Join us for a free online session for people recently diagnosed with axial SpA (within the last three years). You’ll 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.
These sessions are ideal for people who have been diagnosed with axial SpA in the last three years and you’re looking for more information about the condition and how to manage it. If you have been diagnosed longer than three years, please join one of our Your SpAce meetups.
When are the sessions?
Our next session:
- Thurs 4 Sept, 18.00-20.00. Find out more and book your place.
If you can’t attend this date, email zoe@nass.co.uk so she 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.
Healthcare professionals in England
Order free postcards to invite your patients to our self-management session.