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 BSSA 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.
LATEST NEWS
GETTING READY
FOR WINTER
Dr Elizabeth Price, BSSA Trustee took part in a Webinar...
read moreDR ELIZABETH PRICE UPDATING SJÖGREN’S GUIDELINES PODCAST
Oxford University Press Podcast with Dr Elizabeth Price.
read moreBSSA Webinar
Looking After Yourself
The BSSA was delighted to hold its very first live...
read moreLATEST FORUM POSTS
Benefits for joining the BSSA:
- Providing information and support to those affected by the condition
- Distribute a variety of literature including an informative quarterly magazine
- Operating a national members' helpline facility
- Hosting regular regional meetings throughout the UK
- Link members through our ‘make a friend’ scheme
- Annual medical meeting with talks from consultants and experts in Sjögren's Syndrome
- Online members forum
- Full access to our informative website
£25.00
£30.00