Having twin boys with DBA makes you appreciate everything in life more on a daily basis.
Michael & Andrew – 13 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.
Maggie – 4 years
It’s not fun, but I am a tough cookie.
Dawson – 2 years
He’s living on borrowed blood and we take one day at a time.
David – 1 month(now 12 years)
This is David at 1 month old weighing almost 2 pounds. DBA changed our paths in life, but I will ALWAYS be there to hold his hand for he holds my heart.
Peyton – 6 years
I cheer for a cure for DBA!
Brian – 10 months
I am and always will be special. I am and always will be DBA Strong!
Dean – 11 years
DBA is hard but it’s my child’s life. I have to teach him how to live life with it. I will advocate and help find a cure. The DBAF is helping us improve his life.
Jack – 3 years
DBA has forever changed our lives, but we will persevere until we find a cure.
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.