My AS, My Life is a resource hub from NASS to help you build the confidence and skills you need for those times when you have to manage your axial SpA (AS) condition on your own.
It includes self-management guides, videos, blogs and links to a whole range of issues covering both your physical and mental health.
Each event will be hosted live on the NASS Facebook page, then uploaded to the My AS, My Life webpage.
Here are dates … Read this article
Talia Dean meets Dasha and Gillian to learn more about axial SpA (AS)
Singer-songwriter, Talia Dean, made a big announcement in January 2021. In 2020 she was diagnosed with axial SpA (AS). Watch this video as she meets Dasha and Gillian, who live with the disease, and starts her journey towards becoming an #ASWarrior. #TaliasASJourney
See Talia’s story in the BBC article, 15 January 2021:
‘My back pain was misdiagnosed for 15 years – now I can’t dance… Read this article
NASS are delighted to launch the second in their series of three videos explaining what Ankylosing Spondylitis is and how it affects people.
The animation ‘Ankylosing Spondylitis – Not just Back Pain’ describes how AS can affect other joints, tendons and ligaments, along with other areas including the eyes, bowels and skin.
We hope you find the video interesting.
Please do share it to raise awareness of how AS affects 200,000 people in the UK.
The current delay to diagnosis of ankylosing spondylitis (AS) stands at 8.5 years. NASS are committed to reducing this delay to diagnose. There are many factors impacting on this delay but an important issue is the recognition of AS in primary care and prompt referral on to rheumatology.
NASS have worked in partnership with the British Society for SpondyloArthritis (BRITSpA) to sponsor an eLearning course on ankylosing spondyloarthritis (axial spondyloarthritis) (AS) on the Royal College of General Practitioners (RCGP) website. … Read this article