Share your experiences of support for managing axial SpA while living in Norfolk

We’re working on an exciting new project in Norfolk.

We’re looking to create support and resources for people living with axial SpA in Norfolk and the surrounding area, so we need your help. Share your views on what’s needed in your area to support you in being active with your axial SpA.

If you have axial SpA and live in Norfolk, you can get involved in a number of different ways. Hopefully there’s a way that works for you. If you have any questions, please email zoe@nass.co.uk

Join an online group discussion:

Share your ideas for information and support we can provide locally. We have two dates available:

Thursday 19 February, 11:00-12:00 – more information and book
Tuesday 24 February, 18:00-19:00 – more information and book

Spaces are limited, so please book your place as soon as possible.

Complete our short anonymous survey:

It takes less than 10 minutes to share your views and experiences in our survey. All responses are anonymous and will help us create resources and support.

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 project is supported by funding from the Peter Harrison Foundation.

The project is led by NASS Programme Manager, Zoë Clark, who lives with axial SpA, and Sally Dickinson, NASS Head of Information and Support Services.