Hi all, this is my first post. I was diagnosed with PF approx 14months ago. At first I was doing really well, lung function and volumes good. Then last July I had slightly low SATs when walking so started using o2 when out and about. Come Nov, everything seemed to take a massive nose dive. Was told I needed a transplant, then told that because I was so bad that I no longer qualified. I have gone from being independent to totally dependent on my partner. I can still dress and feed myself but he provides all my meals, looks after the house, pets, laundry etc. I need a wheelchair when we go out and I am also on 24hr o2. This has come as a shock to me and I am struggling to cope mentally. I live in Spain and have not yet found a local support group, its good to know that you are all out there so at least I can have a moan occasionally. Bye for now.