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Juvenile Myasthenia Gravis (JMG)
What is it?
Juvenile Myasthenia Gravis (JMG) is a lifelong condition that usually begins before age 18. It is the most common of the types of MG in children and young people (the other being Transient Neonatal MG), and most commonly affects white teenaged girls.
In JMG, antibodies generated by the immune system – which normally fight off viruses – mistakenly attack muscle nerve receptors, leading to muscle weakness. Medications and treatments are available to help your child tackle their symptoms.
The outlook for younger patients with Juvenile MG is good. With proper treatment and care, your child can lead a full life.
Diagnosis for MG
If you think your child is experiencing symptoms of Juvenile Myasthenia Gravis, here’s how to get a diagnosis for them
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Treatment of MG
What can you do to alleviate the condition, and what treatments are available?
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Living with a child with Juvenile MG
Living with a child with Juvenile MG can mean coping with uncertainty. Learn how to control your child’s symptoms day to day
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