This is Jamie…Jamie is 7 years old, from the U.K… and he has DBA…. he’s brave, he’s strong, and above all, he’s always smiling.

With something so rare, our biggest fear was that our son would battle DBA alone, he never does. Thank you DBA Foundation!

After finally getting the right diagnosis, Samnang is surviving and thriving in Cambodia.

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.

Having twin boys with DBA makes you appreciate everything in life more on a daily basis.

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.

Living with DBA is challenging and confusing at times but with the DBAF by your side their information and guidance is PRICELESS.

Of all the people on earth, the Lord your God has chosen you to be his own special treasure. -Deuteronomy 7:6

Good things come in small packages! I may be little, but I’m a fighter – DBA… no contest.

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.