My sister had lots made if you want one.
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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.
2 comments:
That's too cute! I'll ixnay my non-pink wearing policy for that! Go Beth!
I feel so bad poor Ellie. God bless her in all that she do and I hope that everyone buys a "Team Ellie bracelet!
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