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Biliary atresia, portal hypertension, and I did have hepatic pulmonary syndrome.
I was six weeks old.
Well at the time I dont know- I probably didnt know a thing. (hahaha) But my mum and dad have been honest with me from the start.
I cant really remember but I know my mum and dad have never kept secrets about my health condition from me.
I suppose it affects me as I have medicines to take and I cant do contact sports.
When I was diagnosed with liver disease I had to take a few medicines but then after my transplant last year they all changed I was taking medicines over 10 times a day (some the same and some different). They have gone down a lot now but I will be on Tacrolimus Mycophenolate forever (that's unless scientists find a better way to do things or maybe even a cure)
I go to kings college hospital in London for my main check ups but I also go to my local one as well. I go to London every 3 months and go to Derriford in between.
The good things about it is knowing about this charity, I mean without my liver disease I would never of known about them.
The odd time off schools isnt bad, but it can get annoying sometimes.
The bad things are missing loads of school (like when I had my transplant) and no contact sports (basketball was my fave and an ideal sport for someone of my height).
Just the fact that I have to generally be extra careful all of the time.
My message to other people with some sort of liver disease as me is live your life to the full! If youve had a transplant you should be out there having loads of fun because you have been given another chance in life so just enjoy it because even though life can be pretty tough sometimes you only live once so you might as well enjoy it!