Story

On 1st March, I’ll be lining up for my first (and probably last 😉) half marathon — a long-held dream finally coming true.

I’ll be running in memory of my dad, a keen runner, who we lost after his fourth battle with cancer.

But most of all, I’ll be running for a cause very close to my heart ❤️: Lynch Syndrome UK.

Our family has been deeply affected by cancer, much of it linked to this inherited genetic condition. In simple terms, it means being born with a higher risk of developing certain cancers at a much younger age — for our family as early as 28. I was diagnosed myself at 43.

If we are here today, it is thanks to early detection, regular screening and close medical follow-up.

👉 Lynch Syndrome UK works to:

• Promote screening and prevention

• Support families facing a diagnosis that is still too little known

• Share information and the latest research

If you’re able to support us, donations (even a few pounds) can be made here.

Every contribution makes a real difference to families affected by Lynch syndrome.

🙏 Thank you so much for your kindness, support and encouragement.

On 1st March, I won’t be running alone — family members and a close friend will also be taking part in the half marathon or the 10K, with others cheering us on from the sidelines ❤️

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Updates

Thnak you to all. I have run the race and made it across the finishing line with my frinefds and family's support. May the funds raised be a boost to Lynch Syndrome UK ans help in a little way towards the amazing work they do.

Updated on Wed, March 4 2026, 4:39 PM

Supporting

Lynch Syndrome UK

LSUK was founded in early 2014 by a group of people that met on a social media support group originally set up by the late Janet Norridge. Being frustrated by the lack of information and stories of erratic screening regimes throughout the UK, we came together to change things for people with LS and their families for the better.

We achieved registered charity status, after much hard work, in May 2015. As a charity, we aim to offer support and the latest information to all people with LS. 

We are passionate in our mission to raises awareness both to the medical profession and the general public about this little known genetic condition and in the process helping to save lives.

£565.00 raised of £500.00 target by 22 supporters

£565.00 donated

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