Keep on Keepin’ On!
Anders – 5 years
Katie – 9 years
DBAF continue to search for a cure for all DBA.
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!
YouKai (Stephen) – 5 years
We are hopeful that a cure will be discovered soon so that our son doesn’t have to endure pokes and disruptions and can feel good all the time – isn’t that what every child deserves?
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.
Jack – 3 years
DBA has forever changed our lives, but we will persevere until we find a cure.
Carlee Nina – 4 months
“In His hand is the life of every creature and the breath of all mankind.” ~ Job 12:10
Samnang – 3 years
After finally getting the right diagnosis, Samnang is surviving and thriving in Cambodia.
Sam – 6 years
Future ribosomal protein researcher…he just doesn’t know it yet.