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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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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No one should face financial insecurity because they live with axial SpA. Your donation can make a life-changing difference to people like Robin.
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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.
We are delighted to welcome everyone back on Saturday 24 September for a day of information sharing, talks and fun workshops.
Stretch-tember is our new virtual stretch challenge. It is easy to take part you just need to commit to stretch throughout September while fundraising for NASS.
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
Dasha shares how healthcare professionals struggled to make a link between her symptoms and axial SpA, leaving her feeling “lost and scared”.
Read the full 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
Jen Parker shares her journey to diagnosis at 23 and how she is raising awareness of the challenges of living with axial SpA while juggling parenthood through her memoir, Unflip.
Read the full story
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 storyMake new friends. Make a difference. Supporting our campaigns could transform axial SpA (AS) futures
Get involved
Raising awareness has the power to change the future. Show you care by shouting about our research or sharing our stories.
More about campaigning
From cake baking to skydiving, our supporters’ generosity raises vital funds for our important work. What do you want to do?
More about fundraising
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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