We are running this triathlon together in dedication to my sister, and Sarah's close friend, Abi, who was diagnosed with CF in 2018. We want to raise funds for ongoing research and support for those dealing with this disease. We will be releasing Abi's story month by month in the run up to June in order to raise awareness and gather donations. 

Cystic fibrosis (CF) is a life-limiting genetic condition affecting more than 10,000 people across the UK. It affects the lungs and digestive system and can cause chronic infections and reduced lung function. Currently, half of those with CF will not live past age 41.The Cystic Fibrosis Trust is fighting for a brighter future for people with CF and their families by funding cutting-edge research, driving up standards of care and supporting people with the condition and their loved ones every step of the way.

“The day I was diagnosed, I had this really strong sense that a bomb had just gone off, and the shock waves were heading straight for my family, my body, my future, unstoppable. It was like my whole life was under threat. Since that day, life has been a roller coaster, and a lot of the time I’ve really struggled to remember who I am and to be happy again. But my family and my partner have been my steady rocks, I don’t know how I’d cope without them. As we move further and further forward from that day in 2018, we find new ways to cope and to give something back. Thank you for being part of this, by reading this page, learning about CF and supporting Becci with her triathlon!”

- Abi Howse, my beautiful sister