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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:
Gib and Abbie, I'm so pleased to hear it.
I loved reading your posts, not because of the struggle, but because of the love in it all.
Gib, it is good to know you are doing well and have such a beautiful family and what sounds to be, doing good work, with Oceana.
onward and upward,
Tanya
san diego
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