As many of you know, in February of 2018, my sweet niece Caroline was diagnosed with cystic fibrosis (CF). CF affects nearly every organ in Caroline's body, most notably the lungs, pancreas, and digestive system. CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. It makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure.
 

CF is progressive, meaning over time, the symptoms cause irreversible damage to the body. Caroline completes at least 50 minutes of airway clearance and takes multiple nebulized medications daily to clear the thick, sticky mucus that CF causes to build up in her lungs. In addition, she takes 26 pills every day to manage her CF. She is a FIGHTER!
 

Although we've made great progress in the treatment of CF symptoms and preventative care, there is still no cure, and too many people with CF die young. The reality is that CF has a life expectancy tied to the diagnosis, and it’s a fight we must win.
 

Every person born with cystic fibrosis is on a unique journey and experiences this disease differently. While progress has been made, a long road lies ahead. We need a cure so that everyone with CF has a chance to live a long, healthy life.
 

As a grateful Aunt to a CF Fighter, I am raising funds for the CF Foundation and specifically Caroline’s Dayton Great Strides team – Caroline’s Crew!
 

Will you join me in making a donation to support cystic fibrosis research in Caroline’s honor? Every donation makes a difference. Your contribution can advance the research and science needed to drive our shared dream forward – a cure for everyone with CF. Together, we can change the reality of CF and give those living with it a better future.
 

Thank you so much for your support!