Read stories from our members.
I was born on the 17th November 1974, I was slow to feed & a bit blue colour skin. So I was put into the ‘special care baby unit’ at my local hospital (Northampton) for a week then referred to Oxford (Radcliffe Infirmary) for further tests. Before …Read story
I am 28 and received a double lung transplant in September 2013. I was born with the hereditary condition Cystic Fibrosis. Cystic Fibrosis is a condition that mainly affects the lungs and digestive system. I managed to complete university with increa …Read story
I received a heart & lung transplant 23 years ago, due to suffering from Cystic Fibrosis. It all began when I was just 18 months old I was diagnosed with CF. My parents knew I had Cystic Fibrosis because my older sister Caroline who was seven year …Read story
I was diagnosed with LAM (lymphangioleiomyomatosis – a lung disease which causes muscle cells that line the lungs’ airways and blood vessels to multiply abnormally) six months after I got married in 2004, I was 39 and I had a lovely 18-month-old daught …Read story
I had double-lung transplant surgery in August 2013, at the age of 31, due to Cystic Fibrosis. My CF lungs had got me as far as they could, so I was placed on the transplant list and was fortunate enough to only wait for 3 months until surgery, with on …Read story
I am 34yrs old and received a double lung transplant in April 2013. I was born with Cystic Fibrosis and fortunately I had been quite well for most of my life. Despite never being very good at it I loved sports, joined the local basketball and jiu-jitsu …Read story