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Cystic Fibrosis is a life threatening, debilitating disease that seriously affects the lungs and digestive system. The average life expectancy of a CF sufferer is just 31 years. There is currently no cure.
Each week, five babies in this country are born with Cystic Fibrosis and each week, three young people lose their lives to the disease.
There is a huge lack of funds for Cystic Fibrosis research, and therefore all the proceeds from our event will go to the CF Trust in the UK and the CF Foundation in the USA, both of whom are carrying out pioneering research into new treatments and cures.
Your support will help to make a vital difference.
The Liv Committee