Each morning, most of us rise, get dressed, and head to work or school with little thought. But for someone living with Cystic Fibrosis, the day begins very differently.
Before they can even leave the house, a child with CF often endures 30–45 minutes of exhausting chest physiotherapy, a physically draining routine just to breathe more comfortably. This is followed by a schedule filled with inhaled medications, digestive treatments, constant coughing, fatigue, and the looming risk of infection.
At Child Life Society, we understand the daily reality of living with CF. And we’re committed to lightening that burden. With carefully guided research, medical partnerships, and a network of generous supporters like you, we provide vital tools and services that help children and their families manage this condition with dignity, comfort, and hope.
Together, we can make every breath a little easier.