Ava was diagnosed with Cystic Fibrosis at three weeks old which was life changing news for us all. Cystic Fibrosis is a genetic life-limiting condition that affects around 11,000 people in the UK - that’s 1 baby in every 2,500 births. CF affects multiple organs in her body due to horrible thick sticky mucus buildups. However, due to medical advances, Ava is absolutely thriving and is the happiest, healthiest little girl with the biggest smile a lots of giggles.

Ava’s nearest and dearest have decided to take part in the Kiltwalk where we will walk 14 miles from Clydebank to Balloch. We are hoping to raise money for a very special charity - The Leanne Fund. The Leanne Fund is a Scottish CF Support Charity based in Stornaway on the Isle of Lewis (her big brothers name 🥹) and Harris.

“The Leanne Fund is the foremost Cystic Fibrosis support organisation in Scotland - bringing hope to those affected by the illness, sharing the burdens that CF brings, and significantly changing the lives of sufferers and their families through a range of social, practical, emotional, and financial support services.”

The Leanne Fund have been there to support Ava during more challenging times, as well as during her hospital admission. They really take care of our little CF Superstars when times are tough. They are a very special and unique charity and we are so grateful for them and for their support. So help us support them by donating even the smallest amount 🥰.

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