Join us for a free online session to meet other people with axial SpA, get support, and learn ways to manage your condition and the impact it has on your life.
We’ll be covering:
- What axial SpA is and how it can impact you
- How axial SpA is managed
- Practical ways to manage pain and fatigue
- Creating a flare toolkit
- Keeping active
This is a practical session with short presentations and plenty of time for attendees to chat with each other. We’ll also be on hand to answer any questions you may have. Please note, we can’t answer specific clinical questions, but we can let you know which healthcare professional to contact for advice.
When are the sessions?
We currently have two different date on offer, but both sessions are the same, so please only book onto one:
- Thurs 3 April, 18.00-19.30. Find out more and book your place.
- Thurs 4 Sept, 18.00-19.30. Find out more and book your place.
The sessions run 18.00-19.30, but we’ll stay on after the call for 30 minutes to answer any other questions.
If you can’t attend either of these dates, email zoe@nass.co.uk so we can let you know about other sessions in 2025.
If you have any questions or accessibility requirements, please email zoe@nass.co.uk
Look forward to seeing you there!
Who are we?
The National Axial Spondyloarthritis Society (NASS) is the only charity in the UK dedicated to supporting people with axial spondyloarthritis (axial SpA), including ankylosing spondylitis (AS). This programme is supported by funding from the National Lottery Community Fund.
The sessions are facilitated by NASS Programme Manager, Zoë Clark, who is a healthcare professional living with axial SpA, and Sally Dickinson, NASS Head of Information and Support Services.