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Motor Neuron Disease: What you need to know?

What is Motor Neuron Disease?

The motor neuron diseases (MNDs) are a group of progressive neurological disorders that destroy cells that control essential muscle activity such as speaking, walking, breathing, and swallowing.  Normally, messages from nerve cells in the brain (called upper motor neurons) are transmitted to nerve cells in the brain stem and spinal cord (called lower motor neurons) and from them to particular muscles.  When there are disruptions in these signals, the result can be gradual muscle weakening, wasting away, and uncontrollable twitching (called fasciculation’s).  Eventually, the ability to control voluntary movement can be lost.  MNDs may be inherited or acquired, and they occur in all age groups.  MNDs occur more commonly in men than in women, and symptoms may appear after age 40.  In children, particularly in inherited or familial forms of the disease, symptoms can be present at birth or appear before the child learns to walk.

Types of Motor Neuron Disease?

The main types of MND are:

  • Amyotrophic lateral sclerosis (ALS): This is the classical MND and the most common type. About 8 in 10 people with MND have this type. Symptoms tend to start in the hands and feet. The muscles tend to become stiff as well as weak at first.
  • Progressive bulbar palsy (PBP): About 2 in 10 people with MND have this type. The muscles first affected are those used for talking, chewing and swallowing (the bulbar muscles).
  • Progressive muscular atrophy (PMA): This is an uncommon form of MND. The small muscles of the hands and feet are usually first affected but the muscles are not stiff.
  • Primary lateral sclerosis (PLS): This is a rare type of MND. It mainly causes weakness in the leg muscles. Some people with this type may also develop clumsiness in the hands or develop speech problems.

What are the symptoms of  MND?

MND is a progressive disease that usually starts slowly and gets worse over time. Symptoms sometimes starting on one side of the body and then spreading. Usually, the first things people notice are:

  • weakness in the hands and grip
  • slurred speech
  • weakness in the legs, and a tendency to trip
  • weakness of the shoulder, making lifting difficult
  • cramps and muscles twitching

Later on, people with MND:

  • have little or no movement
  • have trouble talking, breathing and swallowing

A few people with MND develop a type of dementia.

If you have MND, your sense of sight, touch, smell, hearing and taste won’t be affected.

What causes  MND?

The exact cause of MND is not known. You can’t catch MND from somebody.

Generally, MND is believed to be caused because of a combination of environmental, lifestyle and genetic factors.

Most cases of MND occur spontaneously without any identifiable cause. Around 1 in 10 cases are ‘familial’ (meaning the condition is inherited) due to a genetic mutation (or error in the gene).

If a person has an MND-related genetic mutation, their children have a 50/50 chance of inheriting the MND-related genetic mutation.

If a person in your family has MND, other people in the family can be tested to see if they have the genetic mutation.

People who inherit the genetic mutation have a high chance of developing MND, but not all people with the genetic mutation will develop MND.

How is MND diagnosed?

MND can be hard to diagnose when the symptoms first appear because it seems like a lot of other conditions at first.

You may have a range of tests, some which eliminate other conditions.

Your doctor may refer you to a neurologist who will examine you and do various tests. These may include:

What are the treatments for ALS motor neuron disease?

Although there is no cure for ALS-MND, treatments can help both to slow the disease and also to improve any symptoms you may have.

Respiratory care

In this treatment, you are given a mask ventilator system to wear overnight while you are sleeping. The machines are small and portable and you can choose from a variety of different masks to suit you. People using this have been shown not only to have longer survival but also an improvement in the quality of their lives.

Treatments to help ease symptoms

Treatments are available for many of the symptoms that you may develop with ALS-MND. These may include cramps, difficulty swallowing saliva and food, urinary symptoms and depression.

It can be fairly common for people with ALS-MND to have feeding problems. These may either be due to difficulty swallowing or to difficulty in actually feeding yourself due to the weakness in your arms and hands. Some people find that having thickened fluid and sitting very upright when eating are beneficial.

If you are losing weight as a result of having feeding difficulties then you may benefit from having a gastrostomy inserted. This is a small feeding tube that is placed through the wall of the tummy (abdomen) directly into your stomach. Your doctor will discuss this in more detail with you if this might be appropriate for you.

Most people with ALS-MND are cared for by a professional team which includes neurologists, specialist nurses, physiotherapists, speech and language therapists, occupational therapists, dieticians and counsellors. Each problem that arises is assessed and dealt with as far as possible by the relevant members of the team.

What is the outlook for motor neuron disease?

MND does shorten life expectancy, and is a fatal illness. However, there is huge variation in how quickly it progresses, and it is different in each person who has it. Muscles weakened by ALS-MND do not recover. However, weeks or months may go by where the disease does not seem to progress. Eventually, severe disability develops. As the disease becomes severe, people with ALS-MND are unable to walk, talk or eat, and need a lot of care.

How quickly does motor neuron disease progress?

Your specialist may be able to give you an idea of how quickly MND is likely to progress in your particular case. However, the outlook (prognosis) for people with ALS-MND is extremely variable:

  • About 7 in 10 people with ALS-MND die within three years of the onset of symptoms.
  • About 25 in 100 survive five years.
  • About 5-10 in 100 survive 10 years or more.

In the other, rarer types of MND, progress may be slower and the outlook better.

There are many research studies looking at different potential treatments for ALS-MND. It is hoped that new treatments will be introduced in the future.

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2022-04-22T11:49:43+00:00

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