I took a short video today and posted it on YouTube to show how well she is doing after her surgery. She is doing very well and everyone is peased with her progress so far.
http://www.youtube.com/watch?v=GTl4AsaFV1o
The one strange thing for Abby and I is getting used to her cry in the days after she had a ventilator tube in her throat. It makes even the tiniest cry sound so sad.
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.
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