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Life with Short Gut Syndrome, Transplant, Brain Injury & a whole lot of adventure.

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I couldn’t pass this Captain America doll up. Patrick loved playing with him.

Posted on September 24, 2014 Full size 3264 × 2448

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Published inIslands of Adventure (Wish Trip Day 3)

Patrick’s COTA Campaign

Click here to for Patrick's COTA transplant campaign.

Hi! I’m Emily

In 2008 my husband Brian and I adopted an amazing little boy named Patrick. Patrick was born with Short Bowel Syndrome as a complication of gastroschisis. He received a liver-intestine transplant in 2014.

In addition to Short Gut, Patrick struggles with a brain injury, developmental delays, and food allergies. But in spite of all his challenges, Patrick faces life with excitement, happiness, and a twinkle in his eye.

This blog is about our journey together.

Find support

Short Gut Syndrome Family Support Group
Short Gut Support on Facebook
Short Bowel Syndrome Foundation
The Oley Foundation
Kids with Food Allergies

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Donate Life
Yes Utah

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