What difference does your money make?
For every £1 we spend, 83p goes directly to improving the lives of people with AS. Our community thrives when we’re backed by people like you.
For every £1 we spend, 83p goes directly to improving the lives of people with AS. Our community thrives when we’re backed by people like you.
From the more visible physical changes to the less obvious invisible symptoms that many suffer, NASS is fighting on all fronts to try to raise awareness. There is currently no cure for axial SpA (AS).
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.
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.
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 report suffering mental health problems compared to 25% of those with musculoskeletal conditions overall.