We are happy to share with you our DBA Family’s personal story. Please note the medical information may not be entirely accurate and should not be used for diagnosis or treatment options.
By Deborah L. Shelton. Chicago Tribune.
Lily loves everyday she has, especially the ones she’s not in the hospital. Lily is the strongest little girl I know, my hero.
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?
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.
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.
With something so rare, our biggest fear was that our son would battle DBA alone, he never does. Thank you DBA Foundation!
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.
I stand DBA Strong with the help of my family, friends, and DBA friends.
DBA has forever changed our lives, but we will persevere until we find a cure.
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