My Story

This April, I will be lucky enough to participate in the 2024 TCS London Marathon, proudly running for the Cystic Fibrosis Trust.

As many of you might know, Cystic Fibrosis is very close to my heart. My youngest child, Alexander who is 6, has this hereditary, sometimes life limiting disease that affects mainly the lungs and in Alex's case, the pancreas too. The youtube video below gives you a brief description of what it is like to live with Cystic Fibrosis.

Alex is such a strong boy, tackling up to 40 tablets a day, having physio twice a day, regular hopsital visits plus many more things to battle on a daily basis. He always has a smile on his face.

I want to run for this charity so that they can continue devoloping 'Wonder Drugs' like Kaftrio & Kalydeco that Alex can now take. There is not a cure for Cystic Fibrosis, but with the more money raised through events like this, it gives the Cystic Fibrosis Trust more funds to develop more medicines and, maybe one day, a cure.

Please donate to this great cause. I will be so proud to run the marathon for my boy and the CF trust/community so any help will be appreciated. I will be doing various things throughout the coming months to raise as much money as possible, so please support me wherever you can.

Thank You!

https://www.youtube.com/watch?v=4IGz5p4n8Fg&pp=ygUXd2hhdCBpcyBjeXN0aWMgZmlicm9zaXM%3D