When an individual goes above and beyond, representing, raising awareness, and contributing financially to the work of The Myositis Association (TMA), it is more than fitting to present them with…
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How I moved from paralysis to hiking the Alps
Fiona Ratkoff is grateful to The Myositis Association for enabling her to get back on skis again after being paralyzed with dermatomyositis.
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Financial resources available
Myositis can make it hard to earn a living. Financial resources are available for qualified individuals. It never hurts to ask.
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Breaking news: Medicare coverage for power wheelchairs
TMA is excited to share the news about Medicare coverage for seat elevation for Medicare beneficiaries using power wheelchairs. The Centers for Medicare & Medicaid Services (CMS) has made a…
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The Myositis Association announces myositis research awards
COLUMBIA, MD, May 9, 2023 – The Myositis Association announces the awarding of two new research grants to fund basic and applied investigations in myositis diseases. Since 2002, TMA’s annual…
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