Because 10 years ago, we thought our CF program was strong, until we compared
ourselves to other children’s hospitals and realized just how far behind we were.
Because our program needed to get better – and only by learning from other
CF programs and being transparent with our patients’ families every day,
could we start building better protocols together.
WITH A MEAN LUNG FUNCTION
OF 97.4%,*
OUR OUTCOMES FOR
CYSTIC FIBROSIS ARE AMONG THE
BEST IN THE COUNTRY.
Because to save a child,
we have to keep asking questions like one.
*
Source: National Cystic Fibrosis Foundation Patient Registry Report, ages 6-17 as of 2011, the most recent data available.
