Symptoms of motor neurone disease
The initial symptoms of motor neurone disease often affect certain areas of the body before eventually becoming more widespread.
It's important to visit your GP as soon as possible if you have the typical early symptoms of motor neurone disease. There's evidence that specialist care can improve overall survival.
The symptoms usually follow a pattern that falls into three stages:
- the initial stage
- the advanced stage
- the end stage
The initial symptoms of motor neurone disease usually develop slowly and subtly over time. It can be easy to mistake early symptoms for those of several unrelated conditions that affect the nervous system.
In about two-thirds of people with motor neurone disease, the first symptoms occur in the arm or leg. This is sometimes called limb-onset disease. These symptoms include:
- a weakened grip, which can cause difficulties picking up or holding objects
- weakness at the shoulder, making lifting the arm above the head difficult
- tripping up over a foot because of weakness at the ankle or hip
These symptoms are usually painless and may be accompanied by widespread twitching of the muscles (fasciculations) or muscle cramps, and there may be visible wasting of the muscles with significant weight loss.
In a quarter of cases, problems initially affect the muscles used for speech and swallowing. Increasingly slurred speech (dysarthria) is usually the first sign of this type of motor neurone disease, and may be misdiagnosed as a stroke.
As the condition progresses, it may become increasingly difficult to swallow (dysphagia), and be misdiagnosed as a blockage in the throat.
In extremely rare cases, motor neurone disease starts by affecting the lungs, rather than affecting them at the end of the condition. This is called respiratory-onset disease.
In some cases the initial symptoms are obvious, such as breathing difficulties and shortness of breath.
In other cases the symptoms are less noticeable, such as waking up frequently during the night because the brain is temporarily starved of oxygen when lying down. This can make the person feel very tired and unrefreshed the next morning, sometimes with a headache.
As motor neurone disease becomes more advanced, the differences between the various types of disease are less noticeable as more parts and functions of the body are affected. The rate at which the condition spreads varies, but generally remains the same for an individual (that is, it doesn't speed up, but doesn't slow down either).
The limbs become gradually weaker and the muscles in the limbs may appear progressively wasted. As a result, the person will find it increasingly difficult to move the affected limbs.
The muscles may also become stiff. This is known as spasticity. Both muscle wasting and stiffness can also cause joint aches and pains.
Speaking and swallowing difficulties
At least two-thirds of people with motor neurone disease find that speaking and swallowing become increasingly difficult as the condition progresses. However, although choking episodes can be distressing they aren't the cause of death.
Reduced swallowing can cause an excess of saliva, sometimes with drooling. Thicker saliva may sometimes be difficult to clear from the chest or throat due to weakening of the muscles that control coughing.
Some people with motor neurone disease have episodes of uncontrollable, excessive yawning, even when they're not tired. This can sometimes cause jaw pain.
Motor neurone disease can lead to changes in a person's ability to control their emotions, particularly when there's weakness in the muscles that control speech and swallowing.
One of the most common signs is when a person has episodes of sudden uncontrollable crying or, more rarely, laughter. Doctors may call this emotional lability or emotionality.
Changes to mental abilities
Occasionally, people with motor neurone disease may have significant difficulties with concentration, planning and use of language. This is known as cognitive change and overlaps with a condition called frontotemporal dementia.
The changes are usually quite subtle, making it difficult to tell them apart from the normal ageing process, and they don't normally affect a person's capacity to make their own decisions.
Up to 15% of people with motor neurone disease develop more profound frontotemporal dementia, usually soon after, or sometimes before, their first muscle-related symptoms. The affected person may not be aware that there are problems with their behaviour or personality.
As the nerves and muscles that help control the lungs become progressively more damaged, the person's breathing will become less efficient.
This may be a feeling of being very short of breath after doing everyday tasks, such as walking up the stairs. However, over time, the person may even become short of breath when they're resting.
Shortness of breath may be particularly troublesome at night. Some people find it difficult to breathe when they're lying down. Others may wake up in the night because of breathlessness.
As motor neurone disease progresses, a non-invasive breathing mask may be recommended at night to improve sleep quality and help reduce drowsiness during the day.
As motor neurone disease progresses to its final phase, a person with the condition will probably experience:
- increasing body paralysis, which means they'll need help with most daily activities
- significant shortness of breath
Eventually, non-invasive breathing assistance won't be enough to compensate for the loss of normal lung function. At this stage, most people with motor neurone disease become increasingly drowsy before falling into a deep sleep, where they usually die peacefully.
Some people with motor neurone disease have additional symptoms that aren't directly caused by the condition but are related to the stress of living with it. These may include depression, insomnia and anxiety.
Although many people with motor neuron disease may think about ending their life at some point, this isn't a common outcome, particularly with strong family and community support.
Page last reviewed: 15/01/2015
Next review due: 15/01/2017