In January 2015, I was diagnosed with Multiple Sclerosis.

Before that, I’d already experienced some alarming symptoms — losing vision in my right eye temporarily, losing sensation around my abdomen and half of my face, and even losing sensation from the waist down for a period of time. Countless MRI scans, lumbar punctures, and blood tests finally confirmed the diagnosis.

After being diagnosed, I started a new treatment. The treatment itself came with harsh side effects, and at times it felt like things were getting worse before they got better. Not long after starting the treatment, I lost sensation in my right arm from the elbow down and had no ability to control my right hand. Needless to say, I changed my treatment shortly after to something else. Over time, my arm improved to just numb fingertips.

Ten years on, my legs remain in constant pain — some days are manageable, others are much tougher — but with treatment, painkillers, and determination, I’ve kept going.

Sport has always been my outlet. Before moving to Canada in 2018, I found community in CrossFit, and I picked it back up after moving back to the UK in 2020. In 2019, I was proud to represent Canada Rugby League 🇨🇦🏉 — proof that MS wasn’t going to stop me chasing challenges.

But in August 2024, I suffered a serious back injury. I had to quit the gym, my motivation disappeared, and even walking felt like a challenge. On 18th September 2025, I’ll undergo spinal decompression surgery with a discectomy to try and get back on my feet properly.

And that’s where the next chapter begins.

In April 2026, I’ll be running the London Marathon 🏃‍♂️ — for the MS Society.

Yes… the guy who hates running, lives with MS, and is about to have spinal surgery has decided to take on 26.2 miles. Bonkers, right? But what’s life without a challenge?

My goal is to raise £2,500 to help fund research, treatment, and support for people living with MS. Every donation, no matter the size, makes a difference.