On this page:
Key points
Ask for your breathing to be checked regularly, even if you have not noticed any changes.
There are things you can do to make breathing more comfortable, keep your energy and help keep your lungs clear.
Changing your position and the air flow around you can make breathing more comfortable.
Breathing and coughing techniques can help you expand your lungs and clear thin and runny or thick and sticky secretions (fluid made by the body, such as saliva and mucus) from your throat and chest.
Managing saliva and getting advice about eating and drinking can help keep your lungs clear.
Save your energy for the activities that matter most to you.
Your healthcare team can help you find strategies and equipment that suit you.
Get your breathing checked regularly
MND weakens the muscles you use to breathe. This can happen at any stage of MND. You might:
feel short of breath
feel more tired
notice your voice is not as loud
find it harder to breathe when lying flat
have difficulty sleeping
have headaches in the morning
have trouble coughing, sneezing, clearing your nose or throat.
You do not need to wait until you notice these changes to ask for information or support.
Regular breathing checks (assessments) from soon after diagnosis can identify changes early and help you and your healthcare team decide what support may help. A breathing assessment typically involves answering questions and performing breathing tests (“lung function tests”).
Talk to your MND clinic or healthcare team about having your breathing checked regularly.
Change your body position
The way you sit or lie can make breathing easier or harder.
Some people find breathing harder when lying flat. You may find it easier when you are:
sitting upright
supported by pillows
standing
leaning slightly forward.
These positions can help you breathe because they give your main muscle underneath your lungs (the diaphragm) more room to move.
Equipment such as an electric recliner chair, adjustable bed or wheelchair can help you find a comfortable position without using too much energy.
Ask your physiotherapist or occupational therapist about positions and equipment that may help you.
Ask about breathing exercises
Some breathing exercises may help you take deeper breaths and expand your lungs more fully.
There are exercises that address specific aspects of breathing which may help keep your breathing better for longer. Ask your physiotherapist, specialist respiratory nurse or respiratory physician which breathing exercises might be appropriate for you to try.
Keep your cough strong
Coughing helps keep saliva (spit), food and fluid out of your lungs. An effective cough also clears mucus from the back of your throat and from your lungs.
As the muscles used for breathing become weaker, your cough can also become weaker. This can make it harder to clear your lungs and may increase the chance of chest infections.
A physiotherapist can show you ways to make your cough more effective. Ask about:
breath stacking
strategies to clear saliva
whether additional equipment may help you.
You should not wait until your cough becomes weak to ask for advice.
Manage saliva
MND can make saliva harder to manage. Saliva may be thin and watery, or thick and sticky, and can change over time and during the day. For example, as the weather or room temperature changes.
Changes to swallowing, breathing, positioning, eating and medicines can all affect how easily you can clear saliva.
A speech pathologist, physiotherapist, pharmacist or doctor can help. They may suggest changes to your position, mouth care, medicines, or equipment to make saliva easier to manage.
Use air flow to make breathing more comfortable
Moving air across your face can help reduce the feeling of being short of breath (breathlessness).
You could try:
opening a window
using a handheld or room fan
keeping the room at a comfortable temperature.
If dry air is uncomfortable, ask your healthcare team whether a humidifier may help.
Save your energy for what matters
Everyday activities can take more effort as MND progresses. There is no advantage in pushing yourself until you are very tired.
Save your energy for the activities that are important to you.
You might:
pace yourself and rest before you become too tired
break activities into smaller steps
find easier ways to do everyday tasks
use technology or equipment to help you
use mobility equipment, like a wheelchair when going out
plan rest periods or naps during the day
ask other people for help.
A physiotherapist or occupational therapist can help you find ways to save your energy and recommend equipment.
Consider non-invasive ventilation (NIV) to support your breathing
Non-invasive ventilation (NIV) is a treatment that can support your weakened breathing muscles. It can help you to:
sleep better
feel less breathless
save your energy
feel better during the day
live longer.
