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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.
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2006
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November
(17)
- Steps in the right direction
- Look, Gramma, long sleeves!!!
- Three steps in the continuum of Children's
- Hi!
- Three Days Post Op
- Happy Thanksgiving
- Getting better all the time
- Ah, morphine, sweet nectar of the opiate gods
- One handed, left-handed Juggling
- Surgery Update
- T-minus 48 hours
- Reactions to the WSJ Omegaven Story
- X Marks the spot
- Short Gut goes to the Street
- A Whole new set of tricks
- 7 Months Old Today
- Play Time
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November
(17)
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