Though in our hearts we desire to be free from DBA, we have learned patience, love, trust, perseverance, compassion, courage, and to cry.
Seth – 4 years
Maggie – 4 years
It’s not fun, but I am a tough cookie.
Brandy – 27 years
I stand DBA Strong with the help of my family, friends, and DBA friends.
Jack – 3 years
DBA has forever changed our lives, but we will persevere until we find a cure.
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.
Drew – 2 years
Good things come in small packages! I may be little, but I’m a fighter – DBA… no contest.
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.
Avari – 22 months
Thank you DBAF for being there for us as we continue on this journey.
Peyton – 6 years
I cheer for a cure for DBA!
Pascal – 11 Years
It has been seven years since DBA became part of our vocabulary. Our son’s diagnosis brought confusion, apprehension and despair. The discovery of DBAF is a stroke of serendipity. While even more tears were shed, these are now mingled with knowledge, understanding and, more significantly, hope. It will be through research that our son will be able to secure a brighter future.