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British Sjögren's Syndrome Association - BSSA

The British Sjögren's Syndrome Association (BSSA) 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 more than 1800 members, the BSSA is dedicated to providing mutual support and information to individuals affected by this disabling disease.

Latest News from BSSA


Live Webinar - Chronic Fatigue, Monday 14 June 2021 5PM BST

Sjogren Europe and the BSSA invite you to a live webinar about chronic fatigue. Presented by Professor Wan Fai Ng.

more details here

RAIRDA launches survey for patients living in Wales

RAIRDA has launched a new survey for people living in Wales with rare autoimmune rheumatic diseases (RAIRDs).

more details here

The Impact Sjögren's Sydrome Has on Sexual Functioning and Intimate Relationships

Do you want to take part in a research study being conducted at Northumbria University, to help understand the impact Sjögren’s Syndrome has on sexual functioning and intimate relationships?

more details here

Dr Elizabeth Price - Updating Sjögren's Guidelines Podcast

Oxford University Press Podcast with Dr Elizabeth Price.

more details here
Looking after yourself

BSSA Webinar - Looking After Yourself

The BSSA was delighted to hold its very first live webinar. It was presented by Dr Elizabeth Price, Consultant Rheumatologist at the Great Western Hospital in Swindon. Dr Price is also BSSA Medical President and Trustee.

more details here

Latest Forum Posts

New member - Is this typical?

Hi all. I am a new member, male 55 y.o., and joined the BSSA after many GP... more

Is there some hope at last ?

Maybe in a few years' time. Google :  Israeli scientists move closer to... more

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