We got creative this afternoon witht he camera and the computer to take some of those pictures that go into picture frames......Gib's hand and Eleanor's.
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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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June
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- New pictures and videos
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- Surgery Update number one
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June
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2 comments:
Very awesome pic! Definitely one for the scrapbook!
Love you guys,
HEather
Hi:
I was thinking for the last few days of the choices you two have made about the fish oil and/or the more advanced method. I think you have made the right choice. Given the situation, no choice is wonderful, but you've chosen what I would choose, and what Martha would choose in your circumstances. As always I'm feeling really proud of you both. Eleanor has the best parents in the world.
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