The symptoms of Sjögren's syndrome include:
See a GP if you have symptoms of Sjögren's syndrome that do not go away or are bothering you.
If needed, they can refer you to a specialist for further tests, such as:
- blood tests
- an eye examination
- a lip biopsy – where a tiny piece of tissue from inside your lip is removed and examined under a microscope
Find out more about the tests for Sjögren's syndrome.
There's currently no cure for Sjögren's syndrome, but there are several treatments that can help, such as:
- eye drops that keep your eyes wet (artificial tears)
- sprays, lozenges (medicated sweets) and gels that keep your mouth wet (saliva substitutes)
- medicine that helps your body produce more tears and saliva
If you have Sjögren's syndrome, there are some things you can do to help relieve your symptoms.
Sjögren's syndrome is caused by the immune system (the body's defence against infection), damaging healthy parts of the body. This is known as an autoimmune condition.
The condition usually affects areas of the body that produce fluids, such as tears and saliva. But other parts of the body, such as nerves and joints, can also be affected.
It's not clear why the immune system stops working properly.
It may be linked to:
- genetics – some people may be born with genes that make them more likely to get an autoimmune condition
- hormones – the female hormone oestrogen may play a part, as the condition is much more common in women than men
Primary Sjögren's syndrome is where you do not have any other related conditions.
Sjögren's syndrome is a long-term condition that does not usually get better on its own, although the symptoms can often be treated.
For some people it may just be a bit of a nuisance, while for others it can have a big impact on their daily life.
Some people may develop complications of Sjögren's syndrome, such as problems with their vision or lungs.
There's also a slightly increased risk of a type of cancer called non-Hodgkin lymphoma.
If you're diagnosed with Sjögren's syndrome, ask your doctor about what you can expect.
You may also find it useful to contact organisations such as the British Sjögren's Syndrome Association (BSSA) for advice and support.