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?
YouKai (Stephen) – 5 years
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!
Lane – 12 years
Same journey, different paths. Bound together by the same heartaches, triumphs, and hope for a cure. That’s DBA Family!
McKindree – 14 years
And when the storm is over, you won’t remember how you made it through or how you managed to survive. You won’t even be sure, in fact, whether the storm is really over. BUT…one thing is certain: When you come out of the storm, you won’t be the same person who walked in!
Alexandre – 9 months
Matteo – 2 years
Living with DBA teaches you to enjoy the moment.
Jack – 3 years
DBA has forever changed our lives, but we will persevere until we find a cure.
Natalie – 9 years
I am here. I am in the present tense. I’m not always here, and sometimes here is a very difficult place. Sometimes it is a labyrinth, or a Minotaur, or a rope I can neither let go of nor follow. It’s hard to find the right words, but I guess I would say that it’s something like feeling the floor. And that it is my privilege to feel it. -Meg Howrey
Hunter – 4 years
Donate blood and stem cells, save a life!!!
Shelly – 48 years
Out of my way DBA!