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Donate to our NASS Winter Appeal today to help support people like Steve: https://nass-winter-campaign.raisely.... The price people are paying for the 8.5-year delay to diagnosis is too high. Meet Steve. He waited 30 years for an axial SpA diagnosis. He had a thriving construction company but had to give it up because the pain became too much. He's one of the thousands of people hit by the £196,000 cost for an 8.5-year delay to diagnosis of axial SpA. Watch his video now to learn more about his story. 1 in 200 people live with axial SpA. Do you have unexplained back pain that could be Axial SpA? Let us know in the comments 👇or check your symptoms using our simple symptom checker: https://www.actonaxialspa.com/symptom... Enjoying this video? Subscribe! → / nasscentral 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. FOLLOW US ↓ • Facebook / nationalaxialspondyloarthritissociety • Twitter / nassexercise • Instagram / nass_exercise • LinkedIn / national-axial-spondyloarthritis-society • TikTok / nass_charity JOIN OUR COMMUNITY ↓ • Receive our monthly e-newsletter https://nass.co.uk/newsletter/ • Become a member https://nass.co.uk/get-involved/becom... • Join a Your SpAce online meetup https://bit.ly/3WbPCH4 • Find your local NASS Branch https://nass.co.uk/managing-my-as/in-... USEFUL RESOURCES ↓ • Contact the NASS Helpline for support https://nass.co.uk/contact-us/ Find out more at www.actonaxialspa.com Check your symptoms: https://www.actonaxialspa.com/symptom... #ActOnAxialSpA #ankylosingspondylitis #axialSpA #axialspondyloarthritis #axSpA #chronicbackpain Campaign funded by UCB