My lovely little nephew, Max, was born with Haemophilia in 2023; a rare genetic blood disorder. Although he is the happiest, chunkiest, cutest baby (whats bias?) I've ever seen, he requires lifelong treatment for his bleeding disorder. The advancements made in these treatments are thanks to a range of amazing organisations including The Haemophilia Society, and Max has benefited from this and has already had an operation that will change his life.

I am honoured to say I will be running 26.2 miles/42.2km on behalf of The Haemophilia Society in the 2025 London Marathon! 🏃🏽‍♀️🩸 Any donations to the cause are welcomed and I can't thank you all enough for all of the support I have received already.

The Haemophilia Society (THS) is the only UK-wide charity for everyone affected by a genetic bleeding disorder. They are free to join and have more than 5,000 members.

One in 2,000 people in the UK have a diagnosed bleeding disorder, including conditions such as haemophilia and von Willebrand disorder, that result when the blood cannot clot properly. As many as a third of bleeding disorder diagnoses have no known family history, which means a diagnosis can come completely out of the blue.

THS campaign for what matters to their members, lobbying government, the NHS and clinicians to demand excellent care and safe, effective treatment, which is available to all.

🩸How to Support for Free🩸

🩸Give Blood! If you are able to donate blood then you will literally be saving a life.

🩸Join the Team: If you were lucky enough to get a place in the public ballot for a marathon or any event then sign up to join the team and raise money for a great cause.

🩸Explore The Haemophilia Society website to see the great work they do, find resources and join their campaigns. https://haemophilia.org.uk