When Jillian was 7, she got a new kidney from someone who had recently died. It was a difficult operation, and she would need to consistently take medicine for the rest of her life.
But it was worth it. Jillian stayed healthy for years, and she was able to take guitar lessons and play basketball just like other kids.
Then, when Jillian was 14, her new kidney stopped working—and once again, she needed a transplant.
This time, though, doctors said the kidney had to come from a living donor, and that donor would have to have Jillian’s blood type.
No one in Jillian’s family was a perfect match, and doctors said it would be extremely difficult to find the right donor.
Jillian and her family were devastated. “We all cried,” she says. “I was really scared.”