Tough Mudders
Get a team together to take on a Tough Mudder course!
Sign me upLooking for a challenge event with a twist to raise money to support people affected by axial SpA? Look no further than these amazing obstacle courses!
Get a team together to take on a Tough Mudder course!
Sign me upPerfect for your friends and family to have a lot of fun together whilst raising money to support people with axial SpA.
Sign me upIf you are a corporate team interested in fundraising for NASS, please email fundraising@nass.co.uk or call 020 8741 1515 and 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.