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.
Pascal – 11 Years
Irelynn – 2 years
For Research, For Hope – Commited to helping find a cure for Diamond Blackfan Anemia – Give life, Donate blood.
Michael & Andrew – 13 years
Having twin boys with DBA makes you appreciate everything in life more on a daily basis.
Brian – 10 months
I am and always will be special. I am and always will be DBA Strong!
Emmalynn – 3 years
Living with DBA has had its ups and downs, but with all the love and support we have gotten from our family and friends, we have been able to provide our daughter with the best life possible.
Brooke – 7 years
Katie – 3 years
Our little hero
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.
Ashlynn – 4 years
Of all the people on earth, the Lord your God has chosen you to be his own special treasure. -Deuteronomy 7:6
Abby – 6 years
DBA is a part of who I am… it does not define me nor will it stand in the way of my hopes and dreams.