kept her off the transplant list and we believe saved her life.
5 comments:
You guys continue to inspire and amaze us all. Thank you for sharing your lives and strength with us. Go Ellie you are one amazing girl.
Love,
Dan, Steph, and Quinn
That's awesome news. I like pictures of Ellie in her house with her Mom, Dad and Gus!
wahoo ellie!!! We're so proud of you!!
Miranda uren
Abby's mommy
www.abbyuren.com
Yeehaw!! So happy to hear that! I hope to see you guys again soon :)
Fingers crossed!
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