At ten years old, Jahliah Parker likes to have fun with her siblings, play on her Nintendo Switch, and, along with thousands of other children across the country during the COVID-19 pandemic and lockdown, is ready to go back to in-person school. She is the youngest girl of six children; her brother, whom she is close to, is the youngest in the family, and none of them do anything without the others. Much like her siblings, she is an ordinary kid except for one little thing, her congenital heart condition. Throughout her entire life, Jahliah has had to deal with erratic heart rhythms, skipping of her heart, heart beating too fast, sometimes to the point of pain, and asthma. At the age of nine, she started to have fainting spells.
Tag: Congenital Heart Defect
Kosovo: a country left to rebuild after crisis. Most affected are those who have the least control. At times, this can leave some of the most vulnerable, such as children with congenital heart disease, with few options for survival. In the wake of rebuilding a country, resources and necessary infrastructure to perform such life-saving interventions … Continued
Suzi Leahy was told her son Jett had little chance of survival. He was born with a congenital heart defect that ultimately required a heart transplant before the age of one. Suzi, her family, and the team at the NC Children’s Heart Center at UNC Children’s Hospital fought for Jett’s life.