Muscular dystrophy 


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Media last reviewed: 20/08/2013

Next review due: 20/08/2015

Support groups

Muscular dystrophy can affect you emotionally as well as physically. Support groups and organisations may help you understand and come to terms with your condition better. They can also provide useful advice and support for those who care for people with MD.

There are several national charities that offer support for people affected by MD, such as the Muscular Dystrophy Campaign. You can also ask your GP or other healthcare professionals treating you about local support groups.

There are also some national support groups that promote research or provide support for specific types of MD, such as Action Duchenne and the Myotonic Dystrophy Support Group.

The muscular dystrophies (MD) are a group of inherited genetic conditions that gradually cause the muscles to weaken. This leads to an increasing level of disability.

MD is a progressive condition, which means that it gets worse over time. It often begins by affecting a particular group of muscles before affecting the muscles more widely.

Some types of MD eventually affect the heart or the muscles used for breathing, at which point the condition becomes life threatening.

There is no cure for MD, but treatment can help manage many of the symptoms.

Why it happens

MD is caused by changes (mutations) in the genes responsible for the structure and functioning of a person's muscles.

These mutations cause changes in the muscle fibres that interfere with the muscles' ability to function. Over time, this causes increasing disability.

The mutations are often inherited from a person's parents. If there is a known family history of MD, your GP may be able to refer you for genetic testing and counselling to evaluate the risk that you might develop the condition or have a child with MD, and to discuss the options available to you.

Read more about the causes of MD and genetic testing for MD.

Types of muscular dystrophy

There are many different types of MD, each with somewhat different symptoms. Not all types of MD cause severe disability and many do not affect life expectancy.

Some of the more common types of MD include:

  • Duchenne muscular dystrophy – one of the most common and severe forms, it usually affects boys in early childhood; men with the condition will usually only live into their 20s or 30s
  • myotonic dystrophy – a type of MD that can develop at any age; life expectancy is not always affected, but people with a severe form of it may have shortened lives
  • facioscapulohumeral muscular dystrophy – a type of MD that can develop in childhood or adulthood, it progresses slowly and is not usually life threatening
  • Becker muscular dystrophy – closely related to Duchenne MD, but it develops later in childhood and is less severe; life expectancy is not usually affected so much
  • limb-girdle muscular dystrophy – a group of conditions that usually develop in late childhood or early adulthood; some variants can progress quickly and be life threatening, whereas others only develop slowly
  • oculopharyngeal muscular dystrophy – a type of MD that usually doesn't develop until a person is 50-60 years old and doesn't tend to affect life expectancy
  • Emery-Dreifuss muscular dystrophy – a type of MD that develops in childhood or early adulthood; most people with this condition will live until at least middle age

Read more about the types of MD and diagnosing MD.

Who is affected?

More than 70,000 children and adults in the UK have MD or a related condition.

Duchenne MD is the most common type of MD and affects around one boy in every 3,500 in the UK. The second most common type is myotonic MD, which affects around one person in every 8,000. 

Facioscapulohumeral MD is believed to affect around 1 in every 20,000 people in the UK, which would make it the third most common type.

Treating muscular dystrophy

Although there is no cure for MD, a range of treatments can help with the physical disabilities and problems that may develop. These can include:

  • mobility assistance, including exercise, physiotherapy and physical aids
  • support groups to help deal with the practical and emotional impact of MD
  • surgery to correct postural deformities such as scoliosis 
  • medication such as steroids to improve muscle strength, or ACE inhibitors and beta-blockers to treat heart problems

New research is looking into ways of repairing the genetic mutations and damaged muscles associated with the condition. There are currently promising clinical trials for Duchenne MD. Search for clinical trials for muscular dystrophy.

Read more about treating MD.

Page last reviewed: 31/07/2013

Next review due: 31/07/2015


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The 3 comments posted are personal views. Any information they give has not been checked and may not be accurate.

InformationManager said on 03 June 2014

Hi, I'm the Information Manager at the Muscular Dystrophy Campaign.

The Muscular Dystrophy Campaign are here to support families affected by muscle-wasting conditions, including muscular dystrophy, providing free information, support and advice to individuals and families affected by muscle-wasting conditions.

Our advocacy service is available to all and is dedicated to fighting for access to the health services, employment, benefits or equipment to which you are entitled.

Our friendly staff in the care and support team are available from 8:30am to 6pm Monday to Friday. If they can’t help, they will always point you in the right direction of people who can.

If you need to talk, give them a ring on our freephone helpline on 0800 652 6352 or drop them a line at

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another_hobson said on 26 January 2013

And I'm more than a little disappointed to see that the comment left by "Davesdad" on 14th October 2011 has not been responded to. Without the support and practical guidance of the MD Campaign, its specialist care advisors and its Neuromuscular Centre in Winsford - and the new one in Coventry, a lot of us would be even further up the creek! I am also appalled to see that these pages are only reviewed every 2 years, given the rapidity of change in medical research and consequent ramifications for our treatment by others and management by ourselves, carers and families. There is no mention either of the "National Service Frameworks for long-term conditions" - search on this site for that because you won't find it on the main disability page. And if you can spare the energy, try to find out about the Specialised Commissioning Group in your area, if necessary via your MP. I'm not sure whether the one relating to neuromuscular services is fully functioning yet, but it should be before long. Promised have been made to us collectively, and in constrained financial circumstances it may be easy for these to get overlooked. The system may need reminding from time to time - collectively we can make a difference.

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Davesdad said on 14 October 2011

I am a ltiile disappointed that I could find no information about any local support network and would suggest you contact the Muscular Dystrophy Campaign in order to update the fact that there is an excellent support network for sufferers from MD

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