There's currently no cure for muscular dystrophy (MD), but a variety of treatments can help to manage the condition.
As different types of MD can cause quite specific problems, the treatment you receive will be tailored to your needs. As your symptoms develop, the healthcare professionals treating you will advise on the options.
New research is investigating possible future treatments. Improved genetic testing can help if you're concerned about passing MDon to your children.
As MD progresses, it weakens your muscles and you gradually begin to lose mobility and strength. These physical problems can be helped with the following:
Once the chest muscles become too weak to control breathing properly, you may need machines to assist with your breathing and coughing, particularly while sleeping.
In people with Duchenne MD, corticosteroid medication (steroids) has been shown to improve muscle strength and function for six months to two years, and slow down the process of muscle weakening.
Steroid medication for Duchenne MD is available in tablet orliquid form, and current research suggests a daily dose is most effective. However, long-term use of steroids is associated with significant side effects such as weight gain and excessive hair growth.
Recent research has also shown thata creatine supplementcan improve muscle strength in some people with MD, while causing few side effects.
Creatine is a substance normally found in the body that helps supply energy to muscle and nerve cells. It's often available as a supplement from pharmacies and health food stores.
If you have MD anddecide to take creatine supplements, make sure you mention this to your doctors (GP and specialist).
People with some types of MD find swallowing increasingly difficult as the condition progresses. This is known as dysphagia and it can increase your risk of choking or developing a chest infection , if food and liquid get into the lungs.
Depending on the severity of your swallowing problems, there are a number of treatments that can be used. For example, a dietitian may help you alter the consistency of your food and you may be taught some exercises by a speech and language therapist, to improve your swallowing.
If necessary, surgery can also be used to treat swallowing problems. Thismay involve a minor procedure to cut one of the muscles in your throat, ora small balloonmay be inflated in your gullet (oesophagus) to expand it.
If MD progresses to a point where you're unable to get enough nutrition by swallowing, a feeding tube (gastrostomy or PEG) may need to be surgically implanted into your stomach through your abdomen (tummy).
Some types of MD can affect the heart muscles and the muscles used for breathing. When the condition has progressed to this stage, it can become life-threatening.
It's important that your heart function is assessed regularly once MD has been diagnosed. For Duchenne and Becker MD, an electrocardiogram (ECG) examination of heart rhythm will be carried out at regular intervals, and you may also have an echocardiogram from time to time. A magnetic resonance imaging (MRI) scan may also be used to check for heart problems.
If any damage to your heart is detected, you may be referred to a cardiologist (heart specialist) for further tests and possibly more frequent monitoring.
You may be prescribed medication to treat your heart problems, such as ACE inhibitors to relax your arteries and make it easier for your heart to pump blood around your body, or beta-blockers to control irregular heartbeats (arrhythmias or dysrhythmias).
In some cases of myotonic or Emery-Dreifuss MD, a pacemaker may be fitted to correct an irregular heartbeat. A pacemaker is a small, battery operated device that can be implanted into your chest to regulate your heartbeat.
In some severe cases of MD, surgery may be necessary to correct physical problems that can occur as a result of the condition.
For example, if your child has Duchenne MD, there's a chance they'll develop scoliosis . Surgery can correct the scoliosisor prevent it getting worse, although there haven't been any trials to evaluate its effectiveness.
Other kinds of surgery may be used to treat specific symptoms:
If you or your child may benefit from having surgery, you'll be referred to a specialist to discuss the procedure and the risks involved.
New ideas for MD treatments are currently being developed.
Speak to your GP or specialist if you're interested in taking part in a clinical trial (a form of research that tests one treatment against another). You can also browse the database of clinical trials for MD .
Your GP or the healthcare professional treating you may know of any recent developments in healthcare that may benefit you.
Some examples of current research ideas are explained below.
Trials are now in progress in theUK and Netherlands to see if "exon skipping" may be a useful way of treating Duchenne MD. Exons are sections of DNA that contain information for proteins.
In Duchenne and Becker MD, some of the exons are missing or duplicated, which can interfere with the dystrophin protein being produced.
Researchers are currently investigating ways of "skipping" additional exons in the dystrophin gene. This could mean that more dystrophin would be produced, reducing the severity of MD symptoms.
Current trials are focused on treatment that would apply to Duchenne MD, but it may become applicable to Becker MD in the future.
Stem cells are cells that are at an early stage of development. This means they have the ability to turn into any type of cell in the body.
Some research is currently focusing on whether stem cells can be turned into muscle cells and used to regenerate damaged muscle tissue.
The muscular dystrophies (MD) are a group of inherited genetic conditions that gradually cause the muscles to weaken, leading to an increasing level of disability.
There are many different types of muscular dystrophy (MD). All types cause muscle weakness, but the areas affected and the severity of the symptoms are different.
In most cases, muscular dystrophy (MD) runs in families. It usually develops after inheriting a faulty gene from one or both parents.
The age at which MD is diagnosed will vary, depending on when the symptoms first start to appear.
As different types of muscular dystrophy can cause quite specific problems, the treatment you receive will be tailored to your needs.
Genetic testing may be useful for prospective parents who have a family history of muscular dystrophy (MD) and are worried about passing the condition on to their children.