Our son has truly changed our perspective on everything.
Jim – 35 years old
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.
Maggie – 4 years
It’s not fun, but I am a tough cookie.
Avari – 22 months
Thank you DBAF for being there for us as we continue on this journey.
Sam – 6 years
Future ribosomal protein researcher…he just doesn’t know it yet.
Carole – 16 years
Sometimes I feel like the odd one out, restricted by DBA. I just have to keep reminding myself that God wouldn’t bless me with this challenge if He didn’t think I could handle it. I don’t let DBA define me, I try to defy DBA.
Peyton – 6 years
I cheer for a cure for DBA!
Bailey – 4 years
This DBA family is the greatest group of people that I never wanted to have to know, but blessed that I do. The support from the DBA Foundation is immeasurable.
Gary & Zac – 30 years, 5 years
Some days are good, others not so good. Please help find a cure for our family.
Corey & Tessa Ann – 27 years & 10 months
Living everyday to fight DBA