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.
The BSSA is changing to Sjögren's UK! This will include a brand new look and a brand new website. Please bear with us as we make final changes before it's launch.
more details here
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.
more details here
Oxford University Press Podcast with Dr Elizabeth Price.
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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
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.
more details hereHi, I'm not sure if it's just me. I haven't received anything on this forum since, is... more
My son keeps telling me to apply for this, but I don't thinks that Sjogrens qualifies,... more
Our website is moving to a new address!
This transition will start on September 9th and will be completed by Septemeber 16th.
During this period, you may experience some disruptions or find that the website is temporarily unavailable. The fourm will be closed to new posts during that time but will be reinstated on our new page once the transition is complete.
We apologize for any inconvenience this may cause.
Thank you for your patience, and we look forward to welcoming you at our new home!
In case of any questions or problems contact us at office@sjogrensuk.org.