Goodbye 2012 and hello 2013

Hi guys, how was your end of 2012?
i haven't blogged in a while, I've been either ill or busy.
2012 end wasn't great for me, just before Christmas i was in hospital and on iv's for 4 weeks. including 2 weeks on an Aminophylline, yet my lung function was still only up from 24% - 26% but i guess it's something. Oh, and if you read this and you've had a transplant or currently being referred  when you had bloods taken for it, how many where taken? i had 12 bottles and i couldn't walk for nearly 3 days after, my legs went to jelly and i couldn't talk or stop shaking. Well, my letter has been sent to Harefield to be referred and i'm due to have a CT scan and some other bits n bobs done this month.
Luckily though i came out for Christmas, although i felt ill all through Christmas, but i tried not to let it get me down,which was hard. Don't get me wrong Christmas was great, i had some lovely presents and managed to keep down my Christmas dinner, although i had taken 3 sickness tablets not long before. I hope you had a lovely and healthy Christmas.
New year was good to, i went to a house party/gathering which was really good, although i never do anything all day so i had some energy for the night, and luckily it was a house party so i could sit down, and although my chest was bad all night i made sure that i carried on like normal so nobody knew.
Now, it's 2013 and I'm currently trying to stay out of hospital, although a trip may do me good. I hate going in so close to each admission, that's my problem you see, and i bet many other CF's we hang on until we know we can't cope no more before we go visit the doctor for a bed on the ward and start ivs.
2013 i am going to try to be as healthy as possible and push myself to do more things.
Anyway, i hope you all have a lovely n healthy 2013