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
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
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 smileSee all supporter stories
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
Make new friends. Make a difference. Supporting our campaigns could transform axial SpA (AS) futuresGet involved