65 Roses?....A beautiful way of saying Cystic Fibrosis, however does not make CF any more beautiful. My wish is to be standing untarnished, unbreakable, breathing easily.... A blog that is about my day to day life, as well as trying to cope with my illness Cystic Fibrosis. There will be no hold backs just me...out in the open, hope you enjoy! xXx

Thursday 22 December 2011

What to say

I've not blogged in a few days, i am now home from hospital but continuing on iv's until Christmas eve.
I'm feeling very overwhelmed at the moment, my head is full of confusion over how things are with my health at the moment.
I will blog soon when my mind is clear enough to think how to put words together.
x

No comments:

Post a Comment