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EPDA - European Parkinsons Disease Association EPDA - European Parkinsons Disease Association EPDA - European Parkinsons Disease Association EPDA - European Parkinsons Disease Association EPDA - European Parkinsons Disease Association EPDA - European Parkinsons Disease Association EPDA - European Parkinsons Disease Association
EPDA - European Parkinsons Disease Association
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Frequently asked question (FAQ)

I look in the mirror and find it difficult to recognise myself, as my face seems so lacking in expression. Is there anything I can do to improve this?

Facial expression is a good example of an important kind of communication that is not speech. We all, perhaps without realising, take a lot of notice of the facial expressions around us and it is often the first thing we notice about people. We may decide to give the boss a wide berth because he looks grumpy, or pass several people in the street before we see someone who looks friendly enough to ask for directions.

There are several things you can do to help yourself and the first is to try to maintain a good posture. If you can, try to look someone ‘in the eye’. This will help with posture. Perhaps surprisingly, our second suggestion entails looking in the mirror. Facial exercises, for example, frowning and screwing up your eyes, then moving down your face to grins, yawns and smiles, can help to keep the muscles of your face more mobile and are best done in front of a mirror. Try saying a suitable word or phrase while doing these exercises – you could say ‘lovely to see you’ when you smile, for example, or ‘I’m bored to tears’ when you yawn. So practise frowning, then opening and closing your eyes, wrinkling your nose, puffing out and sucking in your cheeks, whistling, smiling and yawning. A local speech and language therapist will be able to suggest other, individualised, exercises for you to try.

The third thing you can do is to tell your relations and friends that lack of facial expression is one of the symptoms of Parkinson’s and that they should be aware that your face may be giving out inaccurate messages. We are afraid that you may have to repeat this information many times because our normal response to facial expression is deeply ingrained and we can be disconcerted and upset by, for example, the absence of smiles, even when we have been told that it is a common symptom of Parkinson’s. Partners, relatives and friends may need to be helped to understand and make allowances for this feature, especially in the early days after diagnosis.



This FAQ has been taken with permission from "Parkinson's: Answers at Your Fingertips" by Bridget McCall (Published by Class Publishing)
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