At 22 weeks pregnant, I was sent to fetal medicine to confirm that my baby would be born with a congenital heart defect (Hypoplastic Left Heart Syndrome) Essentially, this is where one side of the heart is not functioning properly. At 5 days old, my sweet Paisley underwent her first open heart surgery (Norwood). At 5 months old, she had her second open heart surgery (Glenn) and then a few short days later, she had a g-tube inserted. She is now four years old and thriving. We are scheduled to have her final surgery in the summer of 2026. Without this organization and all of the research it helps bring, more of the babies born like my Paisley, would not have the chance of survival. Please donate what you can. No number is too small

#Paisley's Journey

#1in100

#CHD Warrior