Posted on: June 12, 2013
With something so rare, our biggest fear was that our son would battle DBA alone, he never does. Thank you DBA Foundation!
News & Events
Caitlyn – 9 years
DBA has affected our lives in ways we could have never imagined. It has introduced us to the most amazing people – from the dedicated doctors to the wonderful families who are also dealing with DBA. They all exemplify the power of human spirit and are family.
Kristin – 25 years
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.
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.
Sam – 6 years
Future ribosomal protein researcher…he just doesn’t know it yet.
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?
Avari – 22 months
Thank you DBAF for being there for us as we continue on this journey.
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.
Jack – 3 years
DBA has forever changed our lives, but we will persevere until we find a cure.