At 3 months old, I was diagnosed with Cystic Fibrosis.

Back then, there wasn't much research or information around the condition. My mum had been told I would only make it to my 16th Birthday, as you can imagine, that was a very tough time for her. I spent weeks, even months in and out of hospital, I even spent a few Christmases in there.

As I got older, the condition didn't get any better, some of my friends lost their battle with CF. My lung function would drop and I would panic, not knowing if I my body could fight the infection. People with Cystic Fibrosis are not allowed to mix due to cross-contamination - So I would spend most days on my own.

After turning 18, I got diagnosed with CFRD (Cystic Fibrosis Related Diabetes) This was where my life changed even more.

Fast forward 13 years, the research and medication has come on leaps and bounds. CF Sufferers across the world have been given a new lease of life, All thanks to the never-ending research and work by the CF Trust.

I want to give back to the CF Trust, to thank them for their hard work and for giving us all hope. Thanks to their ever-evolving research, I now have a normal life expectancy.

We want CF to stand for Cure Found.

Cystic fibrosis (CF) is a life-shortening genetic condition that slowly destroys the lungs and digestive system. The Cystic Fibrosis Trust is the only UK-wide charity fighting for a life unlimited, when everyone living with CF can look forward to a long, healthy life. www.cysticfibrosis.org.uk