Thankfully, our sweet girl functions very well with a low blood count. We couldn’t feel more blessed. There is hope!

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.

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.

We are not the first to say this and we will not be the last, the DBAF has saved our child’s life. I cringe at the thought of what her care would be had we not met the DBAF.

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.

Some days are good, others not so good. Please help find a cure for our family.

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?

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.

Our little hero

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