Cystic fibrosis (CF) is a life-limiting genetic condition affecting more than 10,000 people across the UK. It affects the lungs and digestive system and can cause chronic infections and reduced lung function. Currently, half of those with CF will not live past age 41.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.

David's daughter was diagnosed with cystic fibrosis at birth, and while she has grown into a happy, bubbly, energetic four-year-old, there are aspects of her life that she has to deal with and confront daily in order to try to mitigate the effects of this life-limiting condition. She has probably had more visits to hospital than many healthy people would hope to have in their lifetime, undergoes physiotherapy sessions twice a day, digests a heavy concoction of tablets and antibiotics daily, and isn't allowed to do certain activities that others wouldn't think twice about.

Spurred on by a fantastic fund raising ride from London to Paris in 2016, and encouraged by the shared enthusiasm of two new recruits (Chris and Tim), we have this year decided to take on the mountains and ride from Milan to Monaco, through the Alps, over three days in late September. For some of us who are more used to a leisurely cycle ride in to work, or the occasional circuit round Richmond Park, this will be a bit of a game changer!

Dave, Alan, Chris, Ed, James/Fred, Henry, Tim, and Will