Physio For Juvenile Myasthenia Gravis

Q: Children with JMG may experience:

Drooping eyelids or double vision.Muscle fatigue.Difficulty chewing, swallowing or speaking.Challenges with lifting, walking, or physical activity.Poor head control or postural difficulties.Fluctuating weakness affecting daily participation.

Paediatric physiotherapy for children with Juvenile Myasthenia Gravis.

Expert guidance for Kids with Myasthenia Gravis.

Helping children stay active and safe through tailored physiotherapy

Juvenile Myasthenia Gravis (JMG) can be unpredictable, often bringing fatigue and weakness that change from day to day. At PaedsPhysio, we take a sensitive, pragmatic approach to physiotherapy, supporting each child to move, play and participate safely. With an understanding of the condition’s complexity, we focus on quality of life, energy management, and gentle strengthening that fits around your child’s needs.

WHAT IS JUVENILE MYASTHENIA GRAVIS (JMG)?

What is Juvenile Myasthenia Gravis?

A pragmatic approach to managing JMG

Juvenile Myasthenia Gravis is a rare autoimmune neuromuscular condition that affects the way muscles receive signals from nerves, leading to muscle weakness and fatigability. It often begins in adolescence and is more common in girls, though younger children can also be affected. JMG can present as ocular (affecting the eyes) or generalised, involving weakness in the face, limbs, throat or even breathing muscles.

At PaedsPhysio, we know the importance of pacing and adaptability in working with JMG. Our experienced paediatric team works closely with families to create a therapy plan that supports your child’s physical development whilst respecting their limits. From early signs like droopy eyelids and fatigue, to wider mobility or postural challenges, we’re here to help children manage their condition confidently and safely.

Children with JMG may experience: expand to list like ‘Children’s Physiotherapy following Brain Injury’ section in Acquired Brain Injury Physiotherapy – Paeds Physio

Children with JMG may experience:

Drooping eyelids or double vision.
Muscle fatigue.
Difficulty chewing, swallowing or speaking.
Challenges with lifting, walking, or physical activity.
Poor head control or postural difficulties.
Fluctuating weakness affecting daily participation.

How Physio Helps Children With Juvenile Myasthenia Gravis

Because juvenile myasthenia gravis causes variable muscle weakness, physiotherapy must be carefully adjusted to avoid overexertion

At PaedsPhysio, we build individualised programmes that support strength, function and participation, with energy conservation at the heart of everything we do. Our physiotherapists prioritise quality of movement and use short, low-resistance sessions with regular rest to support ongoing activity and prevent deconditioning.

Our physiotherapy for children with JMG may include: <expand to list like ‘Children’s Physiotherapy following Brain Injury’ section in Acquired Brain Injury Physiotherapy – Paeds Physio>

Our physiotherapy for children with JMG may include:

Low-load, short-duration functional activities (e.g. sit-to-stand, stair climbing).
Postural control exercises to support head, trunk and spinal alignment.
Balance and coordination work to support gait and stability.
Respiratory physiotherapy including bubble play and breathing exercises.
Energy conservation strategies (planning, pacing, positioning, prioritising).
Stretching to prevent contractures and maintain flexibility.
Advice to support safe activity at home and school.

HONEST, PRACTICAL SUPPORT.

Honest, Practical Support.

Support for you and your child through every challenge

At PaedsPhysio, we support families through the ups and downs of Juvenile Myasthenia Gravis. Whether your child is newly diagnosed or needs ongoing physiotherapy support, our team is ready to help with expert physiotherapy, practical advice, and a friendly, understanding approach.