Celebrating 15 Years of The Leanne Fund: A Legacy of Love, Support and Hope

2025 marks an incredible milestone for The Leanne Fund – 15 years since the charity was founded in memory of Leanne Mitchell. From its beginnings as a volunteer-led organisation in the Highlands and Islands, The Leanne Fund has grown to become a beacon of support for children, young people and families affected by Cystic Fibrosis (CF) across almost every corner of Scotland.

Inspired by Leanne’s own wish to bring happiness to others living with CF, the Fund has continued to grow in reach, compassion, and impact. Today, we are proud to support over 450 individuals and families, offering a unique range of services that are shaped by the needs of those we serve—from emotional and practical support, to fitness equipment, inpatient care packages, crisis grants, and one-of-a-kind special experiences.

Our 15th anniversary year is not only a time to reflect, but a time to celebrate just how far we’ve come—and to push forward with even more passion and purpose.

We launched our anniversary celebrations with a sweet and joyful event, Let’s Cele-Bake with The Hebridean Baker, bringing together families, supporters and star bakers in a fun-filled day of community and cake.

Next came the spectacular Rainbows & Roses for Cystic Fibrosis Anniversary Ball at the Cabarfeidh Hotel in Stornoway. It was a night to remember—filled with love, laughter, and heartfelt celebration.

In June, our much-loved Leanne Fund 5K/10K will bring together families, friends and runners of all ages for a lively and uplifting day of fun and fundraising, with prizegiving and lunch at Sgoil an Rubha.

And still to come, our brand-new Dusk2Dawn Challenge invites you to walk or run 15K, 30K or 45K under the stars in a celebration of endurance and community spirit.

More events and campaigns will follow throughout 2025, each one a chance to connect, reflect, and support those affected by CF.

From the early days in Stornoway to now supporting families across the country, our mission remains the same:

Bringing hope to children and young people living with Cystic Fibrosis.

Sharing the burden of families caring for loved ones with this lifelong illness.

Changing lives through small acts of kindness and compassion.

To everyone who has supported us on this journey—thank you. Your generosity, dedication, and belief in our work have made these 15 years possible.

Here’s to the next chapter. Together, we will continue to carry Leanne’s legacy forward—one rainbow, one rose, one act of kindness at a time.