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.
Living with DBA is challenging and confusing at times but with the DBAF by your side their information and guidance is PRICELESS.
We hope for an easier life, until then we are grateful for each day together.
I am and always will be special. I am and always will be DBA Strong!
Though in our hearts we desire to be free from DBA, we have learned patience, love, trust, perseverance, compassion, courage, and to cry.
Thank you DBAF for being there for us as we continue on this journey.
The DBAF has been a life saver for us! They’ve supplied us with the knowledge and the resources to fight off anything DBA might throw at us.
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.
Lily loves everyday she has, especially the ones she’s not in the hospital. Lily is the strongest little girl I know, my hero.
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