We live in Australia. My then 6 year old daughter was diagnosed with SAA in May 2015. Being so rare I was on the search for information, help and support. I read many blog entries and FB post form Shahonna she was a brilliant eloquent writer. The fact she survived so long on transfusions was amazing. It gave me hope that my daughter can make it through her hundreds of transfusions. We are now +100 days post BMT and she is doing well we just got home after 6 months in hospital. RIP lovely Shahonna your inspiration lives on.
