Story

Dan's story

Daniele is a supporter who has run the London Marathon several times for Heart Research UK.

My heart and I have been through a lot together. As a teenager, it kept up with me on the football pitch. As an adult, it powered ultramarathons, Ironman races, and countless predawn training sessions. But our relationship changed when I was 14. That’s when I first felt it – a sudden, jarring flutter in my chest, like a gear slipping mid-stride. Back then, doctors brushed it off. So I did too.

For years, I dismissed it. The episodes came and went, brief, unsettling interruptions during games or long runs. I learned to pause, breathe, and wait for my pulse to settle. But two years ago, the flutters grew longer and more intense. My heart would rocket to 220 beats per minute during easy jogs, leaving me dizzy and worried. Finally, after a lifetime of athleticism and denial, I got answers: supraventricular tachycardia (SVT), a glitch in my heart’s wiring that had gone undiagnosed for 20 years.

In December, I had a cardiac ablation, a procedure to fix the misfiring circuits. This wasn’t a defeat, it was a necessary pit stop.

Recovery has been humbling. My first post-op walk around the block felt miles away from trail ultras and triathlons. But progress is progress. I’m relearning my limits, swapping 100-mile weeks for deliberate, steady miles.

To the team who diagnosed me after decades of uncertainty, thank you. To researchers improving treatments for conditions like SVT, keep going.

Donate to take on heart disease

Your kind donations will save lives

Donate today

Share your story

Sharing your journey of living with or knowing someone who has had a heart condition is invaluable. Your experience inspires, helps and supports people across the UK.

Tell your story
Chris's story

Chris

Chris is a dedicated member of the Patient and Public Network. Driven by his personal experience of heart diseases, he hopes to help create a future where lesser lives are lost to heart diseases.

Read more
Gilbert's story

Gilbert

Gilbert is a dedicated member of the Patient and Public Network at Heart Research UK, helping build the future of innovation and patient care.

Read more
Peter's story

Peter

Peter is an active member of the Patient and Public Network, using his own experiences to help inspire the research that will support people in the years ahead.

Read more
Jaye's story

Jaye

Jaye is a member of the Patient and Public Network, using her lived experience to help shape the heart research of tomorrow.

Read more
All Stories