Physical branch meetings are currently cancelled due to COVID-19. However there are virtual activities being run by some branches. Please contact your local branch for more information.

We hope you find the information on these pages helpful. Our team is working tirelessly to provide up to date advice in relation to the COVID-19/Coronavirus pandemic. Record numbers of people are now turning to NASS for support, and we hope to be here for everyone. Our helpline and advice service are only possible thanks to donations from people like you.

If you are able to make a donation to NASS today, we'd be so grateful.


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
People Sally Helpline

By your side

We're here to help, with information on medication, self-management, benefits and more, from an understanding community

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Latest updates

My AS My Life

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

Updated shielding advice

Download some great pointers about how best to continue to shield whilst following the new government guidance.

Gold Standard Time to Diagnosis

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.

Our Impact in 2019

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.

Your stories

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 smile

See all supporter stories

Alex's journey to diagnosis

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

Rachel's story

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

Kathy's Story

How Woking & Weybridge branch came together to continue their hydrotherapy.

Read the full story

Stuart's story

After being diagnosed with axial spondyloarthritis, Stuart found that a change in lifestyle and work helped him manage the condition.

Watch the full story

Get involved

Make new friends. Make a difference. Supporting our campaigns could transform axial SpA (AS) futures

Get involved