Tartan senior Erika Nolby had a promising start to her track career as a distance runner, finishing sixth in the 3,200-meter race at the state meet in 2011 as a seventh-grader, then returning to state in the 1,600 as an eighth-grader in 2013. She even broke Tartan's records at those distances.
"I joined track and I didn't have any goals or any expectations. I didn't even really know there was state until I got there," Nolby said. "It was super fun when I was younger because I was doing really good and I had a lot of accomplishments."
The success was cut short, however, in May of 2014, the end of her sophomore season. Nolby discovered she had a marker gene for a genetic heart condition. Known as arrhythmogenic right ventricular dysplasia (ARVD), the heart muscle of the right ventricle is replaced by fatty tissue, weakening the heart's ability to pump blood.
Before Nolby's testing for the marker gene, she had found out her dad, Mark, had the genetic disease and therefore could pass it on. Her brother, Seth, tested negative, but she tested positive for the gene, meaning the disease could come on at any time.
"It's a rare heart disease … and they don't really know that much about it," Mark Nolby said. "All they seem to really know is that excessive exercising can bring it on. … So they basically say they don't want you to do extreme stuff."
The diagnosis meant Erika Nolby would have to run cautiously and switch her focus from winning to protecting herself. Mark Nolby said his daughter went from running nine miles a day to restraining herself.
"She can't push herself to where she used to," Mark Nolby said. "And she's frustrated because she's used to running all the time, but she's had to learn to be a good leader without necessarily being the best runner. As parents, it was a little hard at first, but she's got her health and we want to keep it that way."
Tartan track coach Jim Boyle, who also coached Erika Nolby for six years on the cross-country team, said she's invested more into her captain's role on the team since the diagnosis.