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?
With something so rare, our biggest fear was that our son would battle DBA alone, he never does. Thank you DBA Foundation!
Thank you DBAF for being there for us as we continue on this journey.
DBA has forever changed our lives, but we will persevere until we find a cure.
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.
Some days are good, others not so good. Please help find a cure for our family.
We hope for an easier life, until then we are grateful for each day together.
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.
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