It has been 2 years since my Dad has passed away from MND after living with it for a year. I’ve seen the devastating effect that Motor Neurone Disease has on the individual and families like mine, slowly taking away their movement, speech, and independence, while leaving the mind fully aware. Far too many families suffer in silence.

Next April 2026. I will be cycling 900 miles in 14 days to every Premier League and Women’s Super League football stadiums to raise money for Motor Neurone Disease and for our shared love of the game. I’m a complete novice when it comes to cycling, but this challenge is my way of testing my resilience, honouring my dad, and using what I have to help other families facing this devastating illness.

Receiving a diagnosis of motor neurone disease is unbelievably hard news. There is no cure. There is no effective treatment. Average life expectancy is 1-3 years from onset of symptoms.

The MND Association are doing incredible work, funding research, supporting families, and raising awareness for people living with this disease. Their work makes a real difference for families like mine. But people with MND don’t have the time to wait.

Thank you so much for any support or donations,

Rachel