I stand DBA Strong with the help of my family, friends, and DBA friends.

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.

Of all the people on earth, the Lord your God has chosen you to be his own special treasure. -Deuteronomy 7:6

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.

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

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

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?

DBA has forever changed our lives, but we will persevere until we find a cure.

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.

Keep on Keepin’ On!