How do I know if I have ankylosing spondylitis?
You will need to confirm a diagnosis of AS through your doctor or a rheumatologist (a medical specialist in bone, joint and muscle problems). AS only affects a very small proportion of the population, about 0.5 per cent. Both men and women are affected, with the condition being more common among males. There is a familial predisposition to AS, meaning that the risk of developing AS is increased if a relative is affected. A gene called HLA B27 is associated with AS and can be detected in a blood test. You can ask your doctor about this test. Your doctor may suggest x-rays or scans which can also help with making a diagnosis.
The most commonly affected region when you have AS is the sacroiliac joints, where the spine joins onto the pelvis. Sometimes, if the only symptom is recurrent back pain, the diagnosis is missed, especially because AS can start when you are younger (usually in your 20s, but can also start in younger and older people). Often the symptoms come and go, or you have ‘flare ups’.
If you are experiencing stiffness and pain in your spine and other joints and/or tendon pain that is impacting your ability to do your daily activities (work, exercise, sleep), then it is important to see your health professional.
Here are some of the common symptoms:
I’ve had pain for three months, if it’s not ankylosing spondylitis what could it be?
Other inflammatory joint and muscle conditions can have similar features to AS. It is very important to seek an opinion from your doctor or health professional to get an appropriate diagnosis—especially if your pain is ongoing or keeps flaring up. Your doctor may suggest a laboratory test to confirm the diagnosis. A rheumatologist is often the best person to make this diagnosis and to check if you have any other different health conditions.
How effective is physiotherapy for treating ankylosing spondylitis?
Physiotherapy forms one component of an overall management plan for AS. The best science or evidence guidelines for the management of AS recommends physiotherapy as a component of care with a focus on education, activity, and exercises including stretching, strengthening exercise, and aerobic exercise (that is, exercise that gets your heart going).
Physiotherapists can also help you learn how to pace activity and exercises, to manage pain flare ups and use exercise to help manage physical and mental wellbeing. Physiotherapists can also help you to manage other conditions commonly associated with AS, including more brittle bones (osteoporosis, osteoarthritis, shoulder pain, and tendinopathies (like Achilles pain and tennis elbow). Ask your physiotherapist for help.
What can I do at home?
You can do a lot to manage your AS. Getting a good health team around you makes a big difference. You need to take control of your AS—your health team is there to coach you, guide and support your management. Your doctor or rheumatologist will advise you about specific medicines that are appropriate for AS. These are very important to take as they control disease activity and can limit joint and soft tissue damage, help to control pain and allow you to keep moving.
Learning about AS, the triggers for your ‘flare ups’, the role that mood and stress can play, the value of good quality sleep, regular exercise, and good nutrition are all really important. Speak to your health professionals about how to develop a management plan that works for you.
Your management plan should include the following:
How long until I have some relief from my pain?
Everyone is different! AS can vary from mild to severe, so getting relief will depend on your specific case and general health. Ask your doctor or health professional to guide you about when you can expect relief. Also ask about what medicines might be helpful and what you can do yourself at home.
Your physiotherapist will be able to give you helpful exercises and guidance about how to manage your pain and stiffness.