Fighting to make CF stand for Cure Found.
Help us raise money to fund research and treatments for Cystic Fibrosis.
Our Story
April 21st, 2022, my wife Madison and I were thrilled to welcome our latest family member - a beautiful baby girl - Murphy Patricia Doyle. Soon thereafter, we learned that Murphy was born with Cystic Fibrosis (CF). We are asking for assistance in fighting this inherited, life-threatening disorder and would like you to join the “Mighty Murphy” team in our 2nd annual golf event!
CF damages the lungs and digestive system and is a rare condition, with fewer than 1,000 cases per year. While there have been great medical advances in recent years, unfortunately there is currently no cure.
Our lives have been forever changed by this devastating news, but with the help of an amazing medical staff at Children's Hospital in Minneapolis, our "Mighty Murphy" is growing into a sweet, smiling, happy child, unphased by the constant fight against CF. The past two years have certainly been challenging, but we are steadfast in our commitment to do whatever we can to care for Murphy and support everyone affected by CF, until a cure is found.
We will continue the fight to make CF stand for Cure Found for everyone who is impacted by this disease.
Until it’s done.