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.

Living everyday to fight DBA

Good things come in small packages! I may be little, but I’m a fighter – DBA… no contest.

I AM DBA STRONG…Take Charge of your DBA!

Donate blood and stem cells, save a life!!!

DBA is hard but it’s my child’s life. I have to teach him how to live life with it. I will advocate and help find a cure. The DBAF is helping us improve his life.

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.

With something so rare, our biggest fear was that our son would battle DBA alone, he never does. Thank you DBA Foundation!

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.

DBAF continue to search for a cure for all DBA.