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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.
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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
Find out more about axial SpA and discover resources to help you take control of your AS.
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Join NASS and become part of a community who are having a real impact and influence on the work we do.
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Find out how you can help power our services so people like Steve don’t have to face the financial pressure of axial SpA alone
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Our symptom checker will take you through a few questions that will help you understand whether you should speak to your GP about axial SpA.
£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.
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.
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
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
Kate's is taking on Walk Your AS Off to raise awareness about what its like to be young and living with axial SpA.
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Richard talks about his journey to diagnosis in the 1960s and how he has learnt to manage the pain over the last 50 years.
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Alex's journey to diagnosis was long and painful but he finally found a diagnosis when his osteopath suggested a referral to rheumatology.
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Rachel made the change from teaching RE to Karate and talks about how it has helped her live with Axial Spondyloarthritis.
Read the full storyMake new friends. Make a difference. Supporting our campaigns could transform axial SpA (AS) futures
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Raising awareness has the power to change the future. Show you care by shouting about our research or sharing our stories.
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From cake baking to skydiving, our supporters’ generosity raises vital funds for our important work. What do you want to do?
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Real life stories are invaluable to NASS. We’d like to hear from supporters who are willing to be a case study.
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