Our little hero
Sarah – 33 years
Avari – 22 months
Thank you DBAF for being there for us as we continue on this journey.
Katie – 9 years
DBAF continue to search for a cure for all DBA.
Ty – 16 years
It is the tough things I have gone through with DBA that has made me the man I am.
Kendra – 34 years
With out the DBAF I would not be connected to others that have Diamond Blackfan Anemia. The DBAF has saved my life by educating me on what I need to do to combat this rare illness.
Maddy – 17 years
Difficulties are meant to rouse, not discourage. The human spirit is to grow strong by conflict. – William E. Channing
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.
Bailey – 4 years
This DBA family is the greatest group of people that I never wanted to have to know, but blessed that I do. The support from the DBA Foundation is immeasurable.
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.
Maggie – 4 years
It’s not fun, but I am a tough cookie.