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.

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National Axial Spondyloarthritis Society

We are the National Axial Spondyloarthritis Society (NASS) and we are here to transform the diagnosis and care of people living with axial SpA. Axial SpA works silently. We don't.

All about axial SpA

Latest updates

An infographic showing cost of delayed diagnosis in axial SpA

Waiting, broke and invisible : The true cost of delayed diagnosis

£196,000 is a high price to pay to wait for a diagnosis. Yet, that’s the cost of a delayed diagnosis of axial SpA, according to initial research results launched by NASS today.

Front cover image of the book Unflip by Jen Parker

Unflip by Jen Parker : A memoir about life with axial SpA

Jen Parker shares how receiving a diagnosis at 23 flipped her world upside and and what its like to live with axial SpA while juggling parenthood and running her own business. She will be donating £1 from every sale of each paperback to support NASS and help others living with AS.

Group of doctors working together in clinic. Medical personnel in uniform.

Join our Champions in Primary Care programme

The programme is to support a group of clinical champions in primary care and community services and together help end diagnostic delay in axial SpA.

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

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
Image of Kate Liberty wearing her NASS T-shirt and holding her cat who is wearing a a NASS bandana

Kate's story

Kate's is taking on Walk Your AS Off to raise awareness about what its like to be young and living with axial SpA.

Read the full story
Recent image of Richard Warden

Richard's story

Richard talks about his journey to diagnosis in the 1960s and how he has learnt to manage the pain over the last 50 years.

Read the full story

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.

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Get involved

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

Get involved