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I have a disease called Cystic Fybrosis. A disease which effects your digestive system and lungs. Most CF(Cystic Fybrosis) patients have a nebuliser, which liquifies a medicine called colomicine, and he/she inhales it. And has to take tablets that help digest the food the patiens eat. He/she doesn't need it for fruit, vegetables or jelly sweets.
I had to have an operation when I was 4 days old. It was because I had an infection called "Macoliamilous". Their acess point was through my Appendix, which I had taken out by the Doctors.
I had another operation in 2006 to get rid of a MASSIVE(!) Kidny stone taken out. It was 1 and a half centimeters(I know it doesn't sound big, but it is for a kidny stone!)!
I had ANOTHER operatian in 2007. We decided to have a Port-a-cath(a silocan ball wrapped in some titaniam) fitted because every time we have to have introvenus medicine, we vould never get the lines in my arm! This is where the Port(port-a-cath) comes in. Instead of having to keep having the lines in, they go in the Port instead! How cool is that?!
My Doctor from my operation when I was born
This is me in Bristol Hospital after my kidny Operation
