Myositis Support and Understanding Association (MSU) is a patient-centered, all-volunteer 501(c)(3) nonprofit organization founded by myositis patients, for myositis patients and caregivers.
MSU is instrumental in helping to improve the day-to-day lives of patients impacted by the group of rare, complicated, autoimmune muscle, skin, and multi-organ diseases, the idiopathic inflammatory myopathies, generally referred to as myositis.
In this effort, we place a large focus on patient and caregiver support, offering live online video support and education sessions and various educational and compassionate support groups. We offer more than support, including education, patient financial assistance, access to research and clinical trials, advocacy, and more. Register for your free MSU membership and join us to make a difference in the myositis community.
Visit Understandingmyositis.org to learn more.