Cyclists Gear Up for Tees Valley Ride Supporting MND Association

RUCK ROOTS
Thursday, 02 April 2026 at 10:58
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What began as a tribute has become a movement—seven years on, Roland Walls’ legacy continues to drive change and raise vital funds for people living with motor neurone disease.
Article submitted by the MND Association.
Seven years after he died from motor neurone disease, Roland Walls will be remembered at a special fundraising event being held this summer.

Roland, whose friend Peter Rees is a keen supporter of Darlington Mowden Park RFC, is the inspiration behind Roland’s Rides – a cycling event being held in and around the Tees Valley on 7 June.

Cyclists can choose from three distances – a novice and family ride of 25km, a social ride of 50km and an elite ride of 100km - with all the rides starting and finishing at Darlington Mowden Park RFC Stadium on Neasham Road, with the kind support of the club.
Being held for the seventh year, Roland’s Rides has already raised more than £25,000 to support people living with MND in the region and fund ground-breaking research.
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For more information about the challenge and how to get involved, visit the Roland's Ride page.
The MND Association is very proud to partner with RUCK to help raise awareness of motor neurone disease (MND).
MND is a disease which damages the nerves which send messages to the muscles. It moves fast, leaving people unable to speak, move or even breathe.
Six people are diagnosed with MND every day in the UK.
There’s no cure. Yet.
In February, the Association launched its new research and innovation strategy – a roadmap which will take us closer to discovering tomorrow’s treatments.
Working alongside people with MND, their families and experts in research, the Association has built a strategy around four objectives to help us understand, detect, discover and innovate.
Within five years, the Association will spend at least £20million each year on world-class research which gives us the greatest hope for the future. That money will allow the Association to:
  • Answer the big questions about how and why people develop MND to target potential treatments;
  • Fund the creation of tests so MND can be detected at a much earlier stage and understand how it will develop in each person to ensure they get the best care possible;
  • Lead the charge towards tomorrow’s treatments for people with all forms of MND;
  • Fund innovations in healthcare to improve the support available to people with MND right now.
Every donation made to the Association really matters.
To find out more about our work, visit our website.
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