Join us on sample date
As told by his mother, Jessica
We quickly discovered that the CF community is small but mighty. We also discovered that the CF Foundation is making huge strides in finding a cure. There is ongoing groundbreaking research, amazing treatments in development (Brax could potentially be on a modulator “miracle drug” when he’s 2 if it’s approved for younger kids!) and exciting advances on the horizon. We now know our future will be full of laughs, tears, joy and most importantly hope. Our prayers are that there will be a cure in Brax’s lifetime.
He has CF, but CF doesn’t have him. Join us in the fight for a cure.