Kristina Druckrey

My Cystic Fibrosis Story

Nearly 40,000 people in the United States have Cystic Fibrosis: a rare, progressive genetic disease that affects the lungs, pancreas, and other organs. As a 24 year old with CF, I hope that one day there will be a cure for Cystic Fibrosis to ensure we too get the chance to live a long, happy, & healthy life  

Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.

My goal is to raise awareness surrounding Cystic Fibrosis, fundraise to continue medical research, support others who also have CF, & honor those who have unfortunately lost their battle.

You can support me!
By supporting this event, you have the opportunity to be part of ending this disease and making CF stand for Cure Found