Sarah – 33 years
Audrey – 4 years
Living with DBA is the hardest, yet most fulfilling, aspect of our lives. Audrey is the absolute love of our lives and we are thankful everyday for her.
Finn – 5 years
Abby – 6 years
DBA is a part of who I am… it does not define me nor will it stand in the way of my hopes and dreams.
Diana – 28 years
I will not let DBA define me, I will let it strengthen me.
Lane – 12 years
Same journey, different paths. Bound together by the same heartaches, triumphs, and hope for a cure. That’s DBA Family!
Kellan – 22 months
Our son has truly changed our perspective on everything.
Liam – 5 months
Nobody is guaranteed tomorrow. Just because you have a warning doesn’t make you different than anyone else. It doesn’t make a difference in how you live each day.
Nathaniel – 7 years
With something so rare, our biggest fear was that our son would battle DBA alone, he never does. Thank you DBA Foundation!
Lily – 10 years
Lily loves everyday she has, especially the ones she’s not in the hospital. Lily is the strongest little girl I know, my hero.