Myasthenia Gravis: Symptoms, Crisis Signs and Rehabilitation
Myasthenia Gravis, commonly shortened to MG, is a chronic autoimmune neuromuscular condition that causes fluctuating weakness in voluntary muscles. Weakness often becomes more noticeable with activity and may improve after rest.
What Is Myasthenia Gravis?
MG affects communication between nerves and muscles at the neuromuscular junction. In autoimmune MG, antibodies interfere with proteins needed for nerve signals to activate skeletal muscles effectively.
The weakness is not simply ordinary tiredness. It may vary during the day, worsen after repeated use and affect different muscle groups from one person to another.
Common Symptoms
Eyes
Drooping of one or both eyelids, blurred vision or double vision.
Face and speech
Changes in facial expression, soft or nasal speech and difficulty speaking for long periods.
Chewing and swallowing
Chewing fatigue, choking, coughing during meals or difficulty swallowing food, drinks and tablets.
Neck and limbs
Difficulty holding the head up, raising the arms, climbing stairs, walking or maintaining balance.
Why Symptoms Can Fluctuate
Symptoms may be milder after rest and worse after repeated activity. Infection, heat, emotional stress, surgery and certain medicines may also worsen weakness in some people.
Do not stop, start or change medication based on an article. People with MG should check new medicines, supplements and over-the-counter products with their neurologist, doctor or pharmacist because some may aggravate symptoms.

How Is MG Diagnosed?
A neurologist may use the clinical history, physical examination, antibody tests, electrical studies and imaging of the thymus. Other conditions can cause similar symptoms, so weakness should not be self-diagnosed.
Treatment depends on the MG subtype, symptoms and medical status. It may include medication, therapies that alter the immune response and, for selected people, thymus surgery. These decisions belong to the neurology team.
Myasthenic Crisis Is a Medical Emergency
Breathing weakness may not always look dramatic at first. Do not wait for the person to become exhausted or blue before seeking help.
What Is the Role of Physiotherapy?
When MG is medically stable, physiotherapy may help maintain mobility, strength, balance and participation in daily activities. The programme must reflect fluctuating weakness and avoid excessive fatigue.
- Assess mobility, transfers, walking and falls risk.
- Plan short activity periods with adequate rest.
- Use low-to-moderate exercise only when clinically appropriate.
- Monitor form and stop before weakness causes unsafe compensation.
- Provide strategies for safe movement and energy conservation.
- Coordinate with neurology, respiratory, speech therapy and occupational therapy when required.

Pacing Daily Activities
Pacing means planning tasks before fatigue becomes severe. It is not complete inactivity. The person may break tasks into smaller stages, alternate demanding and lighter activities and schedule rest before weakness interferes with safety.
Where possible, important activities may be planned for the time of day when strength is usually better and in relation to the medical plan set by the treating team.
Exercise Principles for Stable MG
- Begin below the level that triggers marked weakness.
- Use short sets and longer recovery periods.
- Avoid exercising to failure or trying to push through deteriorating form.
- Keep the environment cool if heat worsens symptoms.
- Choose seated or supported options when balance is limited.
- Stop if speech, swallowing, vision, neck control, gait or breathing worsens.
- Review prolonged post-exercise deterioration with the medical team.

Eating, Swallowing and Communication
Difficulty chewing or swallowing requires medical review and may need assessment by a speech and language therapist and dietitian. Physiotherapists should not provide swallowing treatment outside their scope.
Practical planning may include eating when strength is better, allowing adequate time and following texture or posture advice provided by the swallowing team. Choking or inability to manage saliva requires urgent attention.
Multidisciplinary Care
MG management may involve neurology, nursing, respiratory care, physiotherapy, occupational therapy, speech and language therapy, dietetics and primary care. The exact team depends on the person’s symptoms and goals.

When to Contact the Medical Team
- Weakness is becoming more frequent or severe.
- New double vision, eyelid drooping or neck weakness appears.
- Walking, transfers or daily tasks become less safe.
- Chewing, speaking or swallowing becomes more difficult.
- Symptoms change after starting a medicine or during infection.
- Recovery after ordinary activity is taking progressively longer.
Frequently Asked Questions
Is Myasthenia Gravis contagious or directly inherited?
Myasthenia Gravis is not contagious. Most autoimmune MG is not directly inherited, although genetic factors may influence susceptibility. Congenital myasthenic syndromes are different genetic conditions.
Does weakness improve with rest?
A hallmark of MG is weakness that can worsen with activity and improve after rest. However, symptom patterns vary, and sudden or severe deterioration requires medical assessment.
Can people with Myasthenia Gravis exercise?
Some medically stable people may benefit from individually prescribed, low-to-moderate activity with adequate rest. Exercise should not be taken to exhaustion, and the plan must consider respiratory, swallowing, balance and medication-related factors.
What is a myasthenic crisis?
It is severe weakness affecting breathing, and sometimes swallowing, that requires emergency medical care. Difficulty breathing, inability to speak full sentences, weak cough or rapidly worsening swallowing must not be managed as ordinary fatigue.
Can physiotherapy replace neurological treatment?
No. Neurology leads diagnosis and medical treatment. Physiotherapy may support mobility, strength, balance, pacing and functional goals when the person is medically stable and care is coordinated.
Why Choose Physiomobile?
Physiotherapy should match the individual’s condition, function and goals. Physiomobile provides flexible options to support assessment and ongoing rehabilitation.
Centre or home visits
Choose centre-based or home physiotherapy, subject to clinical suitability, coverage and appointment availability.
Individualised planning
Assessment guides the treatment focus, exercises and progression. Outcomes vary between individuals.
Practical ongoing support
Receive clear education, home-exercise guidance and progress reviews based on your response and function.
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Need rehabilitation support after medical assessment?
Physiomobile can review whether physiotherapy at a centre or at home is appropriate. We may request medical information or clearance, particularly when breathing, swallowing or rapidly changing weakness is involved.
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Medical note: This page is for general education and does not replace neurological diagnosis, medication advice or emergency care.
