Cystic Fibrosis Trust

Jason Moore

Jason Moore

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 💛

Cystic Fibrosis Trust

Raising for:

Cystic Fibrosis Trust
638%

Funded

  • Target
    £2,000
  • Raised so far
    £12.8K
  • Number of donors
    111

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 💛