Having DBA has taught me to not give up the fight and to do the best that I can. The DBAF has become more than just a source of friends and knowledge, but a family of support through the bad and the good.
Kristin – 25 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.
Kellan – 22 months
Our son has truly changed our perspective on everything.
Liam – 5 months
Nobody is guaranteed tomorrow. Just because you have a warning doesn’t make you different than anyone else. It doesn’t make a difference in how you live each day.
Mike – 32 years, Alice – 4 years
Brian – 10 months
I am and always will be special. I am and always will be DBA Strong!
Corey & Tessa Ann – 27 years & 10 months
Living everyday to fight DBA
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.
Shelly – 48 years
Out of my way DBA!
Carlee Nina – 4 months
“In His hand is the life of every creature and the breath of all mankind.” ~ Job 12:10