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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

Webinar

Getting Ready for Winter

Dr Elizabeth Price, BSSA Trustee took part in a Webinar for SRUK about preparing for winter. The webinar has lots of top tips and advice.

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News

Dr Elizabeth Price - Updating Sjögren's Guidelines Podcast

Oxford University Press Podcast with Dr Elizabeth Price.

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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.

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RAIRDA Survey

RAIRDA - Survey Report

Thank you to everyone who took part in the RAIRDA survey. A report has now been published regarding the results.

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Clinical Trials

Taking Part in Clinical Trials

Have you ever thought about taking part in a clinical trial? If so, take a look at our article on the risks and the benefits.

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Latest Forum Posts

Scar Healing?

Hi everyone.  I was diagnosed with Sjoegren's many years ago now. I had a... more

Lumbar Puncture

Hello Everyone Has anyone had it suggested that they have a lumbar puncture... more

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