CF is short for Cystic Fibrosis, but little kids called it "sixty five roses". Part of my daily treatment is taking tablets every time I eat. I also spend up to one hour a day doing physio and have lots of time in hospital where I have to have lots of needles and pricks, but not all of it is bad.
I get to eat junk food like chips, chocolate and cheese all the time. I also get to meet nice people at hospital. I got to go to the Gold Coast when I was six, organised by Make-a-Wish. They understand how hard it is having to do so much treatment and it was good to go to the theme parks. I still had to do all my physio and take tablets, but it was still fun.
I will always have to take tablets and do nebs and physio to stay healthy because there isn't a cure for CF. Danica wants to grow up and be a medical scientist and find a cure for Cystic Fibrosis. I think she'll be able to do it.
Love from The Smarties and Mrs N