cystic fibrosis is something i know a lot about. i was diagnosed at 4 weeks old and i’m now 23. i have lost many friends to the disease and have more struggling. this is for them and also for me. i’m not someone who enjoys exercise so the prospect of hiking 20km with pen y fan being a part of it is honestly kind of scary. i plan on training as much as possible to get ready for this adventure. i’m lucky to have some very good friends doing this with me who i will forever be grateful for. doing great strides has been on my bucket list for quite some time now, it’s time to tick it off. june 3rd 2023 let’s go!!!

Cystic Fibrosis Trust is the charity uniting people to stop cystic fibrosis (CF). We fund vital research, improve care, speak out and race towards effective treatments for all. Cystic Fibrosis Trust is here to make sure everyone with cystic fibrosis can live without limits.Since 1964, we've supported people with cystic fibrosis to live longer, healthier lives - and we wont stop until everyone can live without limits imposed by CF.