Many people are not aware of how difficult it is for a child with a rare disease to live in Africa, as there is very little support out there for children with rare conditions. Olive is one of many brave and beautiful children who needs her community to help her.

Olive is currently 5 months old and tackling the challenge of DBA like a champion.  We are hoping to raise awareness through Olive as to the difficulties that children with DBA (and similar bone marrow failure syndromes) endure. We would love you to follow and support her through her journey.

By raising awareness for her foundation and the DBA Africa Registry, we hope to improve the lives of many children who need some good news every now and then.

Olive’s website is finally up and running. Click here to follow Olive