DBA has forever changed our lives, but we will persevere until we find a cure.
Jack – 3 years
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.
Jensen – 4 years
Living with DBA is challenging and confusing at times but with the DBAF by your side their information and guidance is PRICELESS.
Drew – 2 years
Good things come in small packages! I may be little, but I’m a fighter – DBA… no contest.
Matteo – 2 years
Living with DBA teaches you to enjoy the moment.
Gabriel – 7 years
We hope for an easier life, until then we are grateful for each day together.
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!
Jamie – 7 years
This is Jamie…Jamie is 7 years old, from the U.K… and he has DBA…. he’s brave, he’s strong, and above all, he’s always smiling.
Carlee Nina – 4 months
“In His hand is the life of every creature and the breath of all mankind.” ~ Job 12:10
Grace – 8 years
“We are only as strong as we are united, as weak as we are divided.” – JK Rowling
Please come together and help find a cure for DBA.