![](https://nass.co.uk/wp-content/uploads/2024/08/Steve-Barfoot-Hayling-Island-to-Paris-Bike-Ride-2-2.png)
London to Paris Cycle Ride
24th Apr 2025 ‐ 26th April 2025
Sign me upWant to challenge yourself on the bike and fundraise for NASS? Look no further than these amazing challenges!
24th Apr 2025 ‐ 26th April 2025
Sign me up15th May 2025 ‐ 17th May 2025
Sign me up25th Sep 2025 ‐ 27th September 2025
Sign me upFill in the form below to receive your welcome email and supporters’ pack to get you started on your fundraising journey. We’ll support you every step of the way.
If you have any questions about fundraising for NASS, please don't hesitate to email fundraising@nass.co.uk or call 020 8741 1515 (press option 2)
Get inspired by reading more stories of others affected by axial SpA who have chosen to fundraise to support people with axial SpA.
Read more storiesFind out why your support really does matter, the impact your support can have, and why your support has never been more urgent.
Find out more1 in 200 of the adult population in the UK have axial SpA (AS). That's twice as many as multiple sclerosis and Parkinson's disease.
Axial SpA (AS) is a condition that affects young people. Symptoms start late teens to early twenties, with the average age of onset being 26.
The current average delay to diagnosis from when symptoms start is 8.5 years, by which irreversible damage to the spine may have occurred.
59% of people with axial SpA (AS) report experiencing mental health problems compared to 25% of those with musculoskeletal conditions overall.