Living everyday to fight DBA
Corey & Tessa Ann – 27 years & 10 months
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.
Nicholas – 18 years
DBA has taught us many things – Never give up – Be grateful for the strength to fight the fight and always cherish the arms we rest upon for support.
Sarah – 33 years
Peyton – 6 years
I cheer for a cure for DBA!
Gabriel – 7 years
We hope for an easier life, until then we are grateful for each day together.
Keegan – 2 years
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.
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.
YouKai (Stephen) – 5 years
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?
Ty – 16 years
It is the tough things I have gone through with DBA that has made me the man I am.