FAQs

This website is intended to be viewed on a desktop

What is Myasthenia Gravis?

Myasthenia Gravis (MG) is a chronic condition that can persist for years. It occurs when antibodies in the blood block the normal communication between nerves and muscles – causing muscle weakness. The condition can be unpredictable, and when not managed may leave you weak and struggling with small tasks.

  • The two most widely occurring types of MG are Ocular Myasthenia Gravis and Generalised Myasthenia Gravis (also known as gMG)
    • Ocular sees the eyelids and muscles around the eyes frequently fatigued. Most people will experience these symptoms first
    • Generalised Myasthenia Gravis (gMG) may cause you to experience weakness throughout your body – including the eyes
  • Other types of MG include Transient Neonatal and Juvenile MG

What are the symptoms of Myasthenia Gravis?

Symptoms can vary by person. Some of the most common symptoms include:

  • Muscles controlling eyelid movement are affected, causing changes in facial expressions - such as weakness around the eyes, drooping or sagging in one or both eyelids (Ptosis) – a potential cause of Ocular Myasthenia Gravis
  • Blurred vision
  • Weakness of the neck or limbs – struggling to hold your head up or having trouble walking
  • Other symptoms include shortness of breath, difficulty swallowing and dysarthria (impaired speech)

What causes Myasthenia Gravis?

Myasthenia Gravis is a condition of the immune system where it mistakenly targets a healthy part of the body, resulting in weak muscles and tiredness. Myasthenia Gravis is not considered an inherited or contagious condition. It can occur at any age but tends to develop later in life.

  • It is linked to the thymus (chest gland)
  • Sufferers of Myasthenia Gravis often have a larger than normal thymus gland

How is Myasthenia Gravis treated?

The type of treatment will depend on your age, general health, symptoms and severity of the condition. Your healthcare provider will discuss options available to you.

What can make Myasthenia Gravis worse?

If you have been diagnosed with MG, it is important to maintain a healthy, balanced lifestyle to support your wellbeing. A lack of sleep, extreme temperatures (hot showers or baths, hot food or drinks, saunas, and weather), and some chemicals like insecticides can worsen your symptoms. For more information on management and living with MG, see our help page.

Is Myasthenia Gravis life-threatening?

MG is not a progressive or terminal disorder – and though there can be life-threatening complications, such as myasthenic crisis, many people diagnosed with MG can live normal, balanced lives. There are various medications and treatment plans that your healthcare provider will discuss with you to improve your symptoms.

Is Myasthenia Gravis genetic?

Generally, MG is not inherited. If one of your family members has an autoimmune disease, it is not uncommon for other family members to also have one.

Is Myasthenia Gravis painful?

If you are suffering from MG, you will experience several symptoms associated with the condition. Generally, these symptoms include weakness of muscles (head, neck, arms, fingers and legs), but these are fatiguing and not painful.

Can I get a diagnosis for Myasthenia Gravis?

Myasthenia Gravis is a chronic autoimmune disorder where the body attacks its own neuromuscular system. As the condition fluctuates in how it affects the muscles such as the eyes, mouth and limbs, it can be difficult to get a diagnosis. See your healthcare provider for a diagnosis if you are experiencing MG symptoms so they can properly assess you. They will walk you through your symptoms and ask you about your medical history. You may need to take a series of tests to support a diagnosis.

  • Blood tests look for a high level of antibodies that may be present in people with MG
  • Genetic testing checks for conditions like MG and may be used to rule out other conditions with similar symptomology
  • Neurophysiological tests, including
    • Repetitive nerve stimulation or nerve conduction studies, which use tiny electrical impulses to see how a muscle bounces back after repeated stimulation
    • Electromyogram (EMG) tests, which measure the electrical activity of a muscle and can detect abnormal activity due to neuromuscular conditions
    • Single-fibre electromyogram (SFEMG) tests, which record the transmission from nerve to muscle
  • An imaging scan such as a CT or MRI scan checks the thymus gland – to detect if it is bigger than usual or has grown abnormally. An MRI scan is a neurological exam and will check those symptoms are not caused by issues in the brain
  • To confirm a diagnosis or to act as a guide during clinical decision making, healthcare providers may perform a short and specific assessment known as the ice test (or ice pack test) to measure whether a patient with MG can determine sensitivity
  • Healthcare providers will use Edrophonium testing when the picture is unclear. They will only recommend this test if absolutely necessary due to the risks involved

What is the Thymus Gland?

