Drs. Kaveh Ardalan, Andrea Knight, and Alison Manning discuss juvenile myositis’ impact on mental health and how parents can address them.
Building friendships with others in the JM community can be difficult. Since JM is a rare disease, medical common ground might be a state away.
This video provides an overview of juvenile myositis for families newly diagnosed with juvenile dermatomyositis (JDM) or juvenile polymyositis (JPM).
Practical tips on how to navigate your child’s school system. Presented by Michelle Best (special education and mental health advocate) and Sue Carpenter (special education resource specialist teacher).
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