Talk with your healthcare team about whether NIV is right for you. Use our resources to learn about NIV and to help prepare for your appointment.
Try to relax if you have difficulty breathing
Feeling like you can’t breathe can cause anxiety or worry. This can change the way you breathe and make you feel worse.
Controlled breathing and relaxation techniques may help you feel calmer and make breathing more comfortable. Sometimes medications can be used.
A calm and confident approach from a family member or carer can also help.
Ask your physiotherapist, palliative care team, specialist respiratory nurse or respiratory physician to show you techniques that are suitable for you.
Make eating and drinking easier and safer
If your swallowing or cough become weaker, food or drink may sometimes go down the wrong pipe into your lungs instead of your stomach. A weak cough can make it harder to clear.
A speech pathologist can assess your swallowing and recommend foods and drinks that are easier and safer for you to manage.
A dietitian can help you get enough food and drink and help reduce the effort when eating. If you are finding meals hard or tiring you may consider a feeding tube.
A physiotherapist can also show you and your carer how an assisted cough may help clear food, drink or saliva that goes towards your lungs instead of your stomach.
Eat enough and keep your bowels moving
Getting enough food and fluid helps maintain your energy, weight and helps your muscles work, including the muscles you use for breathing and coughing.
Tell your healthcare team if eating is becoming tiring, takes a long time or you are losing weight.
It is also important to manage constipation (difficulty emptying your bowels). Straining to empty your bowels takes effort and uses your diaphragm, the main breathing muscle. A bloated stomach can also make it harder to breathe.
Enough fluid and appropriate nutrition (food) can help. Talk to your dietitian, pharmacist or GP if constipation is a problem.
Protect yourself from chest infections
Coughs, colds and chest infections can make breathing more difficult.
Where possible, avoid close contact with people who are sick and keep up to date with recommended vaccinations.
Ask your GP or respiratory physician which vaccinations are recommended for you.
Talk about changes early
Tell your healthcare team if you notice changes in your:
sleep
energy
ability to lie flat
cough
ability to clear saliva
eating or drinking
weight
breathing.
Getting advice early gives you more time to understand your options and decide what works best for you.
Talk to your GP, neurologist, MND clinic or your healthcare team.
Questions to ask your healthcare team
You should not wait until breathing becomes difficult. Talk to your healthcare team about a breathing assessment and how they will monitor your breathing.
Use the following tools to prepare for your healthcare appointment:
NIV question builder (for creating your own question list)
Breathing and ventilation treatment with MND
Breathing and MND: about breathing assessments
Physiotherapists: a vital part of your care team
Acknowledgements
Dr Nicole Sheers, Dr Marnie Graco and Kylie Russo, from the Breathing, Exercise and Sleep Therapies (BEST) Laboratory at the Institute for Breathing and Sleep and The University of Melbourne, for clinical review and guidance.
Sources
Van Damme, P., Al-Chalabi, A., Andersen, P.M. et al. (2024), ‘European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERN EURO-NMD)’, European Journal of Neurology, 31(6), e16264. DOI: 10.1111/ene.16264.
https://pmc.ncbi.nlm.nih.gov/articles/PMC11235832
National Institute for Health and Care Excellence (NICE) 2016, ‘Motor neurone disease: assessment and management’, retrieved from https://www.nice.org.uk/guidance/NG42/chapter/Recommendations#managing-symptoms.
Silva et al. (2025), Efficacy of respiratory muscle training in improving pulmonary function and survival in patients with amyotrophic lateral sclerosis: a systematic review and meta-analysis. https://pmc.ncbi.nlm.nih.gov/articles/PMC12149620
Swan et al. 2019, ‘Airflow relieves chronic breathlessness in people with advanced disease: An exploratory systematic review and meta-analyses’, Palliative Medicine, 33(6),618–633.
Berlowitz et al. 2016, 'Identifying who will benefit from non-invasive ventilation in amyotrophic lateral sclerosis/motor neurone disease in a clinical cohort', J Neurol Neurosurg Psychiatry, 87(3),280-86.