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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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About axial SpA (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 about our new programme to reduce the delay to diagnosis for people living with axial SpA (AS)
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Find out howNASS branches
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Updated COVID-19 / Coronavirus advice
View the latest advice from NASS for people living with axial SpA (AS)
Gold Standard Time to Diagnosis
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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.
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Our Network for younger people with axial SpA (AS)
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Chat with others and share your story
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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
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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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Kathy's Story
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Stuart's story
After being diagnosed with axial spondyloarthritis, Stuart found that a change in lifestyle and work helped him manage the condition.
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Make new friends. Make a difference. Supporting our campaigns could transform axial SpA (AS) futures
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Campaigning
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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