“A heart transplant in 2007 brought me from my deepest, sickest day to feeling more alive than ever,” said Melissa Simon. “This new heart has given me a life I never imagined possible.”
When Melissa was 14, she was diagnosed with viral cardiomyopathy, a condition in which the heart becomes enlarged and weakened. For about a year Melissa was on bed rest and medications. In time her condition stabilized. “I learned to compensate for my decreased heart function and led a relatively normal life for many years,” she said. She finished her education, got married and started on her career.
When she was 26, an echocardiogram showed that one of Melissa’s heart valves was leaking. Doctors performed reparative surgery but Melissa’s condition worsened and she suffered from pressure on the heart that prevents it from functioning normally. “I went downhill fast,” Melissa explained. “Every day was a struggle.” Melissa was placed on the heart transplant list on May 20, 2007.
Fourteen-year-old Chloe Coleman died June 5, 2007 and the next day Melissa received her heart. “I am so grateful to Chloe for giving me her gift that represents the highest level of compassion for others,” Melissa said. “While her gift is my greatest joy, it’s at the expense of greatest sorrow for Chloe’s family.”
Melissa now has a close relationship with Chloe’s family and when she first did the 95-flight climb up the Hancock Building, Chloe’s parents were at the top to applaud. Also to honor Chloe, Melissa and her husband Dave named their daughter Chloe after the generous girl whose last act of giving was to donate her organs.
For more about Melissa, visit her website at http://www.MelissaSimon.org.