These can include:
- dry mouth
- difficulty swallowing
- difficulty in controlling dentures
- difficulty cleaning your teeth
- increase in tooth decay
Dry mouth (xerostoma)
Saliva is really important for good mouth health:
- It helps you taste your food.
- It lubricates food to help you swallow.
- It is antibacterial and has enzymes to help you eat and digest food.
Without enough saliva you may experience a dry mouth. A dry mouth can lead to higher rates of tooth decay and gum disease. It can increase your risk of getting tooth decay in the exposed roots. It may also cause dentures to become loose and hard to control.
A dry mouth can also increase the damaging effects of sugar on your teeth. Because of this it is important to watch what you eat and when you eat.
Some Parkinson’s drugs can reduce the flow of saliva to your mouth. Tell your dentist if you experience this as they can discuss options which might help. They may ask you what drugs you take, so take a list of your medication to your appointments.
Tell your GP, specialist or Parkinson’s nurse too as they may be able to prescribe different treatments that may not cause this problem. Saliva substitutes are also available. You can ask your dentist or local pharmacist about them.
The following tips may help reduce dry mouth.
- try to take frequent sips of water
- chew sugar-free gum
- use lip salve to protect your lips if needed
- remove dentures at night to give your mouth a chance to recover
- eat a healthy, balanced diet
- smoke – it makes the dryness worse
- use mouthwashes that your dentist or doctor have not prescribed – they may contain alcohol, which can increase dryness
- suck sugary sweets to increase saliva – this will increase decay and other mouth problems
- sip sugary drinks between meals – this will also increase decay and other mouth problems
Some people with Parkinson’s complain of a burning mouth feeling. This can be due to a dry mouth or taking levodopa. If you experience this, speak to your dentist or health professional.
If you have Parkinson’s you might experience swallowing difficulties because your jaw and face muscles have weakened. This can also affect how well you can chew.
Find out more: see our information about eating, swallowing and saliva control.
Drooling is common for people with Parkinson’s. You may experience this because you cannot swallow as well as you used to.
Drooling happens if you swallow less because saliva pools in your mouth and may overflow from the corners of your mouth.
Drooling can lead to a sore mouth and your posture might make it worse. Those who have a stooped, head-down position can find it hard to seal their lips. This can make it harder to control saliva flowing from the mouth. So it’s important to speak to your health professional for the right help and support.
You can also try these simple exercises at home in front of a mirror to try help prevent drooling. They’ll help you become more aware of what your lips are doing and how tight you need to hold them closed to keep saliva in.
- Close your lips as tightly as possible and hold for a count of 4, relax, then repeat 5 times.
- Smack your lips together.
- Stretch your lips in a wide smile, hold for a count of 4 and relax.
In addition, you can try aids to help you to remember to swallow. For example, a device with a timer that prompts you to swallow. Your Parkinson’s nurse can help you find a device that is right for you. A speech and language therapist may also be able to help.
It is important to visit the dentist regularly. This will identify and treat issues quickly and prevent them from getting worse.
Your dentist will advise you how often you need a check-up. Get any specific problems looked at between appointments.
There are cleaning techniques and equipment that can make good dental and mouth health easier if you have Parkinson's. For example, a toothbrush with a bigger handle may give you a better grip. Ask your dentist for advice on what is right for you.
If you’re unable to get to your dentist, ask if home visits may be possible. Many dentists do them or they can refer you to a colleague who does. Alternatively, they can give you information on how to get help.
Will my Parkinson’s mean I need to see a specialist dentist?
It’s important to tell your dentist that you have Parkinson’s and how it affects you.
Most dentists will be able to treat people at all stages of the condition.
If your dentist feels you need specialist care, they will refer you to a colleague on the General Dental Council’s ‘special care’ register.
If you have to have dental surgery, talk to your dentist about Parkinson’s symptoms you experience and how these may affect your operation.
You should also tell your dentist about your drug regime so that you continue to get the right dose when you have your operation.
If you’ve had deep brain stimulation and you now need to have a dental operation, you will need to take antibiotics. This will help make sure that you don’t get an infection or another issue that could affect your deep brain stimulation device.
If you wear dentures Parkinson’s may mean you have difficulty controlling them. This could be because of:
- problems controlling your facial muscles
- loss of muscle tone
- dry mouth
- pooling of saliva
- poorly designed dentures
- old and very worn dentures
- loose dentures that rub parts of your mouth and cause blisters or ulcers. (Loose dentures may also make it more difficult for you to eat and speak properly.)
Ask your dentist to check your dentures and suggest any improvements. This will help if you find your dentures difficult to control.
If you have dentures, removing them will help you clean all surfaces more easily.
We know lots of people would rather have something in their hands to read rather than look at a screen, so you can order printed copies of our information by post, phone or email.
Looking after your oral hygiene when you have Parkinson's
Parkinson’s can make it more difficult to look after your teeth and mouth health. Read our tips for maintaining good oral hygiene.
Last updated September 2018. We review all our information within 3 years. If you'd like to find out more about how we put our information together, including references and the sources of evidence we use, please contact us at [email protected]