Alex's journey to diagnosis was long and painful but he finally found a diagnosis when his osteopath suggested a referral to rheumatology.Read the full story
COVID19 / Coronavirus
NASS is closely monitoring the evolving situation in relation to COVID19 /Coronavirus. We have advice and guidance for people living with axial SpA (AS)Read more about COVID19
Helping you build the skills and confidence to take control of your AS and your life. Includes videos, blogs and downloadable guides and exercise sheets
Download some great pointers about how best to continue to shield whilst following the new government guidance.
Find out about our new programme to reduce the delay to diagnosis for people living with axial SpA (AS) from an average of eight-and-a-half years to just one year.
NASS has been changing the lives of people living with axial SpA (AS) for more than 40 years and is proud of its achievements in 2019.
Determined, brave and sometimes quirky, our inspiring supporters show us so many ways to get involved. But often, there's a painful reality behind the smileSee all supporter stories
Rachel made the change from teaching RE to Karate and talks about how it has helped her live with Axial Spondyloarthritis.Read the full story
How Woking & Weybridge branch came together to continue their hydrotherapy.Read the full story
Make new friends. Make a difference. Supporting our campaigns could transform axial SpA (AS) futuresGet involved