Hi, everyone! For those who don’t know me, my name’s Kendall and I’m doing this skydive (despite being scared of heights and flying!) on 14th June 2025, for someone very special… my beautiful 1 year old niece, Lottie. This skydive is in her honour, to raise awareness for cystic fibrosis and to recognise the incredible strength these warriors show every single day, even though they look “well” on the outside.

Lottie was diagnosed with cystic fibrosis at just 17 days old. Since then, she’s taken everything in her stride and makes it all look easy, but behind that bright smile is a tough daily routine of treatments, physiotherapy, endless hospital visits/admission and multiple medications. She faces more in a day than many of us might in a lifetime, and she does it all with the brightest spirit. Her fiery soul and constant smile inspire everyone around her.

You can read more on Lottie’s story, shared by her mummy, Rachel, on the Cystic Fibrosis Trust website here:

https://www.cysticfibrosis.org.uk/news/i-dream-that-one-day-lottie-will-live-an-unrestricted-life

Thanks to life-changing medication, Lottie, like 90% of CF patients, is able to live a much-improved life. But sadly, approximately 10% of those with CF aren’t eligible for these life saving drugs for reasons such as having rare genetic mutations, intolerance of side effects, to name a few. That’s why I’m raising money for the Cystic Fibrosis Trust - to help fund vital research, support those affected and their families, to push for broader access to treatments, and help fight for a world where no one is left behind. A world where CF finally stands for Cure Found.

Every donation, every share, every bit of support, brings us closer to this goal and means the world, not just to Lotties family, but to the families who live this every day. Thank you, from the bottom of my heart 💛