Josh smiling

Meet Gabe

Both Little Gabe and his sister live with Cystic Fibrosis.

Our Dreamer apartment was home to 5-month-old Gabe and his family following his heart procedure.  Gabe and his 6-year-old sister Annie are both being treated for Cystic Fibrosis.  During a routine exam, Gabe was found to have a congenital heart defect called coarctation of the aorta, a narrowing of the large blood vessel that leads from the heart. He underwent corrective surgery at UVA Children’s hospital. 

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The Yellow Door Foundation can only continue providing critical support to families through generous donations.