Thank you DBAF for being there for us as we continue on this journey.
Jim – 35 years old
Lily – 10 years
Lily loves everyday she has, especially the ones she’s not in the hospital. Lily is the strongest little girl I know, my hero.
Emmalynn – 3 years
Living with DBA has had its ups and downs, but with all the love and support we have gotten from our family and friends, we have been able to provide our daughter with the best life possible.
Carole – 16 years
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.
Dawson – 2 years
He’s living on borrowed blood and we take one day at a time.
Brian – 10 months
I am and always will be special. I am and always will be DBA Strong!
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.
Gabriel – 7 years
We hope for an easier life, until then we are grateful for each day together.
Lola – 5 years
“Out of difficulties grow miracles.” – Jean de La Breyere
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.