This sheet has been written for people affected by Sjögren’s syndrome. It provides general information to help you understand how Sjögren’s syndrome affects you and what you can do to manage it. It also tells you where to find further information and advice.

What is Sjögren’s syndrome?

Sjögren’s syndrome is an autoimmune condition. The normal role of your body’s immune system is to fight off infections and diseases to keep you healthy. In an autoimmune disease like Sjögren’s syndrome, your immune system starts attacking your own healthy tissues. This results in abnormal dryness of the mouth, eyes and/or other tissues. Around half the people who have Sjogren’s syndrome also have some form of arthritis (conditions affecting the joints, such as lupus and rheumatoid arthritis). This is known as secondary Sjögren’s syndrome. Primary Sjögren’s syndrome occurs in people who do not have one of these forms of arthritis.

What are the symptoms?

Sjögren’s syndrome can affect many different parts of the body. The glands that produce tears and saliva are most often affected. Common symptoms include:

  • dry eyes (including irritation, gritty feeling or painful burning in the eyes)
  • dry mouth (or difficulty eating dry foods)
  • swelling of the glands around the face and neck.

Some people may also experience dryness in other areas of the body (such as the nose, throat, and vagina) and skin.

What causes it?

It is not known what causes Sjögren’s syndrome. It is believed to be the result of genetic factors and/or possible viral infections, which activate the immune system. This is yet to be proven in research.

How is it diagnosed?

Your doctor or specialist will diagnose Sjögren’s syndrome from your symptoms, physical examination and a range of tests. Dry eyes and mouth require further testing as they can also be caused by many other conditions or medicines. The main test to help diagnose Sjögren’s Syndrome is called a Shirmer’s test. This test involves using a strip of blotting paper to measure whether the eye produces enough tears to keep it moist. Blood tests and a biopsy of the lip (a small piece of tissue from the inside of the lower lip is removed and examined under a microscope) can also help to diagnose Sjögren’s syndrome.

What will happen to me?

Usually the outlook for people with Sjögren’s syndrome is very positive. Most people with the condition are able to live normal lives without any serious complications. There can be an increased risk for infections in and around the eyes and for problems with the teeth. This is a result of the long-term reduction in tears and saliva. In rare cases, organs such as the liver and kidneys may be involved, which can increase the severity of the condition. In a small number of people, Sjögren’s syndrome may be associated with lymphoma, a cancer of the lymph glands.

sjogren's syndrome specialist

Is there a cure?

Currently there is no cure for Sjögren’s syndrome. While there are ways you can control the symptoms, you should be wary of any products or treatments that claim to cure the condition.

What can I do?

1. See your doctor for treatment and advice. Your doctor will help coordinate your treatment. As Sjögren’s syndrome is a life-long disease, it is important to see your doctor regularly to make sure it stays under control. Your doctor may also send you to a Rheumatologist, an arthritis specialist, for further tests and treatment. Regular dental care from a dentist is also important in order to prevent cavities and dental problems. People with dry eyes should see an ophthalmologist (eye doctor) regularly to check for damage to the eye. See your doctor promptly if you notice excessive redness and pain in the
eyes as this could be a sign of infection.

2. Learn about Sjögren’s syndrome and play an active role in your treatment. Not all information you read or hear about is trustworthy so always talk to your doctor or healthcare team about treatments you are thinking about trying. Reliable sources of further information are also listed in the section below. Self management courses aim to help you develop skills to be actively involved in your healthcare.

3. Learn ways to manage symptoms. Most of the treatment for Sjögren’s syndrome is aimed at relieving symptoms of dry eyes and mouth and preventing and treating long-term complications such as infection and dental disease. Treatments may include:

  • regular use of artificial tears and lubricating ointments for the eyes to manage dryness
  • drinking water and/or using artificial saliva, mouth rinses or lozenges to relieve mouth dryness
  • moisturisers for the skin
  • avoidance of drying conditions, eg drafts from heaters and air conditioners, and exposure to dusty or windy weather, and
  • medicines prescribed by your doctor (for example, non-steroidal anti-inflammatory drugs (NSAIDs), corticosteroids or medicines that work on the immune system).

4. Live a healthy life. Stay physically active, eat a healthy diet, stop smoking and reduce stress to help your overall health and wellbeing.

5. Acknowledge your feelings and seek support. As there is no cure for Sjögren’s syndrome, it is natural to feel scared, frustrated, sad and sometimes angry. Be aware of these feelings and get help if they start affecting your daily life.

© Copyright Arthritis Australia 2007. Reviewed May 2015.
Disclaimer: This sheet is published by Arthritis Australia for information purposes only and should not be used in place of professional advice.

Source: A full list of the references used to compile this sheet is available from your local Arthritis Office. The Australian General Practice Network, Australian Physiotherapy Association, Australian Practice Nurses Association, Pharmaceutical Society of Australia and Royal Australian College of General Practitioners contributed to the development of this information sheet. The Australian Government has provided funding to support this project.

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