Jason Moore
My Story
On 23rd April I will be running the London Marathon for the Cystic Fibrosis Trust, a cause very close to my heart.
My Son Luca was diagnosed with CF at 3 weeks old, we later found out he has incredibly rare genes and he is only 1 of 4 in the world with his genotype. Unfortunately, this means Luca is in the 10% who is unable to access the wonder drug that has been currently changing the lives of many CFers.
By completing the marathon, i hope to raise awareness and vital funds for the CF trust’s research into treatments and cures.
Thank you for your support 💛