top of page
The Leanne Fund was founded in 2009 by the Mitchell family as a lasting legacy to their daughter, Leanne, who died of Cystic Fibrosis aged 21.
Leanne was an incredibly special young woman, adored by her family and all who knew her. Leanne had an incredible strength and determination to live life to the full, making the most of every precious moment. Leanne's life was inspirational and the Fund represents Leanne's heartfelt desire to bring happiness to other people's lives.
Through the unique services of The Leanne Fund, children and young people affected by CF are able to access the support they need, whenever it is needed.
bottom of page