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Helping Kids Lead “Ordinary” Lives

No one appreciates the perseverance behind medical research more than Kari Foss, a member of Kentwood High School's volleyball team, who was diagnosed with cystic fibrosis at age 2.

Cystic fibrosis can take its toll in a number of ways.

Symptoms can include persistent coughing, shortness of breath, sinus infections, and poor weight gain — all caused by a defective gene that causes the body to produce abnormally thick mucous.

The mucous clogs not only the lungs, but also the pancreas, where it prevents enzymes from reaching the intestine to digest food.

"Cystic fibrosis sounds like such a terrible disease, but with all the research that's going on, people with CF can accomplish a lot in their lives," she says.

"I know it slows some people down, but I've never really had any respiratory problems and I've always been able to keep up with everybody else in sports. The biggest problem is dealing with all my treatments and the time it takes each day."

Kari has participated in four cystic fibrosis studies at Children's. Not only does she feel like she's helping future CF patients, she considers it payback for the care she's received at Children's Cystic Fibrosis Clinic.

Learn more about research at Children's.