Скачать с ютуб Bethany's story of the wait for an axial SpA diagnosis. (Act on axial SpA) в хорошем качестве

Bethany's story of the wait for an axial SpA diagnosis. (Act on axial SpA)

Bethany lost her teenage years waiting for a diagnosis of axial SpA. Meet her as she talks to comedian Jess Fostekew about her experience (and their love of the Spice Girls). #ActOnAxialSpA. Whether or not you've got persistent back pain, find out more about the signs and symptoms at www.axialspa.com 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 Campaign funded by UCB