Help Candace raise money

Lynnleigh Hammond was born on June 7, 2022. Shortly after birth, she was diagnosed with a genetic disorder called Noonan Syndrome. Soon after a routine surgery, Lynnleigh started showing signs of a rare complication called lymphatic malformation. This caused Lynnleigh’s body to swell to twice her normal weight. Lynnleigh fought this complication until we told her she didn’t have to fight anymore. She passed away on August 14, 2022. Please join us at the Pumpkin Run to help LeBonheur acquire equipment and to train medical staff to diagnose this complication early on and to help us carry on Lynnleigh’s Legacy.