The last time I did fundraising for Cystic Fibrosis, I was throwing myself out of a small aeroplane for a tandem skydive.  This time, it's another huge challenge - running a marathon.  

Many of you will know that I'm fairly new to this running lark.  Indeed those of you who've known me a while will know me as 'Tracy Walker' for good reason!

After being motivated by my success at running the Oxford Half Marathon last year & subsequently disappointed at not getting a place in the London Marathon, Ian & I decided to look elsewhere & entered the Geneva Marathon on 12th May 2019.

The training plan is underway but I'm currently overwhelmed by what lies ahead and convincing my mind is more of a struggle than convincing my legs.

However, it's a challenge and that's what I've signed up for.  I'm running in memory of my sister, Emma, who sadly lost her life to Cystic Fibrosis in 1998 aged just 22.  We are now at a stage of finding out whether CF will affect the next generation of our family, also knowing that life changing drugs are available for those living with CF but sadly not available to be prescribed due to wrangles with cost between the NHS & drug companies.  

Please help me by donating a few pounds & also signing the petition below (you may need to copy/paste)

https://petition.parliament.uk/petitions/231602?fbclid=IwAR32gJrHO-7RO5COdHIbcq3QrJKkkQ_VddmigsW2SOcSXEYG-imAa74WFvE

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.