The Thymus Gland is responsible for managing our immune system. It sits inside the chest area beneath the breastbone. The gland grows during childhood and begins to get smaller after puberty. For people with MG, the gland is abnormal, and typically remains large in size.

By what other names is Myasthenia Gravis known?

Myasthenia Gravis is Latin and Greek in origin. The name comes from the meaning “grave or serious muscle weakness.” The condition is also known or referred to as “MG.”

If I have MG, are there medications to avoid?

If you are suffering from MG, your healthcare provider will need to complete a physical examination to diagnose you. Subsequently, they may prescribe medications alongside a treatment plan. It is essential to check with a healthcare professional before taking a new medicine or over-the-counter prescription as several of these can exacerbate MG symptoms. See our helpful guide on types of prescription medications to avoid or use with caution for more information.

Can I exercise with Myasthenia Gravis?

Many patients with MG find the intensity of their symptoms varies day to day. Talk to your healthcare provider about when and how to exercise. They will help you work out a plan to suit how much exercise and what type of exercise will benefit you. Be sure to exercise within your limits, take breaks and factor in short sessions, which you are more likely to tolerate better. Stopping short of muscle fatigue will prevent you from overdoing it.

Can I work with Myasthenia Gravis?

It is your decision to talk to your employer about your MG. If you decide to tell your employer about your condition, they may help provide you with support to allow you to work like any other person without MG would. A job with a stressful working environment may cause your MG to worsen. Your employer should work with you to find solutions to situations that are likely to arise – such as if you are physically unable to perform a task.

I am pregnant and have MG; what can I expect?

If you are pregnant or plan on getting pregnant, it is important to talk to your healthcare provider or a neurologist about your specific condition of MG. Together, they will help you work out the best outcomes and advise you on how MG can affect your pregnancy. Your healthcare provider should closely monitor your pregnancy.

Driving with Myasthenia Gravis

You should inform the DVLA of your condition so that they can evaluate you and check the severity of your MG. Being diagnosed with MG doesn’t prevent you from driving, but it is advisable to take necessary precautions, such as asking someone else to drive if you feel tired.

Is Myasthenia Gravis genetic?

Myasthenia Gravis is an autoimmune disease; it is not genetic. There are, however, several types of what are called Congenital Myasthenic Syndromes (CMS) – these are a group of genetic disorders whose symptoms are similar to Myasthenia Gravis. Although CMS share many symptoms with Myasthenia Gravis, the underlying causes are different – Myasthenia Gravis arises from an abnormal immune response, while CMS is due to a genetic deficiency.

What are Congenital Myasthenic Syndromes (CMS)?

Congenital Myasthenic Syndromes (CMS), sometimes incorrectly called Congenital Myasthenia Gravis, is a group of rare genetic conditions that include muscle weakness that gets worse with physical activity. Most people develop symptoms of CMS in infancy or early childhood, though they can appear all the way into adulthood. You are likely to develop CMS if you have inherited the defective gene from both parents.

There are several types of Congenital Myasthenic Syndrome:

  • Synaptic CMS is caused by a genetic error that impacts the gap between the muscle and the nerve. It can cause weakness, difficulties eating and breathing, and delayed motor milestones.
  • Presynaptic CMS is the least common type of CMS and is caused by a problem in the nerve ending. It often begins in infancy and causes weakness in the eye muscles (Ptosis), as well as difficulties talking, eating, and breathing.
  • Postsynaptic CMS is the most common type of CMS. It is caused by muscle cells with either too few acetylcholine receptors (AChRs), or AChRs which don’t stay open either too long (Slow-Channel CMS) or not long enough (Fast-Channel CMS). Symptoms range from mild to severe and include severe weakness, feeding and breathing difficulties, and delayed motor milestones.

How are Congenital Myasthenic Syndromes (CMS) diagnosed?

CMS may be diagnosed through physical examination, blood tests, Electromyography (EMG) and repetitive nerve stimulation testing (RNS), a Tensilon test, and/or genetic testing.

If you are concerned about anything you have read in this article, please seek advice from your healthcare provider.
This website is intended to be viewed on a desktop

IE-N-DA-MG-2300012. November 2023
This website has been created and funded by UCB Pharma Ltd

Images used are not of real patients.