Sorry for the focus. She moves too fast for the camera to catch up.
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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.
1 comment:
HA! She is too cute in that rain coat! My Mary is 21 months old today, and it's been months since I've gotten a good picture of her. She just doesn't stop moving.
Good luck tomorrow. Ellie's fans in CT are with her in spirit!
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