Our office relocation is underway, which means there may be a short delay in sending out post for up to 7 working days from Thursday 4th December. Responses to voice messages and social media comments may also take a little longer than usual during this time. We appreciate your patience and understanding during this time. Please note that orders may be delayed, and we ask for your continued patience as we work to resolve the issue.

Our helpline will continue to operate as normal, and if there are any changes, we’ll let you know straight away.

We’re really excited about this move, it will allow us to support our members on an even greater level. Thank you for your patience and understanding while we settle into our new space

The British Sjögren's Syndrome Association (BSSA)

(now with the working name of Sjögren’s UK) was founded in 1986, as a registered charity, to raise awareness of the disease and support research into its cause and treatment. A self-help organisation with around 2300 members, the Sjögren’s UK is dedicated to providing mutual support and information to individuals affected by this disabling disease.

We have regional support groups throughout the UK whose members include sufferers and supporters who work together in helping one another cope with the day-to-day challenges of this debilitating and distressing condition. Sjögren’s UK also has a helpline, we distribute a variety of literature including an informative quarterly newsletter and we award an annual research grant. There is currently no cure for Sjögren’s and the cause is still unknown.