While I know the road will not always be without struggle, we will continue to learn more through research and the determination of the amazing DBA community.
Cole – 2 years
Audrey – 4 years
Living with DBA is the hardest, yet most fulfilling, aspect of our lives. Audrey is the absolute love of our lives and we are thankful everyday for her.
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.
Sarah – 33 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.
Alexandre – 9 months
Drew – 2 years
Good things come in small packages! I may be little, but I’m a fighter – DBA… no contest.
Mike – 32 years, Alice – 4 years
Katie – 3 years
Our little hero