I am taking on Walk Your AS Off to raise money to support people with axial SpA – a progressive, inflammatory and chronic condition of the spine and joints, causing extreme pain, exhaustion and limited movement.
It affects 1 in 200 people in the UK – twice as many as multiple sclerosis or Parkinson’s. If left untreated and symptoms are not managed, axial SpA can permanently fuse the spine and joints. It’s an invisible and misdiagnosed condition with no cure. It works silently, leaving people feeling isolated and powerless, and can make basic daily tasks and full-time employment very difficult, or even impossible.
NASS is the only charity in the UK dedicated to supporting people with axial SpA, and they don’t receive any government funding. Your donations make their work to support the physical, mental and financial wellbeing of people with axial SpA possible. Thank you for supporting NASS and people with axial SpA.
Adults in the UK
1 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.
Average age
Axial SpA (AS) is a condition that affects young people. Symptoms start late teens to early twenties, with the average age of onset being 24.
Years to diagnosis
The current average delay to diagnosis from when symptoms start is 8.5 years, by which irreversible damage to the spine may have occurred.
Mental Health
59% of people with axial SpA (AS) report experiencing mental health problems compared to 25% of those with musculoskeletal conditions overall.
National Axial Spondyloarthritis Society
Ground Floor, Unit 6, Cambridge Court, 210 Shepherds Bush Road,
London, W6 7NJ
Telephone: 020 8741 1515
Email: For more information contact fundraising@nass.co.uk
NASS is a registered charity in England and Wales (1183175) and Scotland (SC049746)
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