Kate and Jake Jordan are organising a series of events across the year along with their family and friends, to raise money for the Cystic Fibrosis Trust as their baby girl Maya was diagnosed with Cystic Fibrosis (CF) at 2 weeks old. The fund raising events will lead up to Jake completing a sky dive in 2026.

CF is one of the UK's most common life-threatening genetic conditions that affects the internal organs, especially the lungs and the digestive system causing a wide range of challenging symptoms affecting the entire body. 

Kate and Jake are determined to raise as much as possible to help raise awareness and support The Cystic Fibrosis Trust in their research and to find a cure.

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.

Best wishes

Kate, Jake and Maya 🌻

Edit - 02/04/2025

We wanted to say a huge thank you to everyone who has donated so far. We are overwhelmed with the support we have received already and we managed to hit our initial target within 3 days!

As we have events coming up we have increased the target, ‘we won’t stop until CF does’ 💛