Board members

Julia is the founder and president of the non-profit. She is a part of the Wake Forest University Class of 2029 on a pre-medicine track. Her goal is to raise as much awareness and money as possible for Cystic Fibrosis and the hospital her sister has spent a lot of time at. read more about her under the sisters perspective blog. 

Sara is the mother of Julia and Lyla. She is another one of the founders. She has spent many nights at the Children's National Hospital and has seen first hand the importance of finding a cure for Cystic Fibrosis. Sara enjoys taking Maggie (our team mascot and therapy dog) into the hospital for patients and families. 

John is the father to Julia and Lyla along with another founder. He has also spent many nights in the hospital and has worked alongside the hospital. He has seen first hand the hospital's need for support from outside sources and how patients are affected by daily changes. John enjoys doing speeches  at schools and other events with Lyla in order to raise more awareness for Cystic Fibrosis.