My Story

In November 2023 I was diagnosed with Relapsing Remitting Multiple Sclerosis, a progressive condition with no cure.

There are approximately 150,000 people in the UK living with this diagnosis.

In people with MS, the immune system attacks the spinal cord and brain, and this then affects the nerves in the body, causing mobility issues, fatigue, tingling, burning sensations and a multitude of others. 

My world was turned upside down as I was a healthy 48 year old keeping active through running, and a job as a Firefighter. 

Over 3 weeks I gradually lost feeling from the waist down, along with horrendous fatigue and brain fog. As a result I was admitted to hospital and after 8 days I was discharged with a diagnosis which would change my life forever.

I was fortunate that I regained feeling enabling me to walk again, but was left with constant fatigue, burning in my legs and feet.

One of my first questions to my MS team was 'Can I run again?'

They said you know your body so take it easy. I started by running a mile, a month after coming out of hospital and have been running since. I fought to get back to work full time too.

During my recovery I discovered the Sussex MS Centre and now regularly visit for oxygen therapy and to see others. They offer practical and emotional support to hundreds of people every year and run various classes/sessions at the Centre on a daily basis from financial advice, to physical activities, or just simply a cup of tea and a listening ear. They have helped me immensely and rely on donations and fundraising to stay open.

Since diagnosis I've been trying to challenge myself, to prove that life isn't over with an MS diagnosis. It's definitely harder and I'm sure it will get even harder.

So when I managed to get a public ballot place in the London Marathon I immediately felt I needed to payback and take on the next personal challenge. 

Thanks for your support.