Olivia's day started later in the day than most of her days. She had her port accessed (you know how that goes), had labs (counts are good but we are watching them closely), radiation and then chemo. Overall an easy day but there were still tears.
The rest of the week is pretty easy with just radiation and consults. They will retake her labs on Thursday to determine if a transfusion is required but Olivia has convinced them to not access her port but to do a small butterfly needle to draw blood. Hopefully her levels will be good and no port accessing will be required...fingers and toes crossed!
We are making friends at the RMH and it's so fun to see Olivia interacting with kids that are experiencing the same things that she is going through. We've met two other families that also have rhabodmyosarcoma. A cancer none of us had ever heard of until our children's diagnosis but now we all know so much about.
Llama llama Momma Blogga