Today, 24 April, NASS has launched its first Peer to Peer Network at the British Society of Rheumatology Conference. The network is open to any healthcare professional working in axial SpA, whether in the NHS or private practice
By joining the Peer to Peer Network, healthcare professionals will be joining our mission to transform axial SpA care and diagnosis. The network is part of the Act on Axial SpA programme, which aims to drive down the 8.5 year delay to diagnosis of axial spondyloarthritis by introducing the world’s first Gold Standard diagnosis time of just one year.
It’s an informal but structured group, providing the opportunity to link with others, share good practice and discuss ideas.
There are two ways to be involved:
- webinars in May and October
- and by signing up to a quarterly newsletters in Spring, Summer, Autumn and Winter.
Visit https://www.actonaxialspa.com/peer-to-peer-network-and-hcp-toolkit/ to sign up and join our community
Notes for editors
1 About the National Axial Spondyloarthritis Society (NASS)
At NASS we transform the diagnosis and care of people living with axial SpA. Axial SpA works silently. We don’t.
2 About Act on Axial SpA.
The Act on Axial SpA campaign aims to drive down the 8.5 year delay to diagnosis of axial spondyloarthritis by introducing the world’s first Gold Standard diagnosis time of just one year.
The campaign is led by NASS in partnership with Norfolk & Norwich NHS Foundation Trust and RUH Bath NHS Foundation Trust and funded by UCB (www.ucbpharma.co.uk).
Go to www.actonaxialspa.com to find out more.