I stand DBA Strong with the help of my family, friends, and DBA friends.
Brandy – 27 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.
Ashlynn – 4 years
Of all the people on earth, the Lord your God has chosen you to be his own special treasure. -Deuteronomy 7:6
David – 1 month(now 12 years)
This is David at 1 month old weighing almost 2 pounds. DBA changed our paths in life, but I will ALWAYS be there to hold his hand for he holds my heart.
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!
Drew – 2 years
Good things come in small packages! I may be little, but I’m a fighter – DBA… no contest.
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?
Jack – 3 years
DBA has forever changed our lives, but we will persevere until we find a cure.
Keegan – 2 years
We are not the first to say this and we will not be the last, the DBAF has saved our child’s life. I cringe at the thought of what her care would be had we not met the DBAF.
Anders – 5 years
Keep on Keepin’ On!