My Story

Dear All,

In June 2019, I was diagnosed with Mast Cell Activation Syndrome (MCAS) after months of terrifying, unexplained illness. Before my diagnosis, I could barely walk. Eating and drinking became almost impossible. I was physically frail, mentally foggy, and utterly lost in a body I no longer recognised.

That’s why the fact I’ll be running the London Marathon in 2026 is nothing short of a miracle. It’s only been possible thanks to the unwavering love of my family and friends, the strength and solidarity of the mast cell disease community, compassionate and knowledgeable doctors, and—crucially—access to the right treatment.

Mast cell disease is unpredictable and often invisible. It looks different in every person, making it incredibly hard to diagnose. For many, it means living in fear of food, of fragrances, of reactions that can strike without warning. It is isolating. It is exhausting. It is life-altering.

But with the right care and support, there is hope. That’s why I’m running. To raise awareness. To help fund vital work. To make sure no one facing this condition has to walk that path alone.

Please stand with me. Your support could help change lives—just like mine.