We work to provide education, research and support to the myositis community. Find resources, learn about treatments and connect with others like you.
May is Myositis Awareness Month. Support Starts Here. Join us for awareness month activities such as webinars, fun group activities, and much more.
Myositis, an autoimmune disease, involves autoantibodies targeted against skeletal muscles. Learn more about myositis and autoantibodies.
An exploration of inclusion body myositis aimed at patients and physicians.
Cancer-associated myositis is a malignancy that develops within a year or two of a diagnosis of myositis. Learn the risk factors and treatments.
Idiopathic Inflammatory Myopathies include Dermatomyositis, Polymyositis, Inclusion Body Myositis, immune-mediated necrotizing myopathy, antisynthtase syndrome.
Myositis and Me - Dermatomyositis and More
Diagnosing Myositis, Inflammatory Myopathies, usually includes lab work, muscle or skin biopsy, EMG, MRI, and nerve conduction studies. It is not uncommon to be misdiagnosed due to the rarity of the disease.
Myositis is a rare autoimmune disease that causes inflammation in the muscles, leading to muscle weakness, pain, and fatigue.
Myositis is an incurable rare disease with no FDA-approved treatments. Off-label use of medications can help some patients, with often life-altering side effects.
Myositis means inflammation of the muscles. Two specific types are polymyositis and dermatomyositis. Read about myositis symptoms and management.
Myositis Awareness T-Shirt Where can I find other myositis awareness designs? Expand or collapse section. In addition to myositis awareness designs, you can explore the marketplace for myositis warrior, myositis, and myositis awareness month designs sold by independent artists. What material is this item made of? Expand or collapse section. 100% combed ringspun cotton. The perfect fabric for a graphic tee and the softest in the business. (Due to product availability, cotton type may vary for 2XL and 3XL sizes) Learn More » What USA ship methods are available? Expand or collapse section. Standard (6-8 Business Days) FedEx Air (4-6 Business Days) Estimates include printing and processing time. More Shipping Info » What is the Return/Exchange policy? Expand or collapse section. We want you to love your order! If for any reason you don't, let us know and we’ll make things right. Learn More »
Images, article and videos related to chronic pain and myositis pain.
Ways to alleviate the gastrointestinal and esophageal issues experienced by some people who have myositis.
ObjectiveCharacteristics of myositis with anti-Ku antibodies are poorly understood. The purpose of this study was to elucidate the pathologic features of myositis associated with anti-Ku antibodies, compared with immune-mediated necrotizing myopathy (IMNM)...
Sporadic inclusion body myositis (sIBM) is one of a group of rare muscle diseases called inflammatory myopathies, and is a progressive muscle disease characterized by muscle inflammation, weakness, and atrophy (muscle wasting).
Exercise resources, research, and videos for myositis patients. Exercise is recommended for myositis patients and is a treatment for inclusion body myositis.
Learn more about what lupus and myositis have in common as well as differences in symptoms, diagnosis, and treatment.
Autoimmune myopathies (IMs) are a group of diseases characterized by muscle weakness and inflammatory infiltrates on the muscle biopsy. `However, muscle in
Purpose of review—To review autoantibodies associated with different subtypes of idiopathic inflammatory myopathy (IIM) and their clinical applications. IIM are a heterogenous group of autoimmune disorders characterized by muscle weakness, cutaneous features, and internal organ involvement. The diagnosis and classification, which is often challenging, is made using a combination of clinical features, muscle enzyme levels, imaging, and biopsy. The landmark discoveries of novel autoantibodies specific to IIM subtypes have been one of the greatest advancements in the field of myositis. The specificity of these autoantibodies has simplified the diagnostic algorithm of IIM with their heterogenous presentation and outdated the earlier diagnostic criteria. Myositis-specific antibodies (MSAs) have improved diagnostics, clinical phenotyping, and prognostic stratification of the subtypes of IIMs. Furthermore, the levels of certain MSAs correlate with disease activity and muscle enzyme levels such that titers may be able to be used to predict disease course and treatment response.
