Saul is almost four. He loves going to preschool and playing with his friends and learning with his teachers. When he is home, he wrestles with his two brothers, builds with blocks and legos, and listens and dances to music. He is a sweet and empathetic kid, ready to stand up for anyone who he thinks needs his help.
Saul was diagnosed after being in the NICU for two months after surgery due to CF. You can’t tell he is sick, but if he doesn’t take medication to help him digest his food and do an hour plus of breathing treatments per day, he would end up back in the hospital.
One of Saul’s CF mutations is very rare. He is dependent on comprehensive research that will make sure that therapies and drugs developed will be able to help him, too. Saul’s smile lights up a whole room and his sense of humor and ability to enjoy his life raises up everyone around him. We fight for him so that he can continue to experience the joy he finds in life and the joy he brings to others.
Join our team and support Saul and all who are living with CF.